Search Genes

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            "gene_data": {
                "alias": [
                    "Spred-2",
                    "FLJ21897",
                    "FLJ31917"
                ],
                "biotype": "protein_coding",
                "hgnc_id": "HGNC:17722",
                "gene_name": "sprouty related EVH1 domain containing 2",
                "omim_gene": [
                    "609292"
                ],
                "alias_name": null,
                "gene_symbol": "SPRED2",
                "hgnc_symbol": "SPRED2",
                "hgnc_release": "2017-11-03",
                "ensembl_genes": {
                    "GRch37": {
                        "82": {
                            "location": "2:65537985-65659771",
                            "ensembl_id": "ENSG00000198369"
                        }
                    },
                    "GRch38": {
                        "90": {
                            "location": "2:65310851-65432637",
                            "ensembl_id": "ENSG00000198369"
                        }
                    }
                },
                "hgnc_date_symbol_changed": "2003-06-02"
            },
            "entity_type": "gene",
            "entity_name": "SPRED2",
            "confidence_level": "3",
            "penetrance": null,
            "mode_of_pathogenicity": null,
            "publications": [
                "PMID: 34626534"
            ],
            "evidence": [
                "Expert Review Green",
                "Literature"
            ],
            "phenotypes": [
                "Noonan syndrome 14, MIM# 619745"
            ],
            "mode_of_inheritance": "BIALLELIC, autosomal or pseudoautosomal",
            "tags": [],
            "panel": {
                "id": 3631,
                "hash_id": null,
                "name": "Growth failure",
                "disease_group": "",
                "disease_sub_group": "",
                "description": "This panel contains genes associated with growth failure in infancy/early childhood, either isolated or as part of another disorder.\r\n\r\nConsider applying this panel in individuals with:\r\n -Height Standard Deviation Score (SDS) <-3 (very significant short stature - well below the 0.4th centile)\r\nAND at least one of:\r\n- History of small for gestational age (birth weight and/or length <-2SDS)\r\n- Body disproportion, e.g. discrepancy between stature and head size\r\n- Dysmorphic features and congenital anomalies\r\n- Abnormalities in the GH-IGF axis (evidence of GH insensitivity or deficiency) and/or other pituitary hormonal deficiencies\r\n- Family history of significant short stature (1st and 2nd degree relatives) and/or consanguinity\r\n\r\nPrior to genomic testing consider:\r\n-Chromosomal microarray analysis (e.g. Turner syndrome)\r\n-Methylation analysis for Russell-Silver syndrome and Temple syndrome\r\n-Skeletal survey\r\n\r\nAcquired causes of short stature are relatively common.\r\n\r\nDepending on the specific clinical features present, consider applying the Skeletal dysplasia, Intellectual Disability, and/or Pituitary Hormone deficiency panels.\r\n\r\nWith thanks to Genomics England for the original design of this panel.",
                "status": "public",
                "version": "1.102",
                "version_created": "2026-04-01T10:17:12.005431+11:00",
                "relevant_disorders": [
                    "Failure to thrive",
                    "HP:0001508; Growth delay",
                    "HP:0001510"
                ],
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                    "number_of_strs": 0,
                    "number_of_regions": 4
                },
                "types": [
                    {
                        "name": "Victorian Clinical Genetics Services",
                        "slug": "victorian-clinical-genetics-services",
                        "description": "Panel used by VCGS."
                    },
                    {
                        "name": "Genetic Health Queensland",
                        "slug": "genetic-health-queensland",
                        "description": "Panel used by GHQ."
                    },
                    {
                        "name": "Royal Melbourne Hospital",
                        "slug": "royal-melbourne-hospital",
                        "description": "Royal Melbourne Hospital"
                    },
                    {
                        "name": "Rare Disease",
                        "slug": "rare-disease",
                        "description": "Rare disease panels"
                    }
                ],
                "child_panel_ids": []
            },
            "transcript": null
        },
        {
            "gene_data": {
                "alias": [
                    "BABL",
                    "LIPO"
                ],
                "biotype": "protein_coding",
                "hgnc_id": "HGNC:5009",
                "gene_name": "high mobility group AT-hook 2",
                "omim_gene": [
                    "600698"
                ],
                "alias_name": null,
                "gene_symbol": "HMGA2",
                "hgnc_symbol": "HMGA2",
                "hgnc_release": "2017-11-03",
                "ensembl_genes": {
                    "GRch37": {
                        "82": {
                            "location": "12:66217911-66360075",
                            "ensembl_id": "ENSG00000149948"
                        }
                    },
                    "GRch38": {
                        "90": {
                            "location": "12:65824131-65966295",
                            "ensembl_id": "ENSG00000149948"
                        }
                    }
                },
                "hgnc_date_symbol_changed": "2002-07-26"
            },
            "entity_type": "gene",
            "entity_name": "HMGA2",
            "confidence_level": "3",
            "penetrance": null,
            "mode_of_pathogenicity": "",
            "publications": [
                "25809938",
                "29453418",
                "29655892",
                "33482836"
            ],
            "evidence": [
                "Expert Review Green",
                "Genomics England PanelApp"
            ],
            "phenotypes": [
                "Silver-Russell syndrome 5, MIM# 618908",
                "MONDO:0020795"
            ],
            "mode_of_inheritance": "MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted",
            "tags": [],
            "panel": {
                "id": 3631,
                "hash_id": null,
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                "disease_group": "",
                "disease_sub_group": "",
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                "status": "public",
                "version": "1.102",
                "version_created": "2026-04-01T10:17:12.005431+11:00",
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                    "Failure to thrive",
                    "HP:0001508; Growth delay",
                    "HP:0001510"
                ],
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                },
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                    {
                        "name": "Victorian Clinical Genetics Services",
                        "slug": "victorian-clinical-genetics-services",
                        "description": "Panel used by VCGS."
                    },
                    {
                        "name": "Genetic Health Queensland",
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                    },
                    {
                        "name": "Royal Melbourne Hospital",
                        "slug": "royal-melbourne-hospital",
                        "description": "Royal Melbourne Hospital"
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                        "name": "Rare Disease",
                        "slug": "rare-disease",
                        "description": "Rare disease panels"
                    }
                ],
                "child_panel_ids": []
            },
            "transcript": null
        },
        {
            "gene_data": {
                "alias": [
                    "CEK2",
                    "JTK4",
                    "CD333"
                ],
                "biotype": "protein_coding",
                "hgnc_id": "HGNC:3690",
                "gene_name": "fibroblast growth factor receptor 3",
                "omim_gene": [
                    "134934"
                ],
                "alias_name": null,
                "gene_symbol": "FGFR3",
                "hgnc_symbol": "FGFR3",
                "hgnc_release": "2017-11-03",
                "ensembl_genes": {
                    "GRch37": {
                        "82": {
                            "location": "4:1795034-1810599",
                            "ensembl_id": "ENSG00000068078"
                        }
                    },
                    "GRch38": {
                        "90": {
                            "location": "4:1793307-1808872",
                            "ensembl_id": "ENSG00000068078"
                        }
                    }
                },
                "hgnc_date_symbol_changed": "1991-06-07"
            },
            "entity_type": "gene",
            "entity_name": "FGFR3",
            "confidence_level": "3",
            "penetrance": null,
            "mode_of_pathogenicity": "",
            "publications": [],
            "evidence": [
                "Expert Review Green",
                "Genomics England PanelApp"
            ],
            "phenotypes": [
                "Hypochondroplasia, MIM#146000"
            ],
            "mode_of_inheritance": "MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted",
            "tags": [],
            "panel": {
                "id": 3631,
                "hash_id": null,
                "name": "Growth failure",
                "disease_group": "",
                "disease_sub_group": "",
                "description": "This panel contains genes associated with growth failure in infancy/early childhood, either isolated or as part of another disorder.\r\n\r\nConsider applying this panel in individuals with:\r\n -Height Standard Deviation Score (SDS) <-3 (very significant short stature - well below the 0.4th centile)\r\nAND at least one of:\r\n- History of small for gestational age (birth weight and/or length <-2SDS)\r\n- Body disproportion, e.g. discrepancy between stature and head size\r\n- Dysmorphic features and congenital anomalies\r\n- Abnormalities in the GH-IGF axis (evidence of GH insensitivity or deficiency) and/or other pituitary hormonal deficiencies\r\n- Family history of significant short stature (1st and 2nd degree relatives) and/or consanguinity\r\n\r\nPrior to genomic testing consider:\r\n-Chromosomal microarray analysis (e.g. Turner syndrome)\r\n-Methylation analysis for Russell-Silver syndrome and Temple syndrome\r\n-Skeletal survey\r\n\r\nAcquired causes of short stature are relatively common.\r\n\r\nDepending on the specific clinical features present, consider applying the Skeletal dysplasia, Intellectual Disability, and/or Pituitary Hormone deficiency panels.\r\n\r\nWith thanks to Genomics England for the original design of this panel.",
                "status": "public",
                "version": "1.102",
                "version_created": "2026-04-01T10:17:12.005431+11:00",
                "relevant_disorders": [
                    "Failure to thrive",
                    "HP:0001508; Growth delay",
                    "HP:0001510"
                ],
                "stats": {
                    "number_of_genes": 204,
                    "number_of_strs": 0,
                    "number_of_regions": 4
                },
                "types": [
                    {
                        "name": "Victorian Clinical Genetics Services",
                        "slug": "victorian-clinical-genetics-services",
                        "description": "Panel used by VCGS."
                    },
                    {
                        "name": "Genetic Health Queensland",
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                        "description": "Panel used by GHQ."
                    },
                    {
                        "name": "Royal Melbourne Hospital",
                        "slug": "royal-melbourne-hospital",
                        "description": "Royal Melbourne Hospital"
                    },
                    {
                        "name": "Rare Disease",
                        "slug": "rare-disease",
                        "description": "Rare disease panels"
                    }
                ],
                "child_panel_ids": []
            },
            "transcript": null
        },
        {
            "gene_data": {
                "alias": [
                    "FLJ10719"
                ],
                "biotype": "protein_coding",
                "hgnc_id": "HGNC:25568",
                "gene_name": "Fanconi anemia complementation group I",
                "omim_gene": [
                    "611360"
                ],
                "alias_name": null,
                "gene_symbol": "FANCI",
                "hgnc_symbol": "FANCI",
                "hgnc_release": "2017-11-03",
                "ensembl_genes": {
                    "GRch37": {
                        "82": {
                            "location": "15:89787180-89860492",
                            "ensembl_id": "ENSG00000140525"
                        }
                    },
                    "GRch38": {
                        "90": {
                            "location": "15:89243949-89317261",
                            "ensembl_id": "ENSG00000140525"
                        }
                    }
                },
                "hgnc_date_symbol_changed": "2007-05-03"
            },
            "entity_type": "gene",
            "entity_name": "FANCI",
            "confidence_level": "3",
            "penetrance": null,
            "mode_of_pathogenicity": "",
            "publications": [
                "17452773",
                "11239453"
            ],
            "evidence": [
                "Expert Review Green",
                "Genomics England PanelApp",
                "Victorian Clinical Genetics Services"
            ],
            "phenotypes": [
                "Fanconi anemia, complementation group I, MIM# 609053",
                "MONDO:0012186"
            ],
            "mode_of_inheritance": "BIALLELIC, autosomal or pseudoautosomal",
            "tags": [],
            "panel": {
                "id": 3631,
                "hash_id": null,
                "name": "Growth failure",
                "disease_group": "",
                "disease_sub_group": "",
                "description": "This panel contains genes associated with growth failure in infancy/early childhood, either isolated or as part of another disorder.\r\n\r\nConsider applying this panel in individuals with:\r\n -Height Standard Deviation Score (SDS) <-3 (very significant short stature - well below the 0.4th centile)\r\nAND at least one of:\r\n- History of small for gestational age (birth weight and/or length <-2SDS)\r\n- Body disproportion, e.g. discrepancy between stature and head size\r\n- Dysmorphic features and congenital anomalies\r\n- Abnormalities in the GH-IGF axis (evidence of GH insensitivity or deficiency) and/or other pituitary hormonal deficiencies\r\n- Family history of significant short stature (1st and 2nd degree relatives) and/or consanguinity\r\n\r\nPrior to genomic testing consider:\r\n-Chromosomal microarray analysis (e.g. Turner syndrome)\r\n-Methylation analysis for Russell-Silver syndrome and Temple syndrome\r\n-Skeletal survey\r\n\r\nAcquired causes of short stature are relatively common.\r\n\r\nDepending on the specific clinical features present, consider applying the Skeletal dysplasia, Intellectual Disability, and/or Pituitary Hormone deficiency panels.\r\n\r\nWith thanks to Genomics England for the original design of this panel.",
                "status": "public",
                "version": "1.102",
                "version_created": "2026-04-01T10:17:12.005431+11:00",
                "relevant_disorders": [
                    "Failure to thrive",
                    "HP:0001508; Growth delay",
                    "HP:0001510"
                ],
                "stats": {
                    "number_of_genes": 204,
                    "number_of_strs": 0,
                    "number_of_regions": 4
                },
                "types": [
                    {
                        "name": "Victorian Clinical Genetics Services",
                        "slug": "victorian-clinical-genetics-services",
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                    },
                    {
                        "name": "Genetic Health Queensland",
                        "slug": "genetic-health-queensland",
                        "description": "Panel used by GHQ."
                    },
                    {
                        "name": "Royal Melbourne Hospital",
                        "slug": "royal-melbourne-hospital",
                        "description": "Royal Melbourne Hospital"
                    },
                    {
                        "name": "Rare Disease",
                        "slug": "rare-disease",
                        "description": "Rare disease panels"
                    }
                ],
                "child_panel_ids": []
            },
            "transcript": null
        },
        {
            "gene_data": {
                "alias": [
                    "FAG"
                ],
                "biotype": "protein_coding",
                "hgnc_id": "HGNC:3588",
                "gene_name": "Fanconi anemia complementation group G",
                "omim_gene": [
                    "602956"
                ],
                "alias_name": [
                    "DNA repair protein XRCC9",
                    "X-ray repair, complementing defective, in Chinese hamster, 9",
                    "X-ray repair complementing defective repair in Chinese hamster cells 9"
                ],
                "gene_symbol": "FANCG",
                "hgnc_symbol": "FANCG",
                "hgnc_release": "2017-11-03",
                "ensembl_genes": {
                    "GRch37": {
                        "82": {
                            "location": "9:35073832-35080013",
                            "ensembl_id": "ENSG00000221829"
                        }
                    },
                    "GRch38": {
                        "90": {
                            "location": "9:35073835-35080016",
                            "ensembl_id": "ENSG00000221829"
                        }
                    }
                },
                "hgnc_date_symbol_changed": "1998-08-26"
            },
            "entity_type": "gene",
            "entity_name": "FANCG",
            "confidence_level": "3",
            "penetrance": null,
            "mode_of_pathogenicity": "",
            "publications": [
                "16493006",
                "9806548",
                "9806548",
                "12552564"
            ],
            "evidence": [
                "Expert Review Green",
                "Genomics England PanelApp",
                "Victorian Clinical Genetics Services"
            ],
            "phenotypes": [
                "Fanconi anaemia, complementation group G, MIM# 614082",
                "MONDO:0013565"
            ],
            "mode_of_inheritance": "BIALLELIC, autosomal or pseudoautosomal",
            "tags": [],
            "panel": {
                "id": 3631,
                "hash_id": null,
                "name": "Growth failure",
                "disease_group": "",
                "disease_sub_group": "",
                "description": "This panel contains genes associated with growth failure in infancy/early childhood, either isolated or as part of another disorder.\r\n\r\nConsider applying this panel in individuals with:\r\n -Height Standard Deviation Score (SDS) <-3 (very significant short stature - well below the 0.4th centile)\r\nAND at least one of:\r\n- History of small for gestational age (birth weight and/or length <-2SDS)\r\n- Body disproportion, e.g. discrepancy between stature and head size\r\n- Dysmorphic features and congenital anomalies\r\n- Abnormalities in the GH-IGF axis (evidence of GH insensitivity or deficiency) and/or other pituitary hormonal deficiencies\r\n- Family history of significant short stature (1st and 2nd degree relatives) and/or consanguinity\r\n\r\nPrior to genomic testing consider:\r\n-Chromosomal microarray analysis (e.g. Turner syndrome)\r\n-Methylation analysis for Russell-Silver syndrome and Temple syndrome\r\n-Skeletal survey\r\n\r\nAcquired causes of short stature are relatively common.\r\n\r\nDepending on the specific clinical features present, consider applying the Skeletal dysplasia, Intellectual Disability, and/or Pituitary Hormone deficiency panels.\r\n\r\nWith thanks to Genomics England for the original design of this panel.",
                "status": "public",
                "version": "1.102",
                "version_created": "2026-04-01T10:17:12.005431+11:00",
                "relevant_disorders": [
                    "Failure to thrive",
                    "HP:0001508; Growth delay",
                    "HP:0001510"
                ],
                "stats": {
                    "number_of_genes": 204,
                    "number_of_strs": 0,
                    "number_of_regions": 4
                },
                "types": [
                    {
                        "name": "Victorian Clinical Genetics Services",
                        "slug": "victorian-clinical-genetics-services",
                        "description": "Panel used by VCGS."
                    },
                    {
                        "name": "Genetic Health Queensland",
                        "slug": "genetic-health-queensland",
                        "description": "Panel used by GHQ."
                    },
                    {
                        "name": "Royal Melbourne Hospital",
                        "slug": "royal-melbourne-hospital",
                        "description": "Royal Melbourne Hospital"
                    },
                    {
                        "name": "Rare Disease",
                        "slug": "rare-disease",
                        "description": "Rare disease panels"
                    }
                ],
                "child_panel_ids": []
            },
            "transcript": null
        },
        {
            "gene_data": {
                "alias": [
                    "TEM8",
                    "FLJ21776",
                    "FLJ10601",
                    "ATR"
                ],
                "biotype": "protein_coding",
                "hgnc_id": "HGNC:21014",
                "gene_name": "anthrax toxin receptor 1",
                "omim_gene": [
                    "606410"
                ],
                "alias_name": [
                    "anthrax toxin receptor",
                    "tumor endothelial marker 8 precursor"
                ],
                "gene_symbol": "ANTXR1",
                "hgnc_symbol": "ANTXR1",
                "hgnc_release": "2017-11-03",
                "ensembl_genes": {
                    "GRch37": {
                        "82": {
                            "location": "2:69240310-69476459",
                            "ensembl_id": "ENSG00000169604"
                        }
                    },
                    "GRch38": {
                        "90": {
                            "location": "2:69013178-69249327",
                            "ensembl_id": "ENSG00000169604"
                        }
                    }
                },
                "hgnc_date_symbol_changed": "2003-08-27"
            },
            "entity_type": "gene",
            "entity_name": "ANTXR1",
            "confidence_level": "3",
            "penetrance": null,
            "mode_of_pathogenicity": null,
            "publications": [
                "23602711",
                "25045128",
                "31425299",
                "30575274",
                "29436111",
                "28870703"
            ],
            "evidence": [
                "Expert Review Green",
                "Expert Review"
            ],
            "phenotypes": [
                "GAPO syndrome, MIM# 230740"
            ],
            "mode_of_inheritance": "BIALLELIC, autosomal or pseudoautosomal",
            "tags": [],
            "panel": {
                "id": 3631,
                "hash_id": null,
                "name": "Growth failure",
                "disease_group": "",
                "disease_sub_group": "",
                "description": "This panel contains genes associated with growth failure in infancy/early childhood, either isolated or as part of another disorder.\r\n\r\nConsider applying this panel in individuals with:\r\n -Height Standard Deviation Score (SDS) <-3 (very significant short stature - well below the 0.4th centile)\r\nAND at least one of:\r\n- History of small for gestational age (birth weight and/or length <-2SDS)\r\n- Body disproportion, e.g. discrepancy between stature and head size\r\n- Dysmorphic features and congenital anomalies\r\n- Abnormalities in the GH-IGF axis (evidence of GH insensitivity or deficiency) and/or other pituitary hormonal deficiencies\r\n- Family history of significant short stature (1st and 2nd degree relatives) and/or consanguinity\r\n\r\nPrior to genomic testing consider:\r\n-Chromosomal microarray analysis (e.g. Turner syndrome)\r\n-Methylation analysis for Russell-Silver syndrome and Temple syndrome\r\n-Skeletal survey\r\n\r\nAcquired causes of short stature are relatively common.\r\n\r\nDepending on the specific clinical features present, consider applying the Skeletal dysplasia, Intellectual Disability, and/or Pituitary Hormone deficiency panels.\r\n\r\nWith thanks to Genomics England for the original design of this panel.",
                "status": "public",
                "version": "1.102",
                "version_created": "2026-04-01T10:17:12.005431+11:00",
                "relevant_disorders": [
                    "Failure to thrive",
                    "HP:0001508; Growth delay",
                    "HP:0001510"
                ],
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                    "number_of_regions": 4
                },
                "types": [
                    {
                        "name": "Victorian Clinical Genetics Services",
                        "slug": "victorian-clinical-genetics-services",
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                    },
                    {
                        "name": "Genetic Health Queensland",
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                    },
                    {
                        "name": "Royal Melbourne Hospital",
                        "slug": "royal-melbourne-hospital",
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                    },
                    {
                        "name": "Rare Disease",
                        "slug": "rare-disease",
                        "description": "Rare disease panels"
                    }
                ],
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            },
            "transcript": []
        },
        {
            "gene_data": {
                "alias": [],
                "biotype": "protein_coding",
                "hgnc_id": "HGNC:1739",
                "gene_name": "cell division cycle 45",
                "omim_gene": [
                    "603465"
                ],
                "alias_name": [
                    "human CDC45"
                ],
                "gene_symbol": "CDC45",
                "hgnc_symbol": "CDC45",
                "hgnc_release": "2017-11-03",
                "ensembl_genes": {
                    "GRch37": {
                        "82": {
                            "location": "22:19466982-19508135",
                            "ensembl_id": "ENSG00000093009"
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                    "GRch38": {
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                            "location": "22:19479459-19520612",
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                    }
                },
                "hgnc_date_symbol_changed": "2010-03-24"
            },
            "entity_type": "gene",
            "entity_name": "CDC45",
            "confidence_level": "3",
            "penetrance": null,
            "mode_of_pathogenicity": null,
            "publications": [
                "31474763",
                "27374770"
            ],
            "evidence": [
                "Expert Review Green",
                "Expert Review"
            ],
            "phenotypes": [
                "Meier-Gorlin syndrome 7, MIM 617063"
            ],
            "mode_of_inheritance": "BIALLELIC, autosomal or pseudoautosomal",
            "tags": [],
            "panel": {
                "id": 3631,
                "hash_id": null,
                "name": "Growth failure",
                "disease_group": "",
                "disease_sub_group": "",
                "description": "This panel contains genes associated with growth failure in infancy/early childhood, either isolated or as part of another disorder.\r\n\r\nConsider applying this panel in individuals with:\r\n -Height Standard Deviation Score (SDS) <-3 (very significant short stature - well below the 0.4th centile)\r\nAND at least one of:\r\n- History of small for gestational age (birth weight and/or length <-2SDS)\r\n- Body disproportion, e.g. discrepancy between stature and head size\r\n- Dysmorphic features and congenital anomalies\r\n- Abnormalities in the GH-IGF axis (evidence of GH insensitivity or deficiency) and/or other pituitary hormonal deficiencies\r\n- Family history of significant short stature (1st and 2nd degree relatives) and/or consanguinity\r\n\r\nPrior to genomic testing consider:\r\n-Chromosomal microarray analysis (e.g. Turner syndrome)\r\n-Methylation analysis for Russell-Silver syndrome and Temple syndrome\r\n-Skeletal survey\r\n\r\nAcquired causes of short stature are relatively common.\r\n\r\nDepending on the specific clinical features present, consider applying the Skeletal dysplasia, Intellectual Disability, and/or Pituitary Hormone deficiency panels.\r\n\r\nWith thanks to Genomics England for the original design of this panel.",
                "status": "public",
                "version": "1.102",
                "version_created": "2026-04-01T10:17:12.005431+11:00",
                "relevant_disorders": [
                    "Failure to thrive",
                    "HP:0001508; Growth delay",
                    "HP:0001510"
                ],
                "stats": {
                    "number_of_genes": 204,
                    "number_of_strs": 0,
                    "number_of_regions": 4
                },
                "types": [
                    {
                        "name": "Victorian Clinical Genetics Services",
                        "slug": "victorian-clinical-genetics-services",
                        "description": "Panel used by VCGS."
                    },
                    {
                        "name": "Genetic Health Queensland",
                        "slug": "genetic-health-queensland",
                        "description": "Panel used by GHQ."
                    },
                    {
                        "name": "Royal Melbourne Hospital",
                        "slug": "royal-melbourne-hospital",
                        "description": "Royal Melbourne Hospital"
                    },
                    {
                        "name": "Rare Disease",
                        "slug": "rare-disease",
                        "description": "Rare disease panels"
                    }
                ],
                "child_panel_ids": []
            },
            "transcript": []
        },
        {
            "gene_data": {
                "alias": [
                    "KRAS1"
                ],
                "biotype": "protein_coding",
                "hgnc_id": "HGNC:6407",
                "gene_name": "KRAS proto-oncogene, GTPase",
                "omim_gene": [
                    "190070"
                ],
                "alias_name": null,
                "gene_symbol": "KRAS",
                "hgnc_symbol": "KRAS",
                "hgnc_release": "2017-11-03",
                "ensembl_genes": {
                    "GRch37": {
                        "82": {
                            "location": "12:25357723-25403870",
                            "ensembl_id": "ENSG00000133703"
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                    },
                    "GRch38": {
                        "90": {
                            "location": "12:25204789-25250936",
                            "ensembl_id": "ENSG00000133703"
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                    }
                },
                "hgnc_date_symbol_changed": "2005-01-24"
            },
            "entity_type": "gene",
            "entity_name": "KRAS",
            "confidence_level": "3",
            "penetrance": null,
            "mode_of_pathogenicity": "Loss-of-function variants (as defined in pop up message) DO NOT cause this phenotype - please provide details in the comments",
            "publications": [
                "21396583",
                "21797849",
                "16474404",
                "16474405",
                "16773572",
                "17056636"
            ],
            "evidence": [
                "Expert Review Green",
                "Genomics England PanelApp",
                "Victorian Clinical Genetics Services"
            ],
            "phenotypes": [
                "Noonan syndrome 3, MIM# 609942",
                "Cardiofaciocutaneous syndrome 2, MIM# 615278"
            ],
            "mode_of_inheritance": "MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted",
            "tags": [],
            "panel": {
                "id": 3631,
                "hash_id": null,
                "name": "Growth failure",
                "disease_group": "",
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                "description": "This panel contains genes associated with growth failure in infancy/early childhood, either isolated or as part of another disorder.\r\n\r\nConsider applying this panel in individuals with:\r\n -Height Standard Deviation Score (SDS) <-3 (very significant short stature - well below the 0.4th centile)\r\nAND at least one of:\r\n- History of small for gestational age (birth weight and/or length <-2SDS)\r\n- Body disproportion, e.g. discrepancy between stature and head size\r\n- Dysmorphic features and congenital anomalies\r\n- Abnormalities in the GH-IGF axis (evidence of GH insensitivity or deficiency) and/or other pituitary hormonal deficiencies\r\n- Family history of significant short stature (1st and 2nd degree relatives) and/or consanguinity\r\n\r\nPrior to genomic testing consider:\r\n-Chromosomal microarray analysis (e.g. Turner syndrome)\r\n-Methylation analysis for Russell-Silver syndrome and Temple syndrome\r\n-Skeletal survey\r\n\r\nAcquired causes of short stature are relatively common.\r\n\r\nDepending on the specific clinical features present, consider applying the Skeletal dysplasia, Intellectual Disability, and/or Pituitary Hormone deficiency panels.\r\n\r\nWith thanks to Genomics England for the original design of this panel.",
                "status": "public",
                "version": "1.102",
                "version_created": "2026-04-01T10:17:12.005431+11:00",
                "relevant_disorders": [
                    "Failure to thrive",
                    "HP:0001508; Growth delay",
                    "HP:0001510"
                ],
                "stats": {
                    "number_of_genes": 204,
                    "number_of_strs": 0,
                    "number_of_regions": 4
                },
                "types": [
                    {
                        "name": "Victorian Clinical Genetics Services",
                        "slug": "victorian-clinical-genetics-services",
                        "description": "Panel used by VCGS."
                    },
                    {
                        "name": "Genetic Health Queensland",
                        "slug": "genetic-health-queensland",
                        "description": "Panel used by GHQ."
                    },
                    {
                        "name": "Royal Melbourne Hospital",
                        "slug": "royal-melbourne-hospital",
                        "description": "Royal Melbourne Hospital"
                    },
                    {
                        "name": "Rare Disease",
                        "slug": "rare-disease",
                        "description": "Rare disease panels"
                    }
                ],
                "child_panel_ids": []
            },
            "transcript": null
        },
        {
            "gene_data": {
                "alias": [
                    "RNF113",
                    "Cwc24"
                ],
                "biotype": "protein_coding",
                "hgnc_id": "HGNC:12974",
                "gene_name": "ring finger protein 113A",
                "omim_gene": [
                    "300951"
                ],
                "alias_name": null,
                "gene_symbol": "RNF113A",
                "hgnc_symbol": "RNF113A",
                "hgnc_release": "2017-11-03",
                "ensembl_genes": {
                    "GRch37": {
                        "82": {
                            "location": "X:119004497-119005791",
                            "ensembl_id": "ENSG00000125352"
                        }
                    },
                    "GRch38": {
                        "90": {
                            "location": "X:119870475-119871827",
                            "ensembl_id": "ENSG00000125352"
                        }
                    }
                },
                "hgnc_date_symbol_changed": "2005-03-22"
            },
            "entity_type": "gene",
            "entity_name": "RNF113A",
            "confidence_level": "3",
            "penetrance": null,
            "mode_of_pathogenicity": null,
            "publications": [
                "25612912",
                "31793730",
                "31880405"
            ],
            "evidence": [
                "Expert Review Green",
                "Expert Review"
            ],
            "phenotypes": [
                "Trichothiodystrophy 5, nonphotosensitive",
                "OMIM #300953"
            ],
            "mode_of_inheritance": "X-LINKED: hemizygous mutation in males, biallelic mutations in females",
            "tags": [],
            "panel": {
                "id": 3631,
                "hash_id": null,
                "name": "Growth failure",
                "disease_group": "",
                "disease_sub_group": "",
                "description": "This panel contains genes associated with growth failure in infancy/early childhood, either isolated or as part of another disorder.\r\n\r\nConsider applying this panel in individuals with:\r\n -Height Standard Deviation Score (SDS) <-3 (very significant short stature - well below the 0.4th centile)\r\nAND at least one of:\r\n- History of small for gestational age (birth weight and/or length <-2SDS)\r\n- Body disproportion, e.g. discrepancy between stature and head size\r\n- Dysmorphic features and congenital anomalies\r\n- Abnormalities in the GH-IGF axis (evidence of GH insensitivity or deficiency) and/or other pituitary hormonal deficiencies\r\n- Family history of significant short stature (1st and 2nd degree relatives) and/or consanguinity\r\n\r\nPrior to genomic testing consider:\r\n-Chromosomal microarray analysis (e.g. Turner syndrome)\r\n-Methylation analysis for Russell-Silver syndrome and Temple syndrome\r\n-Skeletal survey\r\n\r\nAcquired causes of short stature are relatively common.\r\n\r\nDepending on the specific clinical features present, consider applying the Skeletal dysplasia, Intellectual Disability, and/or Pituitary Hormone deficiency panels.\r\n\r\nWith thanks to Genomics England for the original design of this panel.",
                "status": "public",
                "version": "1.102",
                "version_created": "2026-04-01T10:17:12.005431+11:00",
                "relevant_disorders": [
                    "Failure to thrive",
                    "HP:0001508; Growth delay",
                    "HP:0001510"
                ],
                "stats": {
                    "number_of_genes": 204,
                    "number_of_strs": 0,
                    "number_of_regions": 4
                },
                "types": [
                    {
                        "name": "Victorian Clinical Genetics Services",
                        "slug": "victorian-clinical-genetics-services",
                        "description": "Panel used by VCGS."
                    },
                    {
                        "name": "Genetic Health Queensland",
                        "slug": "genetic-health-queensland",
                        "description": "Panel used by GHQ."
                    },
                    {
                        "name": "Royal Melbourne Hospital",
                        "slug": "royal-melbourne-hospital",
                        "description": "Royal Melbourne Hospital"
                    },
                    {
                        "name": "Rare Disease",
                        "slug": "rare-disease",
                        "description": "Rare disease panels"
                    }
                ],
                "child_panel_ids": []
            },
            "transcript": []
        },
        {
            "gene_data": {
                "alias": [
                    "TRX1",
                    "HRX",
                    "ALL-1",
                    "HTRX1",
                    "CXXC7",
                    "MLL1A"
                ],
                "biotype": "protein_coding",
                "hgnc_id": "HGNC:7132",
                "gene_name": "lysine methyltransferase 2A",
                "omim_gene": [
                    "159555"
                ],
                "alias_name": null,
                "gene_symbol": "KMT2A",
                "hgnc_symbol": "KMT2A",
                "hgnc_release": "2017-11-03",
                "ensembl_genes": {
                    "GRch37": {
                        "82": {
                            "location": "11:118307205-118397539",
                            "ensembl_id": "ENSG00000118058"
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                    },
                    "GRch38": {
                        "90": {
                            "location": "11:118436490-118526832",
                            "ensembl_id": "ENSG00000118058"
                        }
                    }
                },
                "hgnc_date_symbol_changed": "2013-05-09"
            },
            "entity_type": "gene",
            "entity_name": "KMT2A",
            "confidence_level": "3",
            "penetrance": null,
            "mode_of_pathogenicity": null,
            "publications": [
                "22795537",
                "25810209",
                "29574747",
                "33783954"
            ],
            "evidence": [
                "Expert Review Green",
                "Literature"
            ],
            "phenotypes": [
                "Wiedemann-Steiner syndrome",
                "OMIM #605130"
            ],
            "mode_of_inheritance": "MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted",
            "tags": [],
            "panel": {
                "id": 3631,
                "hash_id": null,
                "name": "Growth failure",
                "disease_group": "",
                "disease_sub_group": "",
                "description": "This panel contains genes associated with growth failure in infancy/early childhood, either isolated or as part of another disorder.\r\n\r\nConsider applying this panel in individuals with:\r\n -Height Standard Deviation Score (SDS) <-3 (very significant short stature - well below the 0.4th centile)\r\nAND at least one of:\r\n- History of small for gestational age (birth weight and/or length <-2SDS)\r\n- Body disproportion, e.g. discrepancy between stature and head size\r\n- Dysmorphic features and congenital anomalies\r\n- Abnormalities in the GH-IGF axis (evidence of GH insensitivity or deficiency) and/or other pituitary hormonal deficiencies\r\n- Family history of significant short stature (1st and 2nd degree relatives) and/or consanguinity\r\n\r\nPrior to genomic testing consider:\r\n-Chromosomal microarray analysis (e.g. Turner syndrome)\r\n-Methylation analysis for Russell-Silver syndrome and Temple syndrome\r\n-Skeletal survey\r\n\r\nAcquired causes of short stature are relatively common.\r\n\r\nDepending on the specific clinical features present, consider applying the Skeletal dysplasia, Intellectual Disability, and/or Pituitary Hormone deficiency panels.\r\n\r\nWith thanks to Genomics England for the original design of this panel.",
                "status": "public",
                "version": "1.102",
                "version_created": "2026-04-01T10:17:12.005431+11:00",
                "relevant_disorders": [
                    "Failure to thrive",
                    "HP:0001508; Growth delay",
                    "HP:0001510"
                ],
                "stats": {
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                    "number_of_strs": 0,
                    "number_of_regions": 4
                },
                "types": [
                    {
                        "name": "Victorian Clinical Genetics Services",
                        "slug": "victorian-clinical-genetics-services",
                        "description": "Panel used by VCGS."
                    },
                    {
                        "name": "Genetic Health Queensland",
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                        "description": "Panel used by GHQ."
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                    {
                        "name": "Royal Melbourne Hospital",
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                    {
                        "name": "Rare Disease",
                        "slug": "rare-disease",
                        "description": "Rare disease panels"
                    }
                ],
                "child_panel_ids": []
            },
            "transcript": []
        },
        {
            "gene_data": {
                "alias": [
                    "FLJ44734",
                    "IGF-II"
                ],
                "biotype": "protein_coding",
                "hgnc_id": "HGNC:5466",
                "gene_name": "insulin like growth factor 2",
                "omim_gene": [
                    "147470"
                ],
                "alias_name": [
                    "somatomedin A",
                    "preptin"
                ],
                "gene_symbol": "IGF2",
                "hgnc_symbol": "IGF2",
                "hgnc_release": "2017-11-03",
                "ensembl_genes": {
                    "GRch37": {
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                            "location": "11:2150342-2170833",
                            "ensembl_id": "ENSG00000167244"
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                    },
                    "GRch38": {
                        "90": {
                            "location": "11:2129112-2141238",
                            "ensembl_id": "ENSG00000167244"
                        }
                    }
                },
                "hgnc_date_symbol_changed": "2001-06-22"
            },
            "entity_type": "gene",
            "entity_name": "IGF2",
            "confidence_level": "3",
            "penetrance": null,
            "mode_of_pathogenicity": "",
            "publications": [
                "26154720",
                "31544945"
            ],
            "evidence": [
                "Expert Review Green",
                "Genomics England PanelApp"
            ],
            "phenotypes": [
                "Silver-Russell syndrome 3, MIM #616489"
            ],
            "mode_of_inheritance": "MONOALLELIC, autosomal or pseudoautosomal, maternally imprinted (paternal allele expressed)",
            "tags": [],
            "panel": {
                "id": 3631,
                "hash_id": null,
                "name": "Growth failure",
                "disease_group": "",
                "disease_sub_group": "",
                "description": "This panel contains genes associated with growth failure in infancy/early childhood, either isolated or as part of another disorder.\r\n\r\nConsider applying this panel in individuals with:\r\n -Height Standard Deviation Score (SDS) <-3 (very significant short stature - well below the 0.4th centile)\r\nAND at least one of:\r\n- History of small for gestational age (birth weight and/or length <-2SDS)\r\n- Body disproportion, e.g. discrepancy between stature and head size\r\n- Dysmorphic features and congenital anomalies\r\n- Abnormalities in the GH-IGF axis (evidence of GH insensitivity or deficiency) and/or other pituitary hormonal deficiencies\r\n- Family history of significant short stature (1st and 2nd degree relatives) and/or consanguinity\r\n\r\nPrior to genomic testing consider:\r\n-Chromosomal microarray analysis (e.g. Turner syndrome)\r\n-Methylation analysis for Russell-Silver syndrome and Temple syndrome\r\n-Skeletal survey\r\n\r\nAcquired causes of short stature are relatively common.\r\n\r\nDepending on the specific clinical features present, consider applying the Skeletal dysplasia, Intellectual Disability, and/or Pituitary Hormone deficiency panels.\r\n\r\nWith thanks to Genomics England for the original design of this panel.",
                "status": "public",
                "version": "1.102",
                "version_created": "2026-04-01T10:17:12.005431+11:00",
                "relevant_disorders": [
                    "Failure to thrive",
                    "HP:0001508; Growth delay",
                    "HP:0001510"
                ],
                "stats": {
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                    "number_of_strs": 0,
                    "number_of_regions": 4
                },
                "types": [
                    {
                        "name": "Victorian Clinical Genetics Services",
                        "slug": "victorian-clinical-genetics-services",
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                    },
                    {
                        "name": "Genetic Health Queensland",
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                    {
                        "name": "Royal Melbourne Hospital",
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                    },
                    {
                        "name": "Rare Disease",
                        "slug": "rare-disease",
                        "description": "Rare disease panels"
                    }
                ],
                "child_panel_ids": []
            },
            "transcript": null
        },
        {
            "gene_data": {
                "alias": [
                    "FLJ13479"
                ],
                "biotype": "protein_coding",
                "hgnc_id": "HGNC:25821",
                "gene_name": "zinc finger protein 668",
                "omim_gene": [
                    "617103"
                ],
                "alias_name": null,
                "gene_symbol": "ZNF668",
                "hgnc_symbol": "ZNF668",
                "hgnc_release": "2017-11-03",
                "ensembl_genes": {
                    "GRch37": {
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                            "location": "16:31072164-31085641",
                            "ensembl_id": "ENSG00000167394"
                        }
                    },
                    "GRch38": {
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                            "location": "16:31060843-31074320",
                            "ensembl_id": "ENSG00000167394"
                        }
                    }
                },
                "hgnc_date_symbol_changed": "2005-03-18"
            },
            "entity_type": "gene",
            "entity_name": "ZNF668",
            "confidence_level": "2",
            "penetrance": null,
            "mode_of_pathogenicity": null,
            "publications": [
                "34313816",
                "26633546"
            ],
            "evidence": [
                "Expert Review Amber",
                "Literature"
            ],
            "phenotypes": [
                "Neurodevelopmental disorder with poor growth, large ears, and dysmorphic facies, MIM# 620194"
            ],
            "mode_of_inheritance": "BIALLELIC, autosomal or pseudoautosomal",
            "tags": [],
            "panel": {
                "id": 3631,
                "hash_id": null,
                "name": "Growth failure",
                "disease_group": "",
                "disease_sub_group": "",
                "description": "This panel contains genes associated with growth failure in infancy/early childhood, either isolated or as part of another disorder.\r\n\r\nConsider applying this panel in individuals with:\r\n -Height Standard Deviation Score (SDS) <-3 (very significant short stature - well below the 0.4th centile)\r\nAND at least one of:\r\n- History of small for gestational age (birth weight and/or length <-2SDS)\r\n- Body disproportion, e.g. discrepancy between stature and head size\r\n- Dysmorphic features and congenital anomalies\r\n- Abnormalities in the GH-IGF axis (evidence of GH insensitivity or deficiency) and/or other pituitary hormonal deficiencies\r\n- Family history of significant short stature (1st and 2nd degree relatives) and/or consanguinity\r\n\r\nPrior to genomic testing consider:\r\n-Chromosomal microarray analysis (e.g. Turner syndrome)\r\n-Methylation analysis for Russell-Silver syndrome and Temple syndrome\r\n-Skeletal survey\r\n\r\nAcquired causes of short stature are relatively common.\r\n\r\nDepending on the specific clinical features present, consider applying the Skeletal dysplasia, Intellectual Disability, and/or Pituitary Hormone deficiency panels.\r\n\r\nWith thanks to Genomics England for the original design of this panel.",
                "status": "public",
                "version": "1.102",
                "version_created": "2026-04-01T10:17:12.005431+11:00",
                "relevant_disorders": [
                    "Failure to thrive",
                    "HP:0001508; Growth delay",
                    "HP:0001510"
                ],
                "stats": {
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                    "number_of_strs": 0,
                    "number_of_regions": 4
                },
                "types": [
                    {
                        "name": "Victorian Clinical Genetics Services",
                        "slug": "victorian-clinical-genetics-services",
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                    },
                    {
                        "name": "Genetic Health Queensland",
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                    {
                        "name": "Royal Melbourne Hospital",
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                    },
                    {
                        "name": "Rare Disease",
                        "slug": "rare-disease",
                        "description": "Rare disease panels"
                    }
                ],
                "child_panel_ids": []
            },
            "transcript": null
        },
        {
            "gene_data": {
                "alias": [
                    "PSF2",
                    "Pfs2"
                ],
                "biotype": "protein_coding",
                "hgnc_id": "HGNC:24575",
                "gene_name": "GINS complex subunit 2",
                "omim_gene": [
                    "610609"
                ],
                "alias_name": null,
                "gene_symbol": "GINS2",
                "hgnc_symbol": "GINS2",
                "hgnc_release": "2017-11-03",
                "ensembl_genes": {
                    "GRch37": {
                        "82": {
                            "location": "16:85709804-85723679",
                            "ensembl_id": "ENSG00000131153"
                        }
                    },
                    "GRch38": {
                        "90": {
                            "location": "16:85676198-85690073",
                            "ensembl_id": "ENSG00000131153"
                        }
                    }
                },
                "hgnc_date_symbol_changed": "2006-05-04"
            },
            "entity_type": "gene",
            "entity_name": "GINS2",
            "confidence_level": "1",
            "penetrance": null,
            "mode_of_pathogenicity": null,
            "publications": [
                "34353863"
            ],
            "evidence": [
                "Expert Review Red",
                "Literature"
            ],
            "phenotypes": [
                "Meier-Gorlin syndrome with craniosynostosis"
            ],
            "mode_of_inheritance": "BIALLELIC, autosomal or pseudoautosomal",
            "tags": [],
            "panel": {
                "id": 3631,
                "hash_id": null,
                "name": "Growth failure",
                "disease_group": "",
                "disease_sub_group": "",
                "description": "This panel contains genes associated with growth failure in infancy/early childhood, either isolated or as part of another disorder.\r\n\r\nConsider applying this panel in individuals with:\r\n -Height Standard Deviation Score (SDS) <-3 (very significant short stature - well below the 0.4th centile)\r\nAND at least one of:\r\n- History of small for gestational age (birth weight and/or length <-2SDS)\r\n- Body disproportion, e.g. discrepancy between stature and head size\r\n- Dysmorphic features and congenital anomalies\r\n- Abnormalities in the GH-IGF axis (evidence of GH insensitivity or deficiency) and/or other pituitary hormonal deficiencies\r\n- Family history of significant short stature (1st and 2nd degree relatives) and/or consanguinity\r\n\r\nPrior to genomic testing consider:\r\n-Chromosomal microarray analysis (e.g. Turner syndrome)\r\n-Methylation analysis for Russell-Silver syndrome and Temple syndrome\r\n-Skeletal survey\r\n\r\nAcquired causes of short stature are relatively common.\r\n\r\nDepending on the specific clinical features present, consider applying the Skeletal dysplasia, Intellectual Disability, and/or Pituitary Hormone deficiency panels.\r\n\r\nWith thanks to Genomics England for the original design of this panel.",
                "status": "public",
                "version": "1.102",
                "version_created": "2026-04-01T10:17:12.005431+11:00",
                "relevant_disorders": [
                    "Failure to thrive",
                    "HP:0001508; Growth delay",
                    "HP:0001510"
                ],
                "stats": {
                    "number_of_genes": 204,
                    "number_of_strs": 0,
                    "number_of_regions": 4
                },
                "types": [
                    {
                        "name": "Victorian Clinical Genetics Services",
                        "slug": "victorian-clinical-genetics-services",
                        "description": "Panel used by VCGS."
                    },
                    {
                        "name": "Genetic Health Queensland",
                        "slug": "genetic-health-queensland",
                        "description": "Panel used by GHQ."
                    },
                    {
                        "name": "Royal Melbourne Hospital",
                        "slug": "royal-melbourne-hospital",
                        "description": "Royal Melbourne Hospital"
                    },
                    {
                        "name": "Rare Disease",
                        "slug": "rare-disease",
                        "description": "Rare disease panels"
                    }
                ],
                "child_panel_ids": []
            },
            "transcript": []
        },
        {
            "gene_data": {
                "alias": [
                    "APRF"
                ],
                "biotype": "protein_coding",
                "hgnc_id": "HGNC:11364",
                "gene_name": "signal transducer and activator of transcription 3",
                "omim_gene": [
                    "102582"
                ],
                "alias_name": null,
                "gene_symbol": "STAT3",
                "hgnc_symbol": "STAT3",
                "hgnc_release": "2017-11-03",
                "ensembl_genes": {
                    "GRch37": {
                        "82": {
                            "location": "17:40465342-40540586",
                            "ensembl_id": "ENSG00000168610"
                        }
                    },
                    "GRch38": {
                        "90": {
                            "location": "17:42313324-42388568",
                            "ensembl_id": "ENSG00000168610"
                        }
                    }
                },
                "hgnc_date_symbol_changed": "1995-11-08"
            },
            "entity_type": "gene",
            "entity_name": "STAT3",
            "confidence_level": "3",
            "penetrance": null,
            "mode_of_pathogenicity": "Loss-of-function variants (as defined in pop up message) DO NOT cause this phenotype - please provide details in the comments",
            "publications": [
                "25349174",
                "25038750",
                "25359994"
            ],
            "evidence": [
                "Expert Review Green",
                "Literature"
            ],
            "phenotypes": [
                "Autoimmune disease, multisystem, infantile-onset, 1 MIM# 615952",
                "Lymphoproliferation",
                "solid organ autoimmunity",
                "growth failure",
                "recurrent infections",
                "short stature",
                "IUGR",
                "eczema",
                "delayed puberty",
                "dental abnormalities",
                "autoimmune interstitial lung disease",
                "juvenile-onset arthritis",
                "primary hypothyroidism"
            ],
            "mode_of_inheritance": "MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted",
            "tags": [],
            "panel": {
                "id": 3631,
                "hash_id": null,
                "name": "Growth failure",
                "disease_group": "",
                "disease_sub_group": "",
                "description": "This panel contains genes associated with growth failure in infancy/early childhood, either isolated or as part of another disorder.\r\n\r\nConsider applying this panel in individuals with:\r\n -Height Standard Deviation Score (SDS) <-3 (very significant short stature - well below the 0.4th centile)\r\nAND at least one of:\r\n- History of small for gestational age (birth weight and/or length <-2SDS)\r\n- Body disproportion, e.g. discrepancy between stature and head size\r\n- Dysmorphic features and congenital anomalies\r\n- Abnormalities in the GH-IGF axis (evidence of GH insensitivity or deficiency) and/or other pituitary hormonal deficiencies\r\n- Family history of significant short stature (1st and 2nd degree relatives) and/or consanguinity\r\n\r\nPrior to genomic testing consider:\r\n-Chromosomal microarray analysis (e.g. Turner syndrome)\r\n-Methylation analysis for Russell-Silver syndrome and Temple syndrome\r\n-Skeletal survey\r\n\r\nAcquired causes of short stature are relatively common.\r\n\r\nDepending on the specific clinical features present, consider applying the Skeletal dysplasia, Intellectual Disability, and/or Pituitary Hormone deficiency panels.\r\n\r\nWith thanks to Genomics England for the original design of this panel.",
                "status": "public",
                "version": "1.102",
                "version_created": "2026-04-01T10:17:12.005431+11:00",
                "relevant_disorders": [
                    "Failure to thrive",
                    "HP:0001508; Growth delay",
                    "HP:0001510"
                ],
                "stats": {
                    "number_of_genes": 204,
                    "number_of_strs": 0,
                    "number_of_regions": 4
                },
                "types": [
                    {
                        "name": "Victorian Clinical Genetics Services",
                        "slug": "victorian-clinical-genetics-services",
                        "description": "Panel used by VCGS."
                    },
                    {
                        "name": "Genetic Health Queensland",
                        "slug": "genetic-health-queensland",
                        "description": "Panel used by GHQ."
                    },
                    {
                        "name": "Royal Melbourne Hospital",
                        "slug": "royal-melbourne-hospital",
                        "description": "Royal Melbourne Hospital"
                    },
                    {
                        "name": "Rare Disease",
                        "slug": "rare-disease",
                        "description": "Rare disease panels"
                    }
                ],
                "child_panel_ids": []
            },
            "transcript": null
        },
        {
            "gene_data": {
                "alias": [
                    "DKFZP727C091",
                    "MSL1v1",
                    "CENP-36",
                    "NSL1"
                ],
                "biotype": "protein_coding",
                "hgnc_id": "HGNC:24565",
                "gene_name": "KAT8 regulatory NSL complex subunit 1",
                "omim_gene": [
                    "612452"
                ],
                "alias_name": [
                    "centromere protein 36"
                ],
                "gene_symbol": "KANSL1",
                "hgnc_symbol": "KANSL1",
                "hgnc_release": "2017-11-03",
                "ensembl_genes": {
                    "GRch37": {
                        "82": {
                            "location": "17:44107282-44302733",
                            "ensembl_id": "ENSG00000120071"
                        }
                    },
                    "GRch38": {
                        "90": {
                            "location": "17:46029916-46225389",
                            "ensembl_id": "ENSG00000120071"
                        }
                    }
                },
                "hgnc_date_symbol_changed": "2012-02-20"
            },
            "entity_type": "gene",
            "entity_name": "KANSL1",
            "confidence_level": "3",
            "penetrance": null,
            "mode_of_pathogenicity": null,
            "publications": [
                "22544363"
            ],
            "evidence": [
                "Expert Review Green",
                "Expert Review"
            ],
            "phenotypes": [
                "Koolen-De Vries syndrome (MIM#610443)"
            ],
            "mode_of_inheritance": "MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted",
            "tags": [
                "SV/CNV"
            ],
            "panel": {
                "id": 3631,
                "hash_id": null,
                "name": "Growth failure",
                "disease_group": "",
                "disease_sub_group": "",
                "description": "This panel contains genes associated with growth failure in infancy/early childhood, either isolated or as part of another disorder.\r\n\r\nConsider applying this panel in individuals with:\r\n -Height Standard Deviation Score (SDS) <-3 (very significant short stature - well below the 0.4th centile)\r\nAND at least one of:\r\n- History of small for gestational age (birth weight and/or length <-2SDS)\r\n- Body disproportion, e.g. discrepancy between stature and head size\r\n- Dysmorphic features and congenital anomalies\r\n- Abnormalities in the GH-IGF axis (evidence of GH insensitivity or deficiency) and/or other pituitary hormonal deficiencies\r\n- Family history of significant short stature (1st and 2nd degree relatives) and/or consanguinity\r\n\r\nPrior to genomic testing consider:\r\n-Chromosomal microarray analysis (e.g. Turner syndrome)\r\n-Methylation analysis for Russell-Silver syndrome and Temple syndrome\r\n-Skeletal survey\r\n\r\nAcquired causes of short stature are relatively common.\r\n\r\nDepending on the specific clinical features present, consider applying the Skeletal dysplasia, Intellectual Disability, and/or Pituitary Hormone deficiency panels.\r\n\r\nWith thanks to Genomics England for the original design of this panel.",
                "status": "public",
                "version": "1.102",
                "version_created": "2026-04-01T10:17:12.005431+11:00",
                "relevant_disorders": [
                    "Failure to thrive",
                    "HP:0001508; Growth delay",
                    "HP:0001510"
                ],
                "stats": {
                    "number_of_genes": 204,
                    "number_of_strs": 0,
                    "number_of_regions": 4
                },
                "types": [
                    {
                        "name": "Victorian Clinical Genetics Services",
                        "slug": "victorian-clinical-genetics-services",
                        "description": "Panel used by VCGS."
                    },
                    {
                        "name": "Genetic Health Queensland",
                        "slug": "genetic-health-queensland",
                        "description": "Panel used by GHQ."
                    },
                    {
                        "name": "Royal Melbourne Hospital",
                        "slug": "royal-melbourne-hospital",
                        "description": "Royal Melbourne Hospital"
                    },
                    {
                        "name": "Rare Disease",
                        "slug": "rare-disease",
                        "description": "Rare disease panels"
                    }
                ],
                "child_panel_ids": []
            },
            "transcript": []
        },
        {
            "gene_data": {
                "alias": [
                    "FAF"
                ],
                "biotype": "protein_coding",
                "hgnc_id": "HGNC:3587",
                "gene_name": "Fanconi anemia complementation group F",
                "omim_gene": [
                    "613897"
                ],
                "alias_name": null,
                "gene_symbol": "FANCF",
                "hgnc_symbol": "FANCF",
                "hgnc_release": "2017-11-03",
                "ensembl_genes": {
                    "GRch37": {
                        "82": {
                            "location": "11:22644079-22647387",
                            "ensembl_id": "ENSG00000183161"
                        }
                    },
                    "GRch38": {
                        "90": {
                            "location": "11:22622519-22626787",
                            "ensembl_id": "ENSG00000183161"
                        }
                    }
                },
                "hgnc_date_symbol_changed": "1998-08-26"
            },
            "entity_type": "gene",
            "entity_name": "FANCF",
            "confidence_level": "3",
            "penetrance": null,
            "mode_of_pathogenicity": "",
            "publications": [
                "10615118",
                "31288759"
            ],
            "evidence": [
                "Expert Review Green",
                "Genomics England PanelApp",
                "Victorian Clinical Genetics Services"
            ],
            "phenotypes": [
                "Fanconi anaemia, complementation group F 603467",
                "MONDO:0011325"
            ],
            "mode_of_inheritance": "BIALLELIC, autosomal or pseudoautosomal",
            "tags": [],
            "panel": {
                "id": 3631,
                "hash_id": null,
                "name": "Growth failure",
                "disease_group": "",
                "disease_sub_group": "",
                "description": "This panel contains genes associated with growth failure in infancy/early childhood, either isolated or as part of another disorder.\r\n\r\nConsider applying this panel in individuals with:\r\n -Height Standard Deviation Score (SDS) <-3 (very significant short stature - well below the 0.4th centile)\r\nAND at least one of:\r\n- History of small for gestational age (birth weight and/or length <-2SDS)\r\n- Body disproportion, e.g. discrepancy between stature and head size\r\n- Dysmorphic features and congenital anomalies\r\n- Abnormalities in the GH-IGF axis (evidence of GH insensitivity or deficiency) and/or other pituitary hormonal deficiencies\r\n- Family history of significant short stature (1st and 2nd degree relatives) and/or consanguinity\r\n\r\nPrior to genomic testing consider:\r\n-Chromosomal microarray analysis (e.g. Turner syndrome)\r\n-Methylation analysis for Russell-Silver syndrome and Temple syndrome\r\n-Skeletal survey\r\n\r\nAcquired causes of short stature are relatively common.\r\n\r\nDepending on the specific clinical features present, consider applying the Skeletal dysplasia, Intellectual Disability, and/or Pituitary Hormone deficiency panels.\r\n\r\nWith thanks to Genomics England for the original design of this panel.",
                "status": "public",
                "version": "1.102",
                "version_created": "2026-04-01T10:17:12.005431+11:00",
                "relevant_disorders": [
                    "Failure to thrive",
                    "HP:0001508; Growth delay",
                    "HP:0001510"
                ],
                "stats": {
                    "number_of_genes": 204,
                    "number_of_strs": 0,
                    "number_of_regions": 4
                },
                "types": [
                    {
                        "name": "Victorian Clinical Genetics Services",
                        "slug": "victorian-clinical-genetics-services",
                        "description": "Panel used by VCGS."
                    },
                    {
                        "name": "Genetic Health Queensland",
                        "slug": "genetic-health-queensland",
                        "description": "Panel used by GHQ."
                    },
                    {
                        "name": "Royal Melbourne Hospital",
                        "slug": "royal-melbourne-hospital",
                        "description": "Royal Melbourne Hospital"
                    },
                    {
                        "name": "Rare Disease",
                        "slug": "rare-disease",
                        "description": "Rare disease panels"
                    }
                ],
                "child_panel_ids": []
            },
            "transcript": null
        },
        {
            "gene_data": {
                "alias": [
                    "KIAA0441",
                    "BIF1",
                    "PATZ2"
                ],
                "biotype": "protein_coding",
                "hgnc_id": "HGNC:21143",
                "gene_name": "zinc finger and BTB domain containing 24",
                "omim_gene": [
                    "614064"
                ],
                "alias_name": [
                    "POZ (BTB) and AT hook containing zinc finger 2"
                ],
                "gene_symbol": "ZBTB24",
                "hgnc_symbol": "ZBTB24",
                "hgnc_release": "2017-11-03",
                "ensembl_genes": {
                    "GRch37": {
                        "82": {
                            "location": "6:109783797-109804440",
                            "ensembl_id": "ENSG00000112365"
                        }
                    },
                    "GRch38": {
                        "90": {
                            "location": "6:109462594-109483237",
                            "ensembl_id": "ENSG00000112365"
                        }
                    }
                },
                "hgnc_date_symbol_changed": "2004-04-16"
            },
            "entity_type": "gene",
            "entity_name": "ZBTB24",
            "confidence_level": "3",
            "penetrance": null,
            "mode_of_pathogenicity": null,
            "publications": [
                "21596365",
                "21906047",
                "23486536"
            ],
            "evidence": [
                "Expert Review Green",
                "Expert Review"
            ],
            "phenotypes": [
                "Immunodeficiency-centromeric instability-facial anomalies syndrome 2, MIM#\t614069",
                "MONDO:0013553"
            ],
            "mode_of_inheritance": "BIALLELIC, autosomal or pseudoautosomal",
            "tags": [],
            "panel": {
                "id": 3631,
                "hash_id": null,
                "name": "Growth failure",
                "disease_group": "",
                "disease_sub_group": "",
                "description": "This panel contains genes associated with growth failure in infancy/early childhood, either isolated or as part of another disorder.\r\n\r\nConsider applying this panel in individuals with:\r\n -Height Standard Deviation Score (SDS) <-3 (very significant short stature - well below the 0.4th centile)\r\nAND at least one of:\r\n- History of small for gestational age (birth weight and/or length <-2SDS)\r\n- Body disproportion, e.g. discrepancy between stature and head size\r\n- Dysmorphic features and congenital anomalies\r\n- Abnormalities in the GH-IGF axis (evidence of GH insensitivity or deficiency) and/or other pituitary hormonal deficiencies\r\n- Family history of significant short stature (1st and 2nd degree relatives) and/or consanguinity\r\n\r\nPrior to genomic testing consider:\r\n-Chromosomal microarray analysis (e.g. Turner syndrome)\r\n-Methylation analysis for Russell-Silver syndrome and Temple syndrome\r\n-Skeletal survey\r\n\r\nAcquired causes of short stature are relatively common.\r\n\r\nDepending on the specific clinical features present, consider applying the Skeletal dysplasia, Intellectual Disability, and/or Pituitary Hormone deficiency panels.\r\n\r\nWith thanks to Genomics England for the original design of this panel.",
                "status": "public",
                "version": "1.102",
                "version_created": "2026-04-01T10:17:12.005431+11:00",
                "relevant_disorders": [
                    "Failure to thrive",
                    "HP:0001508; Growth delay",
                    "HP:0001510"
                ],
                "stats": {
                    "number_of_genes": 204,
                    "number_of_strs": 0,
                    "number_of_regions": 4
                },
                "types": [
                    {
                        "name": "Victorian Clinical Genetics Services",
                        "slug": "victorian-clinical-genetics-services",
                        "description": "Panel used by VCGS."
                    },
                    {
                        "name": "Genetic Health Queensland",
                        "slug": "genetic-health-queensland",
                        "description": "Panel used by GHQ."
                    },
                    {
                        "name": "Royal Melbourne Hospital",
                        "slug": "royal-melbourne-hospital",
                        "description": "Royal Melbourne Hospital"
                    },
                    {
                        "name": "Rare Disease",
                        "slug": "rare-disease",
                        "description": "Rare disease panels"
                    }
                ],
                "child_panel_ids": []
            },
            "transcript": []
        },
        {
            "gene_data": {
                "alias": [
                    "DKFZP547N043",
                    "Spartan",
                    "DVC1"
                ],
                "biotype": "protein_coding",
                "hgnc_id": "HGNC:25356",
                "gene_name": "SprT-like N-terminal domain",
                "omim_gene": [
                    "616086"
                ],
                "alias_name": [
                    "SprT-like domain at the N terminus",
                    "DNA damage-targeting VCP (p97) adaptor"
                ],
                "gene_symbol": "SPRTN",
                "hgnc_symbol": "SPRTN",
                "hgnc_release": "2017-11-03",
                "ensembl_genes": {
                    "GRch37": {
                        "82": {
                            "location": "1:231472850-231490769",
                            "ensembl_id": "ENSG00000010072"
                        }
                    },
                    "GRch38": {
                        "90": {
                            "location": "1:231337104-231355023",
                            "ensembl_id": "ENSG00000010072"
                        }
                    }
                },
                "hgnc_date_symbol_changed": "2012-06-18"
            },
            "entity_type": "gene",
            "entity_name": "SPRTN",
            "confidence_level": "3",
            "penetrance": null,
            "mode_of_pathogenicity": null,
            "publications": [
                "25261934"
            ],
            "evidence": [
                "Expert Review Green",
                "Expert Review"
            ],
            "phenotypes": [
                "Ruijs-Aalfs syndrome, MIM# 616200",
                "MONDO:0014527"
            ],
            "mode_of_inheritance": "BIALLELIC, autosomal or pseudoautosomal",
            "tags": [],
            "panel": {
                "id": 3631,
                "hash_id": null,
                "name": "Growth failure",
                "disease_group": "",
                "disease_sub_group": "",
                "description": "This panel contains genes associated with growth failure in infancy/early childhood, either isolated or as part of another disorder.\r\n\r\nConsider applying this panel in individuals with:\r\n -Height Standard Deviation Score (SDS) <-3 (very significant short stature - well below the 0.4th centile)\r\nAND at least one of:\r\n- History of small for gestational age (birth weight and/or length <-2SDS)\r\n- Body disproportion, e.g. discrepancy between stature and head size\r\n- Dysmorphic features and congenital anomalies\r\n- Abnormalities in the GH-IGF axis (evidence of GH insensitivity or deficiency) and/or other pituitary hormonal deficiencies\r\n- Family history of significant short stature (1st and 2nd degree relatives) and/or consanguinity\r\n\r\nPrior to genomic testing consider:\r\n-Chromosomal microarray analysis (e.g. Turner syndrome)\r\n-Methylation analysis for Russell-Silver syndrome and Temple syndrome\r\n-Skeletal survey\r\n\r\nAcquired causes of short stature are relatively common.\r\n\r\nDepending on the specific clinical features present, consider applying the Skeletal dysplasia, Intellectual Disability, and/or Pituitary Hormone deficiency panels.\r\n\r\nWith thanks to Genomics England for the original design of this panel.",
                "status": "public",
                "version": "1.102",
                "version_created": "2026-04-01T10:17:12.005431+11:00",
                "relevant_disorders": [
                    "Failure to thrive",
                    "HP:0001508; Growth delay",
                    "HP:0001510"
                ],
                "stats": {
                    "number_of_genes": 204,
                    "number_of_strs": 0,
                    "number_of_regions": 4
                },
                "types": [
                    {
                        "name": "Victorian Clinical Genetics Services",
                        "slug": "victorian-clinical-genetics-services",
                        "description": "Panel used by VCGS."
                    },
                    {
                        "name": "Genetic Health Queensland",
                        "slug": "genetic-health-queensland",
                        "description": "Panel used by GHQ."
                    },
                    {
                        "name": "Royal Melbourne Hospital",
                        "slug": "royal-melbourne-hospital",
                        "description": "Royal Melbourne Hospital"
                    },
                    {
                        "name": "Rare Disease",
                        "slug": "rare-disease",
                        "description": "Rare disease panels"
                    }
                ],
                "child_panel_ids": []
            },
            "transcript": []
        },
        {
            "gene_data": {
                "alias": [
                    "FLJ35794"
                ],
                "biotype": "protein_coding",
                "hgnc_id": "HGNC:26661",
                "gene_name": "ring finger protein 168",
                "omim_gene": [
                    "612688"
                ],
                "alias_name": null,
                "gene_symbol": "RNF168",
                "hgnc_symbol": "RNF168",
                "hgnc_release": "2017-11-03",
                "ensembl_genes": {
                    "GRch37": {
                        "82": {
                            "location": "3:196195654-196230639",
                            "ensembl_id": "ENSG00000163961"
                        }
                    },
                    "GRch38": {
                        "90": {
                            "location": "3:196468783-196503768",
                            "ensembl_id": "ENSG00000163961"
                        }
                    }
                },
                "hgnc_date_symbol_changed": "2005-01-25"
            },
            "entity_type": "gene",
            "entity_name": "RNF168",
            "confidence_level": "3",
            "penetrance": null,
            "mode_of_pathogenicity": null,
            "publications": [
                "19203578",
                "21394101",
                "29255463",
                "21552324"
            ],
            "evidence": [
                "Expert Review Green",
                "Expert Review"
            ],
            "phenotypes": [
                "RIDDLE syndrome MIM# 611943",
                "Radiosensitivity",
                "Immune Deficiency",
                "Dysmorphic Features",
                "Learning difficulties",
                "Low IgG or IgA",
                "Short stature",
                "mild defect of motor control to ataxia",
                "normal intelligence to learning difficulties",
                "mild facial dysmorphism to microcephaly"
            ],
            "mode_of_inheritance": "BIALLELIC, autosomal or pseudoautosomal",
            "tags": [],
            "panel": {
                "id": 3631,
                "hash_id": null,
                "name": "Growth failure",
                "disease_group": "",
                "disease_sub_group": "",
                "description": "This panel contains genes associated with growth failure in infancy/early childhood, either isolated or as part of another disorder.\r\n\r\nConsider applying this panel in individuals with:\r\n -Height Standard Deviation Score (SDS) <-3 (very significant short stature - well below the 0.4th centile)\r\nAND at least one of:\r\n- History of small for gestational age (birth weight and/or length <-2SDS)\r\n- Body disproportion, e.g. discrepancy between stature and head size\r\n- Dysmorphic features and congenital anomalies\r\n- Abnormalities in the GH-IGF axis (evidence of GH insensitivity or deficiency) and/or other pituitary hormonal deficiencies\r\n- Family history of significant short stature (1st and 2nd degree relatives) and/or consanguinity\r\n\r\nPrior to genomic testing consider:\r\n-Chromosomal microarray analysis (e.g. Turner syndrome)\r\n-Methylation analysis for Russell-Silver syndrome and Temple syndrome\r\n-Skeletal survey\r\n\r\nAcquired causes of short stature are relatively common.\r\n\r\nDepending on the specific clinical features present, consider applying the Skeletal dysplasia, Intellectual Disability, and/or Pituitary Hormone deficiency panels.\r\n\r\nWith thanks to Genomics England for the original design of this panel.",
                "status": "public",
                "version": "1.102",
                "version_created": "2026-04-01T10:17:12.005431+11:00",
                "relevant_disorders": [
                    "Failure to thrive",
                    "HP:0001508; Growth delay",
                    "HP:0001510"
                ],
                "stats": {
                    "number_of_genes": 204,
                    "number_of_strs": 0,
                    "number_of_regions": 4
                },
                "types": [
                    {
                        "name": "Victorian Clinical Genetics Services",
                        "slug": "victorian-clinical-genetics-services",
                        "description": "Panel used by VCGS."
                    },
                    {
                        "name": "Genetic Health Queensland",
                        "slug": "genetic-health-queensland",
                        "description": "Panel used by GHQ."
                    },
                    {
                        "name": "Royal Melbourne Hospital",
                        "slug": "royal-melbourne-hospital",
                        "description": "Royal Melbourne Hospital"
                    },
                    {
                        "name": "Rare Disease",
                        "slug": "rare-disease",
                        "description": "Rare disease panels"
                    }
                ],
                "child_panel_ids": []
            },
            "transcript": []
        },
        {
            "gene_data": {
                "alias": [
                    "RecQ4"
                ],
                "biotype": "protein_coding",
                "hgnc_id": "HGNC:9949",
                "gene_name": "RecQ like helicase 4",
                "omim_gene": [
                    "603780"
                ],
                "alias_name": null,
                "gene_symbol": "RECQL4",
                "hgnc_symbol": "RECQL4",
                "hgnc_release": "2017-11-03",
                "ensembl_genes": {
                    "GRch37": {
                        "82": {
                            "location": "8:145736667-145743229",
                            "ensembl_id": "ENSG00000160957"
                        }
                    },
                    "GRch38": {
                        "90": {
                            "location": "8:144511288-144517845",
                            "ensembl_id": "ENSG00000160957"
                        }
                    }
                },
                "hgnc_date_symbol_changed": "2014-03-07"
            },
            "entity_type": "gene",
            "entity_name": "RECQL4",
            "confidence_level": "3",
            "penetrance": null,
            "mode_of_pathogenicity": null,
            "publications": [
                "10319867",
                "12952869",
                "15964893"
            ],
            "evidence": [
                "Expert Review Green",
                "Expert Review"
            ],
            "phenotypes": [
                "Rothmund-Thomson syndrome, type 2, MIM# 268400",
                "RAPADILINO syndrome, MIM# 266280",
                "Baller-Gerold syndrome, MIM# 218600"
            ],
            "mode_of_inheritance": "BIALLELIC, autosomal or pseudoautosomal",
            "tags": [],
            "panel": {
                "id": 3631,
                "hash_id": null,
                "name": "Growth failure",
                "disease_group": "",
                "disease_sub_group": "",
                "description": "This panel contains genes associated with growth failure in infancy/early childhood, either isolated or as part of another disorder.\r\n\r\nConsider applying this panel in individuals with:\r\n -Height Standard Deviation Score (SDS) <-3 (very significant short stature - well below the 0.4th centile)\r\nAND at least one of:\r\n- History of small for gestational age (birth weight and/or length <-2SDS)\r\n- Body disproportion, e.g. discrepancy between stature and head size\r\n- Dysmorphic features and congenital anomalies\r\n- Abnormalities in the GH-IGF axis (evidence of GH insensitivity or deficiency) and/or other pituitary hormonal deficiencies\r\n- Family history of significant short stature (1st and 2nd degree relatives) and/or consanguinity\r\n\r\nPrior to genomic testing consider:\r\n-Chromosomal microarray analysis (e.g. Turner syndrome)\r\n-Methylation analysis for Russell-Silver syndrome and Temple syndrome\r\n-Skeletal survey\r\n\r\nAcquired causes of short stature are relatively common.\r\n\r\nDepending on the specific clinical features present, consider applying the Skeletal dysplasia, Intellectual Disability, and/or Pituitary Hormone deficiency panels.\r\n\r\nWith thanks to Genomics England for the original design of this panel.",
                "status": "public",
                "version": "1.102",
                "version_created": "2026-04-01T10:17:12.005431+11:00",
                "relevant_disorders": [
                    "Failure to thrive",
                    "HP:0001508; Growth delay",
                    "HP:0001510"
                ],
                "stats": {
                    "number_of_genes": 204,
                    "number_of_strs": 0,
                    "number_of_regions": 4
                },
                "types": [
                    {
                        "name": "Victorian Clinical Genetics Services",
                        "slug": "victorian-clinical-genetics-services",
                        "description": "Panel used by VCGS."
                    },
                    {
                        "name": "Genetic Health Queensland",
                        "slug": "genetic-health-queensland",
                        "description": "Panel used by GHQ."
                    },
                    {
                        "name": "Royal Melbourne Hospital",
                        "slug": "royal-melbourne-hospital",
                        "description": "Royal Melbourne Hospital"
                    },
                    {
                        "name": "Rare Disease",
                        "slug": "rare-disease",
                        "description": "Rare disease panels"
                    }
                ],
                "child_panel_ids": []
            },
            "transcript": []
        },
        {
            "gene_data": {
                "alias": [
                    "RAD51L2",
                    "FANCO"
                ],
                "biotype": "protein_coding",
                "hgnc_id": "HGNC:9820",
                "gene_name": "RAD51 paralog C",
                "omim_gene": [
                    "602774"
                ],
                "alias_name": null,
                "gene_symbol": "RAD51C",
                "hgnc_symbol": "RAD51C",
                "hgnc_release": "2017-11-03",
                "ensembl_genes": {
                    "GRch37": {
                        "82": {
                            "location": "17:56769934-56811703",
                            "ensembl_id": "ENSG00000108384"
                        }
                    },
                    "GRch38": {
                        "90": {
                            "location": "17:58692573-58735611",
                            "ensembl_id": "ENSG00000108384"
                        }
                    }
                },
                "hgnc_date_symbol_changed": "1998-02-26"
            },
            "entity_type": "gene",
            "entity_name": "RAD51C",
            "confidence_level": "3",
            "penetrance": null,
            "mode_of_pathogenicity": null,
            "publications": [
                "20400963",
                "29278735"
            ],
            "evidence": [
                "Expert Review Green",
                "Expert Review"
            ],
            "phenotypes": [
                "Fanconi anaemia, complementation group O, MIM# 613390"
            ],
            "mode_of_inheritance": "BIALLELIC, autosomal or pseudoautosomal",
            "tags": [],
            "panel": {
                "id": 3631,
                "hash_id": null,
                "name": "Growth failure",
                "disease_group": "",
                "disease_sub_group": "",
                "description": "This panel contains genes associated with growth failure in infancy/early childhood, either isolated or as part of another disorder.\r\n\r\nConsider applying this panel in individuals with:\r\n -Height Standard Deviation Score (SDS) <-3 (very significant short stature - well below the 0.4th centile)\r\nAND at least one of:\r\n- History of small for gestational age (birth weight and/or length <-2SDS)\r\n- Body disproportion, e.g. discrepancy between stature and head size\r\n- Dysmorphic features and congenital anomalies\r\n- Abnormalities in the GH-IGF axis (evidence of GH insensitivity or deficiency) and/or other pituitary hormonal deficiencies\r\n- Family history of significant short stature (1st and 2nd degree relatives) and/or consanguinity\r\n\r\nPrior to genomic testing consider:\r\n-Chromosomal microarray analysis (e.g. Turner syndrome)\r\n-Methylation analysis for Russell-Silver syndrome and Temple syndrome\r\n-Skeletal survey\r\n\r\nAcquired causes of short stature are relatively common.\r\n\r\nDepending on the specific clinical features present, consider applying the Skeletal dysplasia, Intellectual Disability, and/or Pituitary Hormone deficiency panels.\r\n\r\nWith thanks to Genomics England for the original design of this panel.",
                "status": "public",
                "version": "1.102",
                "version_created": "2026-04-01T10:17:12.005431+11:00",
                "relevant_disorders": [
                    "Failure to thrive",
                    "HP:0001508; Growth delay",
                    "HP:0001510"
                ],
                "stats": {
                    "number_of_genes": 204,
                    "number_of_strs": 0,
                    "number_of_regions": 4
                },
                "types": [
                    {
                        "name": "Victorian Clinical Genetics Services",
                        "slug": "victorian-clinical-genetics-services",
                        "description": "Panel used by VCGS."
                    },
                    {
                        "name": "Genetic Health Queensland",
                        "slug": "genetic-health-queensland",
                        "description": "Panel used by GHQ."
                    },
                    {
                        "name": "Royal Melbourne Hospital",
                        "slug": "royal-melbourne-hospital",
                        "description": "Royal Melbourne Hospital"
                    },
                    {
                        "name": "Rare Disease",
                        "slug": "rare-disease",
                        "description": "Rare disease panels"
                    }
                ],
                "child_panel_ids": []
            },
            "transcript": []
        },
        {
            "gene_data": {
                "alias": [
                    "FAE"
                ],
                "biotype": "protein_coding",
                "hgnc_id": "HGNC:3586",
                "gene_name": "Fanconi anemia complementation group E",
                "omim_gene": [
                    "613976"
                ],
                "alias_name": null,
                "gene_symbol": "FANCE",
                "hgnc_symbol": "FANCE",
                "hgnc_release": "2017-11-03",
                "ensembl_genes": {
                    "GRch37": {
                        "82": {
                            "location": "6:35420138-35434880",
                            "ensembl_id": "ENSG00000112039"
                        }
                    },
                    "GRch38": {
                        "90": {
                            "location": "6:35452361-35467103",
                            "ensembl_id": "ENSG00000112039"
                        }
                    }
                },
                "hgnc_date_symbol_changed": "1996-04-09"
            },
            "entity_type": "gene",
            "entity_name": "FANCE",
            "confidence_level": "3",
            "penetrance": null,
            "mode_of_pathogenicity": "",
            "publications": [
                "11001585",
                "31586946",
                "7662964",
                "9382107",
                "9147877",
                "10205272"
            ],
            "evidence": [
                "Expert Review Green",
                "Genomics England PanelApp",
                "Victorian Clinical Genetics Services"
            ],
            "phenotypes": [
                "Fanconi anaemia, complementation group E, MIM# 600901",
                "MONDO:0010953"
            ],
            "mode_of_inheritance": "BIALLELIC, autosomal or pseudoautosomal",
            "tags": [],
            "panel": {
                "id": 3631,
                "hash_id": null,
                "name": "Growth failure",
                "disease_group": "",
                "disease_sub_group": "",
                "description": "This panel contains genes associated with growth failure in infancy/early childhood, either isolated or as part of another disorder.\r\n\r\nConsider applying this panel in individuals with:\r\n -Height Standard Deviation Score (SDS) <-3 (very significant short stature - well below the 0.4th centile)\r\nAND at least one of:\r\n- History of small for gestational age (birth weight and/or length <-2SDS)\r\n- Body disproportion, e.g. discrepancy between stature and head size\r\n- Dysmorphic features and congenital anomalies\r\n- Abnormalities in the GH-IGF axis (evidence of GH insensitivity or deficiency) and/or other pituitary hormonal deficiencies\r\n- Family history of significant short stature (1st and 2nd degree relatives) and/or consanguinity\r\n\r\nPrior to genomic testing consider:\r\n-Chromosomal microarray analysis (e.g. Turner syndrome)\r\n-Methylation analysis for Russell-Silver syndrome and Temple syndrome\r\n-Skeletal survey\r\n\r\nAcquired causes of short stature are relatively common.\r\n\r\nDepending on the specific clinical features present, consider applying the Skeletal dysplasia, Intellectual Disability, and/or Pituitary Hormone deficiency panels.\r\n\r\nWith thanks to Genomics England for the original design of this panel.",
                "status": "public",
                "version": "1.102",
                "version_created": "2026-04-01T10:17:12.005431+11:00",
                "relevant_disorders": [
                    "Failure to thrive",
                    "HP:0001508; Growth delay",
                    "HP:0001510"
                ],
                "stats": {
                    "number_of_genes": 204,
                    "number_of_strs": 0,
                    "number_of_regions": 4
                },
                "types": [
                    {
                        "name": "Victorian Clinical Genetics Services",
                        "slug": "victorian-clinical-genetics-services",
                        "description": "Panel used by VCGS."
                    },
                    {
                        "name": "Genetic Health Queensland",
                        "slug": "genetic-health-queensland",
                        "description": "Panel used by GHQ."
                    },
                    {
                        "name": "Royal Melbourne Hospital",
                        "slug": "royal-melbourne-hospital",
                        "description": "Royal Melbourne Hospital"
                    },
                    {
                        "name": "Rare Disease",
                        "slug": "rare-disease",
                        "description": "Rare disease panels"
                    }
                ],
                "child_panel_ids": []
            },
            "transcript": null
        },
        {
            "gene_data": {
                "alias": [
                    "HsRad51",
                    "HsT16930",
                    "BRCC5",
                    "FANCR"
                ],
                "biotype": "protein_coding",
                "hgnc_id": "HGNC:9817",
                "gene_name": "RAD51 recombinase",
                "omim_gene": [
                    "179617"
                ],
                "alias_name": [
                    "BRCA1/BRCA2-containing complex, subunit 5"
                ],
                "gene_symbol": "RAD51",
                "hgnc_symbol": "RAD51",
                "hgnc_release": "2017-11-03",
                "ensembl_genes": {
                    "GRch37": {
                        "82": {
                            "location": "15:40986972-41024354",
                            "ensembl_id": "ENSG00000051180"
                        }
                    },
                    "GRch38": {
                        "90": {
                            "location": "15:40694774-40732339",
                            "ensembl_id": "ENSG00000051180"
                        }
                    }
                },
                "hgnc_date_symbol_changed": "1993-05-26"
            },
            "entity_type": "gene",
            "entity_name": "RAD51",
            "confidence_level": "3",
            "penetrance": null,
            "mode_of_pathogenicity": null,
            "publications": [
                "26253028",
                "26681308",
                "30907510"
            ],
            "evidence": [
                "Expert Review Green",
                "Expert Review"
            ],
            "phenotypes": [
                "Fanconi anaemia, complementation group R, MIM# 617244"
            ],
            "mode_of_inheritance": "MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted",
            "tags": [],
            "panel": {
                "id": 3631,
                "hash_id": null,
                "name": "Growth failure",
                "disease_group": "",
                "disease_sub_group": "",
                "description": "This panel contains genes associated with growth failure in infancy/early childhood, either isolated or as part of another disorder.\r\n\r\nConsider applying this panel in individuals with:\r\n -Height Standard Deviation Score (SDS) <-3 (very significant short stature - well below the 0.4th centile)\r\nAND at least one of:\r\n- History of small for gestational age (birth weight and/or length <-2SDS)\r\n- Body disproportion, e.g. discrepancy between stature and head size\r\n- Dysmorphic features and congenital anomalies\r\n- Abnormalities in the GH-IGF axis (evidence of GH insensitivity or deficiency) and/or other pituitary hormonal deficiencies\r\n- Family history of significant short stature (1st and 2nd degree relatives) and/or consanguinity\r\n\r\nPrior to genomic testing consider:\r\n-Chromosomal microarray analysis (e.g. Turner syndrome)\r\n-Methylation analysis for Russell-Silver syndrome and Temple syndrome\r\n-Skeletal survey\r\n\r\nAcquired causes of short stature are relatively common.\r\n\r\nDepending on the specific clinical features present, consider applying the Skeletal dysplasia, Intellectual Disability, and/or Pituitary Hormone deficiency panels.\r\n\r\nWith thanks to Genomics England for the original design of this panel.",
                "status": "public",
                "version": "1.102",
                "version_created": "2026-04-01T10:17:12.005431+11:00",
                "relevant_disorders": [
                    "Failure to thrive",
                    "HP:0001508; Growth delay",
                    "HP:0001510"
                ],
                "stats": {
                    "number_of_genes": 204,
                    "number_of_strs": 0,
                    "number_of_regions": 4
                },
                "types": [
                    {
                        "name": "Victorian Clinical Genetics Services",
                        "slug": "victorian-clinical-genetics-services",
                        "description": "Panel used by VCGS."
                    },
                    {
                        "name": "Genetic Health Queensland",
                        "slug": "genetic-health-queensland",
                        "description": "Panel used by GHQ."
                    },
                    {
                        "name": "Royal Melbourne Hospital",
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                        "description": "Royal Melbourne Hospital"
                    },
                    {
                        "name": "Rare Disease",
                        "slug": "rare-disease",
                        "description": "Rare disease panels"
                    }
                ],
                "child_panel_ids": []
            },
            "transcript": []
        },
        {
            "gene_data": {
                "alias": [
                    "hRad50",
                    "RAD50-2"
                ],
                "biotype": "protein_coding",
                "hgnc_id": "HGNC:9816",
                "gene_name": "RAD50 double strand break repair protein",
                "omim_gene": [
                    "604040"
                ],
                "alias_name": null,
                "gene_symbol": "RAD50",
                "hgnc_symbol": "RAD50",
                "hgnc_release": "2017-11-03",
                "ensembl_genes": {
                    "GRch37": {
                        "82": {
                            "location": "5:131891711-131980313",
                            "ensembl_id": "ENSG00000113522"
                        }
                    },
                    "GRch38": {
                        "90": {
                            "location": "5:132556019-132646344",
                            "ensembl_id": "ENSG00000113522"
                        }
                    }
                },
                "hgnc_date_symbol_changed": "1999-07-23"
            },
            "entity_type": "gene",
            "entity_name": "RAD50",
            "confidence_level": "3",
            "penetrance": null,
            "mode_of_pathogenicity": null,
            "publications": [
                "19409520",
                "32212377",
                "33378670"
            ],
            "evidence": [
                "Expert Review Green",
                "Expert Review"
            ],
            "phenotypes": [
                "Nijmegen breakage syndrome-like disorder, MIM# 613078",
                "MONDO:0013118"
            ],
            "mode_of_inheritance": "BIALLELIC, autosomal or pseudoautosomal",
            "tags": [],
            "panel": {
                "id": 3631,
                "hash_id": null,
                "name": "Growth failure",
                "disease_group": "",
                "disease_sub_group": "",
                "description": "This panel contains genes associated with growth failure in infancy/early childhood, either isolated or as part of another disorder.\r\n\r\nConsider applying this panel in individuals with:\r\n -Height Standard Deviation Score (SDS) <-3 (very significant short stature - well below the 0.4th centile)\r\nAND at least one of:\r\n- History of small for gestational age (birth weight and/or length <-2SDS)\r\n- Body disproportion, e.g. discrepancy between stature and head size\r\n- Dysmorphic features and congenital anomalies\r\n- Abnormalities in the GH-IGF axis (evidence of GH insensitivity or deficiency) and/or other pituitary hormonal deficiencies\r\n- Family history of significant short stature (1st and 2nd degree relatives) and/or consanguinity\r\n\r\nPrior to genomic testing consider:\r\n-Chromosomal microarray analysis (e.g. Turner syndrome)\r\n-Methylation analysis for Russell-Silver syndrome and Temple syndrome\r\n-Skeletal survey\r\n\r\nAcquired causes of short stature are relatively common.\r\n\r\nDepending on the specific clinical features present, consider applying the Skeletal dysplasia, Intellectual Disability, and/or Pituitary Hormone deficiency panels.\r\n\r\nWith thanks to Genomics England for the original design of this panel.",
                "status": "public",
                "version": "1.102",
                "version_created": "2026-04-01T10:17:12.005431+11:00",
                "relevant_disorders": [
                    "Failure to thrive",
                    "HP:0001508; Growth delay",
                    "HP:0001510"
                ],
                "stats": {
                    "number_of_genes": 204,
                    "number_of_strs": 0,
                    "number_of_regions": 4
                },
                "types": [
                    {
                        "name": "Victorian Clinical Genetics Services",
                        "slug": "victorian-clinical-genetics-services",
                        "description": "Panel used by VCGS."
                    },
                    {
                        "name": "Genetic Health Queensland",
                        "slug": "genetic-health-queensland",
                        "description": "Panel used by GHQ."
                    },
                    {
                        "name": "Royal Melbourne Hospital",
                        "slug": "royal-melbourne-hospital",
                        "description": "Royal Melbourne Hospital"
                    },
                    {
                        "name": "Rare Disease",
                        "slug": "rare-disease",
                        "description": "Rare disease panels"
                    }
                ],
                "child_panel_ids": []
            },
            "transcript": []
        },
        {
            "gene_data": {
                "alias": [
                    "Cernunnos",
                    "XLF",
                    "FLJ12610"
                ],
                "biotype": "protein_coding",
                "hgnc_id": "HGNC:25737",
                "gene_name": "non-homologous end joining factor 1",
                "omim_gene": [
                    "611290"
                ],
                "alias_name": [
                    "XRCC4-like factor"
                ],
                "gene_symbol": "NHEJ1",
                "hgnc_symbol": "NHEJ1",
                "hgnc_release": "2017-11-03",
                "ensembl_genes": {
                    "GRch37": {
                        "82": {
                            "location": "2:219940039-220025587",
                            "ensembl_id": "ENSG00000187736"
                        }
                    },
                    "GRch38": {
                        "90": {
                            "location": "2:219075317-219160865",
                            "ensembl_id": "ENSG00000187736"
                        }
                    }
                },
                "hgnc_date_symbol_changed": "2006-03-30"
            },
            "entity_type": "gene",
            "entity_name": "NHEJ1",
            "confidence_level": "3",
            "penetrance": null,
            "mode_of_pathogenicity": null,
            "publications": [
                "16439204",
                "16439205"
            ],
            "evidence": [
                "Expert Review Green",
                "Expert Review"
            ],
            "phenotypes": [
                "Severe combined immunodeficiency with microcephaly, growth retardation, and sensitivity to ionizing radiation, MIM# 611291",
                "MONDO:0012650"
            ],
            "mode_of_inheritance": "BIALLELIC, autosomal or pseudoautosomal",
            "tags": [],
            "panel": {
                "id": 3631,
                "hash_id": null,
                "name": "Growth failure",
                "disease_group": "",
                "disease_sub_group": "",
                "description": "This panel contains genes associated with growth failure in infancy/early childhood, either isolated or as part of another disorder.\r\n\r\nConsider applying this panel in individuals with:\r\n -Height Standard Deviation Score (SDS) <-3 (very significant short stature - well below the 0.4th centile)\r\nAND at least one of:\r\n- History of small for gestational age (birth weight and/or length <-2SDS)\r\n- Body disproportion, e.g. discrepancy between stature and head size\r\n- Dysmorphic features and congenital anomalies\r\n- Abnormalities in the GH-IGF axis (evidence of GH insensitivity or deficiency) and/or other pituitary hormonal deficiencies\r\n- Family history of significant short stature (1st and 2nd degree relatives) and/or consanguinity\r\n\r\nPrior to genomic testing consider:\r\n-Chromosomal microarray analysis (e.g. Turner syndrome)\r\n-Methylation analysis for Russell-Silver syndrome and Temple syndrome\r\n-Skeletal survey\r\n\r\nAcquired causes of short stature are relatively common.\r\n\r\nDepending on the specific clinical features present, consider applying the Skeletal dysplasia, Intellectual Disability, and/or Pituitary Hormone deficiency panels.\r\n\r\nWith thanks to Genomics England for the original design of this panel.",
                "status": "public",
                "version": "1.102",
                "version_created": "2026-04-01T10:17:12.005431+11:00",
                "relevant_disorders": [
                    "Failure to thrive",
                    "HP:0001508; Growth delay",
                    "HP:0001510"
                ],
                "stats": {
                    "number_of_genes": 204,
                    "number_of_strs": 0,
                    "number_of_regions": 4
                },
                "types": [
                    {
                        "name": "Victorian Clinical Genetics Services",
                        "slug": "victorian-clinical-genetics-services",
                        "description": "Panel used by VCGS."
                    },
                    {
                        "name": "Genetic Health Queensland",
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                        "description": "Panel used by GHQ."
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                    {
                        "name": "Royal Melbourne Hospital",
                        "slug": "royal-melbourne-hospital",
                        "description": "Royal Melbourne Hospital"
                    },
                    {
                        "name": "Rare Disease",
                        "slug": "rare-disease",
                        "description": "Rare disease panels"
                    }
                ],
                "child_panel_ids": []
            },
            "transcript": []
        },
        {
            "gene_data": {
                "alias": [
                    "FAD",
                    "FA-D2"
                ],
                "biotype": "protein_coding",
                "hgnc_id": "HGNC:3585",
                "gene_name": "Fanconi anemia complementation group D2",
                "omim_gene": [
                    "613984"
                ],
                "alias_name": null,
                "gene_symbol": "FANCD2",
                "hgnc_symbol": "FANCD2",
                "hgnc_release": "2017-11-03",
                "ensembl_genes": {
                    "GRch37": {
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                            "location": "3:10068098-10143614",
                            "ensembl_id": "ENSG00000144554"
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                    },
                    "GRch38": {
                        "90": {
                            "location": "3:10026414-10101930",
                            "ensembl_id": "ENSG00000144554"
                        }
                    }
                },
                "hgnc_date_symbol_changed": "2001-10-05"
            },
            "entity_type": "gene",
            "entity_name": "FANCD2",
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            "penetrance": null,
            "mode_of_pathogenicity": "",
            "publications": [
                "11239454"
            ],
            "evidence": [
                "Expert Review Green",
                "Genomics England PanelApp",
                "Victorian Clinical Genetics Services"
            ],
            "phenotypes": [
                "Fanconi anaemia, complementation group D2, MIM# 227646"
            ],
            "mode_of_inheritance": "BIALLELIC, autosomal or pseudoautosomal",
            "tags": [],
            "panel": {
                "id": 3631,
                "hash_id": null,
                "name": "Growth failure",
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                "description": "This panel contains genes associated with growth failure in infancy/early childhood, either isolated or as part of another disorder.\r\n\r\nConsider applying this panel in individuals with:\r\n -Height Standard Deviation Score (SDS) <-3 (very significant short stature - well below the 0.4th centile)\r\nAND at least one of:\r\n- History of small for gestational age (birth weight and/or length <-2SDS)\r\n- Body disproportion, e.g. discrepancy between stature and head size\r\n- Dysmorphic features and congenital anomalies\r\n- Abnormalities in the GH-IGF axis (evidence of GH insensitivity or deficiency) and/or other pituitary hormonal deficiencies\r\n- Family history of significant short stature (1st and 2nd degree relatives) and/or consanguinity\r\n\r\nPrior to genomic testing consider:\r\n-Chromosomal microarray analysis (e.g. Turner syndrome)\r\n-Methylation analysis for Russell-Silver syndrome and Temple syndrome\r\n-Skeletal survey\r\n\r\nAcquired causes of short stature are relatively common.\r\n\r\nDepending on the specific clinical features present, consider applying the Skeletal dysplasia, Intellectual Disability, and/or Pituitary Hormone deficiency panels.\r\n\r\nWith thanks to Genomics England for the original design of this panel.",
                "status": "public",
                "version": "1.102",
                "version_created": "2026-04-01T10:17:12.005431+11:00",
                "relevant_disorders": [
                    "Failure to thrive",
                    "HP:0001508; Growth delay",
                    "HP:0001510"
                ],
                "stats": {
                    "number_of_genes": 204,
                    "number_of_strs": 0,
                    "number_of_regions": 4
                },
                "types": [
                    {
                        "name": "Victorian Clinical Genetics Services",
                        "slug": "victorian-clinical-genetics-services",
                        "description": "Panel used by VCGS."
                    },
                    {
                        "name": "Genetic Health Queensland",
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                        "description": "Panel used by GHQ."
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                    {
                        "name": "Royal Melbourne Hospital",
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                        "description": "Royal Melbourne Hospital"
                    },
                    {
                        "name": "Rare Disease",
                        "slug": "rare-disease",
                        "description": "Rare disease panels"
                    }
                ],
                "child_panel_ids": []
            },
            "transcript": null
        },
        {
            "gene_data": {
                "alias": [
                    "ORF20",
                    "TTDN1"
                ],
                "biotype": "protein_coding",
                "hgnc_id": "HGNC:16002",
                "gene_name": "M-phase specific PLK1 interacting protein",
                "omim_gene": [
                    "609188"
                ],
                "alias_name": null,
                "gene_symbol": "MPLKIP",
                "hgnc_symbol": "MPLKIP",
                "hgnc_release": "2017-11-03",
                "ensembl_genes": {
                    "GRch37": {
                        "82": {
                            "location": "7:40165622-40174258",
                            "ensembl_id": "ENSG00000168303"
                        }
                    },
                    "GRch38": {
                        "90": {
                            "location": "7:40126023-40134659",
                            "ensembl_id": "ENSG00000168303"
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                    }
                },
                "hgnc_date_symbol_changed": "2012-03-01"
            },
            "entity_type": "gene",
            "entity_name": "MPLKIP",
            "confidence_level": "3",
            "penetrance": null,
            "mode_of_pathogenicity": null,
            "publications": [
                "15645389",
                "16977596"
            ],
            "evidence": [
                "Expert Review Green",
                "Expert list"
            ],
            "phenotypes": [
                "Trichothiodystrophy 4, nonphotosensitive, MIM# 234050",
                "MONDO:0021013"
            ],
            "mode_of_inheritance": "BIALLELIC, autosomal or pseudoautosomal",
            "tags": [],
            "panel": {
                "id": 3631,
                "hash_id": null,
                "name": "Growth failure",
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                "description": "This panel contains genes associated with growth failure in infancy/early childhood, either isolated or as part of another disorder.\r\n\r\nConsider applying this panel in individuals with:\r\n -Height Standard Deviation Score (SDS) <-3 (very significant short stature - well below the 0.4th centile)\r\nAND at least one of:\r\n- History of small for gestational age (birth weight and/or length <-2SDS)\r\n- Body disproportion, e.g. discrepancy between stature and head size\r\n- Dysmorphic features and congenital anomalies\r\n- Abnormalities in the GH-IGF axis (evidence of GH insensitivity or deficiency) and/or other pituitary hormonal deficiencies\r\n- Family history of significant short stature (1st and 2nd degree relatives) and/or consanguinity\r\n\r\nPrior to genomic testing consider:\r\n-Chromosomal microarray analysis (e.g. Turner syndrome)\r\n-Methylation analysis for Russell-Silver syndrome and Temple syndrome\r\n-Skeletal survey\r\n\r\nAcquired causes of short stature are relatively common.\r\n\r\nDepending on the specific clinical features present, consider applying the Skeletal dysplasia, Intellectual Disability, and/or Pituitary Hormone deficiency panels.\r\n\r\nWith thanks to Genomics England for the original design of this panel.",
                "status": "public",
                "version": "1.102",
                "version_created": "2026-04-01T10:17:12.005431+11:00",
                "relevant_disorders": [
                    "Failure to thrive",
                    "HP:0001508; Growth delay",
                    "HP:0001510"
                ],
                "stats": {
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                    "number_of_strs": 0,
                    "number_of_regions": 4
                },
                "types": [
                    {
                        "name": "Victorian Clinical Genetics Services",
                        "slug": "victorian-clinical-genetics-services",
                        "description": "Panel used by VCGS."
                    },
                    {
                        "name": "Genetic Health Queensland",
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                        "description": "Panel used by GHQ."
                    },
                    {
                        "name": "Royal Melbourne Hospital",
                        "slug": "royal-melbourne-hospital",
                        "description": "Royal Melbourne Hospital"
                    },
                    {
                        "name": "Rare Disease",
                        "slug": "rare-disease",
                        "description": "Rare disease panels"
                    }
                ],
                "child_panel_ids": []
            },
            "transcript": []
        },
        {
            "gene_data": {
                "alias": [
                    "FLJ30544",
                    "bA120J8.2",
                    "TTD-A",
                    "TFB5",
                    "TFIIH",
                    "TTDA"
                ],
                "biotype": "protein_coding",
                "hgnc_id": "HGNC:21157",
                "gene_name": "general transcription factor IIH subunit 5",
                "omim_gene": [
                    "608780"
                ],
                "alias_name": [
                    "DNA repair syndrome trichothiodystrophy group A"
                ],
                "gene_symbol": "GTF2H5",
                "hgnc_symbol": "GTF2H5",
                "hgnc_release": "2017-11-03",
                "ensembl_genes": {
                    "GRch37": {
                        "82": {
                            "location": "6:158589384-158620376",
                            "ensembl_id": "ENSG00000272047"
                        }
                    },
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                            "location": "6:158168352-158199344",
                            "ensembl_id": "ENSG00000272047"
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                    }
                },
                "hgnc_date_symbol_changed": "2004-07-16"
            },
            "entity_type": "gene",
            "entity_name": "GTF2H5",
            "confidence_level": "3",
            "penetrance": null,
            "mode_of_pathogenicity": null,
            "publications": [
                "15220921",
                "30359777",
                "24986372"
            ],
            "evidence": [
                "Expert Review Green",
                "Expert Review"
            ],
            "phenotypes": [
                "Trichothiodystrophy 3, photosensitive, MIM# 616395",
                "MONDO:0014619"
            ],
            "mode_of_inheritance": "BIALLELIC, autosomal or pseudoautosomal",
            "tags": [],
            "panel": {
                "id": 3631,
                "hash_id": null,
                "name": "Growth failure",
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                "disease_sub_group": "",
                "description": "This panel contains genes associated with growth failure in infancy/early childhood, either isolated or as part of another disorder.\r\n\r\nConsider applying this panel in individuals with:\r\n -Height Standard Deviation Score (SDS) <-3 (very significant short stature - well below the 0.4th centile)\r\nAND at least one of:\r\n- History of small for gestational age (birth weight and/or length <-2SDS)\r\n- Body disproportion, e.g. discrepancy between stature and head size\r\n- Dysmorphic features and congenital anomalies\r\n- Abnormalities in the GH-IGF axis (evidence of GH insensitivity or deficiency) and/or other pituitary hormonal deficiencies\r\n- Family history of significant short stature (1st and 2nd degree relatives) and/or consanguinity\r\n\r\nPrior to genomic testing consider:\r\n-Chromosomal microarray analysis (e.g. Turner syndrome)\r\n-Methylation analysis for Russell-Silver syndrome and Temple syndrome\r\n-Skeletal survey\r\n\r\nAcquired causes of short stature are relatively common.\r\n\r\nDepending on the specific clinical features present, consider applying the Skeletal dysplasia, Intellectual Disability, and/or Pituitary Hormone deficiency panels.\r\n\r\nWith thanks to Genomics England for the original design of this panel.",
                "status": "public",
                "version": "1.102",
                "version_created": "2026-04-01T10:17:12.005431+11:00",
                "relevant_disorders": [
                    "Failure to thrive",
                    "HP:0001508; Growth delay",
                    "HP:0001510"
                ],
                "stats": {
                    "number_of_genes": 204,
                    "number_of_strs": 0,
                    "number_of_regions": 4
                },
                "types": [
                    {
                        "name": "Victorian Clinical Genetics Services",
                        "slug": "victorian-clinical-genetics-services",
                        "description": "Panel used by VCGS."
                    },
                    {
                        "name": "Genetic Health Queensland",
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                        "description": "Panel used by GHQ."
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                    {
                        "name": "Royal Melbourne Hospital",
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                        "description": "Royal Melbourne Hospital"
                    },
                    {
                        "name": "Rare Disease",
                        "slug": "rare-disease",
                        "description": "Rare disease panels"
                    }
                ],
                "child_panel_ids": []
            },
            "transcript": []
        },
        {
            "gene_data": {
                "alias": [],
                "biotype": "protein_coding",
                "hgnc_id": "HGNC:3437",
                "gene_name": "ERCC excision repair 5, endonuclease",
                "omim_gene": [
                    "133530"
                ],
                "alias_name": [
                    "Cockayne syndrome"
                ],
                "gene_symbol": "ERCC5",
                "hgnc_symbol": "ERCC5",
                "hgnc_release": "2017-11-03",
                "ensembl_genes": {
                    "GRch37": {
                        "82": {
                            "location": "13:103497194-103528345",
                            "ensembl_id": "ENSG00000134899"
                        }
                    },
                    "GRch38": {
                        "90": {
                            "location": "13:102844844-102876001",
                            "ensembl_id": "ENSG00000134899"
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                    }
                },
                "hgnc_date_symbol_changed": "2001-06-22"
            },
            "entity_type": "gene",
            "entity_name": "ERCC5",
            "confidence_level": "3",
            "penetrance": null,
            "mode_of_pathogenicity": null,
            "publications": [
                "7951246",
                "9096355",
                "9096355",
                "24700531",
                "33766032",
                "33219753"
            ],
            "evidence": [
                "Expert Review Green",
                "Expert Review"
            ],
            "phenotypes": [
                "Cerebrooculofacioskeletal syndrome 3, MIM# 616570",
                "MONDO:0014696",
                "Xeroderma pigmentosum, group G, MIM# 278780",
                "MONDO:0010216"
            ],
            "mode_of_inheritance": "BIALLELIC, autosomal or pseudoautosomal",
            "tags": [],
            "panel": {
                "id": 3631,
                "hash_id": null,
                "name": "Growth failure",
                "disease_group": "",
                "disease_sub_group": "",
                "description": "This panel contains genes associated with growth failure in infancy/early childhood, either isolated or as part of another disorder.\r\n\r\nConsider applying this panel in individuals with:\r\n -Height Standard Deviation Score (SDS) <-3 (very significant short stature - well below the 0.4th centile)\r\nAND at least one of:\r\n- History of small for gestational age (birth weight and/or length <-2SDS)\r\n- Body disproportion, e.g. discrepancy between stature and head size\r\n- Dysmorphic features and congenital anomalies\r\n- Abnormalities in the GH-IGF axis (evidence of GH insensitivity or deficiency) and/or other pituitary hormonal deficiencies\r\n- Family history of significant short stature (1st and 2nd degree relatives) and/or consanguinity\r\n\r\nPrior to genomic testing consider:\r\n-Chromosomal microarray analysis (e.g. Turner syndrome)\r\n-Methylation analysis for Russell-Silver syndrome and Temple syndrome\r\n-Skeletal survey\r\n\r\nAcquired causes of short stature are relatively common.\r\n\r\nDepending on the specific clinical features present, consider applying the Skeletal dysplasia, Intellectual Disability, and/or Pituitary Hormone deficiency panels.\r\n\r\nWith thanks to Genomics England for the original design of this panel.",
                "status": "public",
                "version": "1.102",
                "version_created": "2026-04-01T10:17:12.005431+11:00",
                "relevant_disorders": [
                    "Failure to thrive",
                    "HP:0001508; Growth delay",
                    "HP:0001510"
                ],
                "stats": {
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                    "number_of_strs": 0,
                    "number_of_regions": 4
                },
                "types": [
                    {
                        "name": "Victorian Clinical Genetics Services",
                        "slug": "victorian-clinical-genetics-services",
                        "description": "Panel used by VCGS."
                    },
                    {
                        "name": "Genetic Health Queensland",
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                    {
                        "name": "Royal Melbourne Hospital",
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                        "description": "Royal Melbourne Hospital"
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                        "name": "Rare Disease",
                        "slug": "rare-disease",
                        "description": "Rare disease panels"
                    }
                ],
                "child_panel_ids": []
            },
            "transcript": []
        },
        {
            "gene_data": {
                "alias": [
                    "XPB",
                    "BTF2",
                    "RAD25",
                    "TFIIH",
                    "GTF2H"
                ],
                "biotype": "protein_coding",
                "hgnc_id": "HGNC:3435",
                "gene_name": "ERCC excision repair 3, TFIIH core complex helicase subunit",
                "omim_gene": [
                    "133510"
                ],
                "alias_name": [
                    "xeroderma pigmentosum group B complementing"
                ],
                "gene_symbol": "ERCC3",
                "hgnc_symbol": "ERCC3",
                "hgnc_release": "2017-11-03",
                "ensembl_genes": {
                    "GRch37": {
                        "82": {
                            "location": "2:128014866-128051752",
                            "ensembl_id": "ENSG00000163161"
                        }
                    },
                    "GRch38": {
                        "90": {
                            "location": "2:127257290-127294176",
                            "ensembl_id": "ENSG00000163161"
                        }
                    }
                },
                "hgnc_date_symbol_changed": "2001-06-22"
            },
            "entity_type": "gene",
            "entity_name": "ERCC3",
            "confidence_level": "3",
            "penetrance": null,
            "mode_of_pathogenicity": null,
            "publications": [
                "2167179",
                "10447254",
                "16947863",
                "9012405",
                "32557569",
                "27004399"
            ],
            "evidence": [
                "Expert Review Green",
                "Expert Review"
            ],
            "phenotypes": [
                "Trichothiodystrophy 2, photosensitive, MIM# 616390",
                "Xeroderma pigmentosum, group B 61, MIM#0651"
            ],
            "mode_of_inheritance": "BIALLELIC, autosomal or pseudoautosomal",
            "tags": [],
            "panel": {
                "id": 3631,
                "hash_id": null,
                "name": "Growth failure",
                "disease_group": "",
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                "description": "This panel contains genes associated with growth failure in infancy/early childhood, either isolated or as part of another disorder.\r\n\r\nConsider applying this panel in individuals with:\r\n -Height Standard Deviation Score (SDS) <-3 (very significant short stature - well below the 0.4th centile)\r\nAND at least one of:\r\n- History of small for gestational age (birth weight and/or length <-2SDS)\r\n- Body disproportion, e.g. discrepancy between stature and head size\r\n- Dysmorphic features and congenital anomalies\r\n- Abnormalities in the GH-IGF axis (evidence of GH insensitivity or deficiency) and/or other pituitary hormonal deficiencies\r\n- Family history of significant short stature (1st and 2nd degree relatives) and/or consanguinity\r\n\r\nPrior to genomic testing consider:\r\n-Chromosomal microarray analysis (e.g. Turner syndrome)\r\n-Methylation analysis for Russell-Silver syndrome and Temple syndrome\r\n-Skeletal survey\r\n\r\nAcquired causes of short stature are relatively common.\r\n\r\nDepending on the specific clinical features present, consider applying the Skeletal dysplasia, Intellectual Disability, and/or Pituitary Hormone deficiency panels.\r\n\r\nWith thanks to Genomics England for the original design of this panel.",
                "status": "public",
                "version": "1.102",
                "version_created": "2026-04-01T10:17:12.005431+11:00",
                "relevant_disorders": [
                    "Failure to thrive",
                    "HP:0001508; Growth delay",
                    "HP:0001510"
                ],
                "stats": {
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                    "number_of_strs": 0,
                    "number_of_regions": 4
                },
                "types": [
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                        "name": "Victorian Clinical Genetics Services",
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                    },
                    {
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                    },
                    {
                        "name": "Royal Melbourne Hospital",
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                    },
                    {
                        "name": "Rare Disease",
                        "slug": "rare-disease",
                        "description": "Rare disease panels"
                    }
                ],
                "child_panel_ids": []
            },
            "transcript": []
        },
        {
            "gene_data": {
                "alias": [
                    "MAG",
                    "EM9",
                    "MGC102762",
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                    "MGC126219",
                    "TFIIH"
                ],
                "biotype": "protein_coding",
                "hgnc_id": "HGNC:3434",
                "gene_name": "ERCC excision repair 2, TFIIH core complex helicase subunit",
                "omim_gene": [
                    "126340"
                ],
                "alias_name": [
                    "excision repair cross-complementing rodent repair deficiency, complementation group 2 protein",
                    "TFIIH basal transcription factor complex helicase XPB subunit"
                ],
                "gene_symbol": "ERCC2",
                "hgnc_symbol": "ERCC2",
                "hgnc_release": "2017-11-03",
                "ensembl_genes": {
                    "GRch37": {
                        "82": {
                            "location": "19:45853095-45874176",
                            "ensembl_id": "ENSG00000104884"
                        }
                    },
                    "GRch38": {
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                            "ensembl_id": "ENSG00000104884"
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                    }
                },
                "hgnc_date_symbol_changed": "2001-06-22"
            },
            "entity_type": "gene",
            "entity_name": "ERCC2",
            "confidence_level": "3",
            "penetrance": null,
            "mode_of_pathogenicity": null,
            "publications": [
                "7849702",
                "9758621",
                "11443545",
                "33733458"
            ],
            "evidence": [
                "Expert Review Green",
                "Expert Review"
            ],
            "phenotypes": [
                "Cerebrooculofacioskeletal syndrome 2, MIM# 610756",
                "Trichothiodystrophy 1, photosensitive, MIM# 601675"
            ],
            "mode_of_inheritance": "BIALLELIC, autosomal or pseudoautosomal",
            "tags": [],
            "panel": {
                "id": 3631,
                "hash_id": null,
                "name": "Growth failure",
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                "description": "This panel contains genes associated with growth failure in infancy/early childhood, either isolated or as part of another disorder.\r\n\r\nConsider applying this panel in individuals with:\r\n -Height Standard Deviation Score (SDS) <-3 (very significant short stature - well below the 0.4th centile)\r\nAND at least one of:\r\n- History of small for gestational age (birth weight and/or length <-2SDS)\r\n- Body disproportion, e.g. discrepancy between stature and head size\r\n- Dysmorphic features and congenital anomalies\r\n- Abnormalities in the GH-IGF axis (evidence of GH insensitivity or deficiency) and/or other pituitary hormonal deficiencies\r\n- Family history of significant short stature (1st and 2nd degree relatives) and/or consanguinity\r\n\r\nPrior to genomic testing consider:\r\n-Chromosomal microarray analysis (e.g. Turner syndrome)\r\n-Methylation analysis for Russell-Silver syndrome and Temple syndrome\r\n-Skeletal survey\r\n\r\nAcquired causes of short stature are relatively common.\r\n\r\nDepending on the specific clinical features present, consider applying the Skeletal dysplasia, Intellectual Disability, and/or Pituitary Hormone deficiency panels.\r\n\r\nWith thanks to Genomics England for the original design of this panel.",
                "status": "public",
                "version": "1.102",
                "version_created": "2026-04-01T10:17:12.005431+11:00",
                "relevant_disorders": [
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                    "HP:0001508; Growth delay",
                    "HP:0001510"
                ],
                "stats": {
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                    "number_of_strs": 0,
                    "number_of_regions": 4
                },
                "types": [
                    {
                        "name": "Victorian Clinical Genetics Services",
                        "slug": "victorian-clinical-genetics-services",
                        "description": "Panel used by VCGS."
                    },
                    {
                        "name": "Genetic Health Queensland",
                        "slug": "genetic-health-queensland",
                        "description": "Panel used by GHQ."
                    },
                    {
                        "name": "Royal Melbourne Hospital",
                        "slug": "royal-melbourne-hospital",
                        "description": "Royal Melbourne Hospital"
                    },
                    {
                        "name": "Rare Disease",
                        "slug": "rare-disease",
                        "description": "Rare disease panels"
                    }
                ],
                "child_panel_ids": []
            },
            "transcript": []
        },
        {
            "gene_data": {
                "alias": [],
                "biotype": "protein_coding",
                "hgnc_id": "HGNC:2979",
                "gene_name": "DNA methyltransferase 3 beta",
                "omim_gene": [
                    "602900"
                ],
                "alias_name": null,
                "gene_symbol": "DNMT3B",
                "hgnc_symbol": "DNMT3B",
                "hgnc_release": "2017-11-03",
                "ensembl_genes": {
                    "GRch37": {
                        "82": {
                            "location": "20:31350191-31397162",
                            "ensembl_id": "ENSG00000088305"
                        }
                    },
                    "GRch38": {
                        "90": {
                            "location": "20:32762385-32809356",
                            "ensembl_id": "ENSG00000088305"
                        }
                    }
                },
                "hgnc_date_symbol_changed": "1998-07-15"
            },
            "entity_type": "gene",
            "entity_name": "DNMT3B",
            "confidence_level": "3",
            "penetrance": null,
            "mode_of_pathogenicity": null,
            "publications": [
                "10647011",
                "23486536"
            ],
            "evidence": [
                "Expert Review Green",
                "Expert Review"
            ],
            "phenotypes": [
                "Immunodeficiency-centromeric instability-facial anomalies syndrome 1, MIM#\t242860"
            ],
            "mode_of_inheritance": "BIALLELIC, autosomal or pseudoautosomal",
            "tags": [],
            "panel": {
                "id": 3631,
                "hash_id": null,
                "name": "Growth failure",
                "disease_group": "",
                "disease_sub_group": "",
                "description": "This panel contains genes associated with growth failure in infancy/early childhood, either isolated or as part of another disorder.\r\n\r\nConsider applying this panel in individuals with:\r\n -Height Standard Deviation Score (SDS) <-3 (very significant short stature - well below the 0.4th centile)\r\nAND at least one of:\r\n- History of small for gestational age (birth weight and/or length <-2SDS)\r\n- Body disproportion, e.g. discrepancy between stature and head size\r\n- Dysmorphic features and congenital anomalies\r\n- Abnormalities in the GH-IGF axis (evidence of GH insensitivity or deficiency) and/or other pituitary hormonal deficiencies\r\n- Family history of significant short stature (1st and 2nd degree relatives) and/or consanguinity\r\n\r\nPrior to genomic testing consider:\r\n-Chromosomal microarray analysis (e.g. Turner syndrome)\r\n-Methylation analysis for Russell-Silver syndrome and Temple syndrome\r\n-Skeletal survey\r\n\r\nAcquired causes of short stature are relatively common.\r\n\r\nDepending on the specific clinical features present, consider applying the Skeletal dysplasia, Intellectual Disability, and/or Pituitary Hormone deficiency panels.\r\n\r\nWith thanks to Genomics England for the original design of this panel.",
                "status": "public",
                "version": "1.102",
                "version_created": "2026-04-01T10:17:12.005431+11:00",
                "relevant_disorders": [
                    "Failure to thrive",
                    "HP:0001508; Growth delay",
                    "HP:0001510"
                ],
                "stats": {
                    "number_of_genes": 204,
                    "number_of_strs": 0,
                    "number_of_regions": 4
                },
                "types": [
                    {
                        "name": "Victorian Clinical Genetics Services",
                        "slug": "victorian-clinical-genetics-services",
                        "description": "Panel used by VCGS."
                    },
                    {
                        "name": "Genetic Health Queensland",
                        "slug": "genetic-health-queensland",
                        "description": "Panel used by GHQ."
                    },
                    {
                        "name": "Royal Melbourne Hospital",
                        "slug": "royal-melbourne-hospital",
                        "description": "Royal Melbourne Hospital"
                    },
                    {
                        "name": "Rare Disease",
                        "slug": "rare-disease",
                        "description": "Rare disease panels"
                    }
                ],
                "child_panel_ids": []
            },
            "transcript": []
        },
        {
            "gene_data": {
                "alias": [
                    "CHLR1",
                    "KRG2",
                    "CHL1",
                    "ChlR1",
                    "WABS"
                ],
                "biotype": "protein_coding",
                "hgnc_id": "HGNC:2736",
                "gene_name": "DEAD/H-box helicase 11",
                "omim_gene": [
                    "601150"
                ],
                "alias_name": [
                    "CHL1-like helicase homolog (S. cerevisiae)"
                ],
                "gene_symbol": "DDX11",
                "hgnc_symbol": "DDX11",
                "hgnc_release": "2017-11-03",
                "ensembl_genes": {
                    "GRch37": {
                        "82": {
                            "location": "12:31226779-31257725",
                            "ensembl_id": "ENSG00000013573"
                        }
                    },
                    "GRch38": {
                        "90": {
                            "location": "12:31073845-31104791",
                            "ensembl_id": "ENSG00000013573"
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                    }
                },
                "hgnc_date_symbol_changed": "1995-12-11"
            },
            "entity_type": "gene",
            "entity_name": "DDX11",
            "confidence_level": "3",
            "penetrance": null,
            "mode_of_pathogenicity": null,
            "publications": [
                "20137776, 23033317, 30216658, 30924321, 32855419, 36703504, 26089203"
            ],
            "evidence": [
                "Expert Review Green",
                "Expert Review"
            ],
            "phenotypes": [
                "Warsaw breakage syndrome, MONDO:0013252"
            ],
            "mode_of_inheritance": "BIALLELIC, autosomal or pseudoautosomal",
            "tags": [],
            "panel": {
                "id": 3631,
                "hash_id": null,
                "name": "Growth failure",
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                "disease_sub_group": "",
                "description": "This panel contains genes associated with growth failure in infancy/early childhood, either isolated or as part of another disorder.\r\n\r\nConsider applying this panel in individuals with:\r\n -Height Standard Deviation Score (SDS) <-3 (very significant short stature - well below the 0.4th centile)\r\nAND at least one of:\r\n- History of small for gestational age (birth weight and/or length <-2SDS)\r\n- Body disproportion, e.g. discrepancy between stature and head size\r\n- Dysmorphic features and congenital anomalies\r\n- Abnormalities in the GH-IGF axis (evidence of GH insensitivity or deficiency) and/or other pituitary hormonal deficiencies\r\n- Family history of significant short stature (1st and 2nd degree relatives) and/or consanguinity\r\n\r\nPrior to genomic testing consider:\r\n-Chromosomal microarray analysis (e.g. Turner syndrome)\r\n-Methylation analysis for Russell-Silver syndrome and Temple syndrome\r\n-Skeletal survey\r\n\r\nAcquired causes of short stature are relatively common.\r\n\r\nDepending on the specific clinical features present, consider applying the Skeletal dysplasia, Intellectual Disability, and/or Pituitary Hormone deficiency panels.\r\n\r\nWith thanks to Genomics England for the original design of this panel.",
                "status": "public",
                "version": "1.102",
                "version_created": "2026-04-01T10:17:12.005431+11:00",
                "relevant_disorders": [
                    "Failure to thrive",
                    "HP:0001508; Growth delay",
                    "HP:0001510"
                ],
                "stats": {
                    "number_of_genes": 204,
                    "number_of_strs": 0,
                    "number_of_regions": 4
                },
                "types": [
                    {
                        "name": "Victorian Clinical Genetics Services",
                        "slug": "victorian-clinical-genetics-services",
                        "description": "Panel used by VCGS."
                    },
                    {
                        "name": "Genetic Health Queensland",
                        "slug": "genetic-health-queensland",
                        "description": "Panel used by GHQ."
                    },
                    {
                        "name": "Royal Melbourne Hospital",
                        "slug": "royal-melbourne-hospital",
                        "description": "Royal Melbourne Hospital"
                    },
                    {
                        "name": "Rare Disease",
                        "slug": "rare-disease",
                        "description": "Rare disease panels"
                    }
                ],
                "child_panel_ids": []
            },
            "transcript": []
        },
        {
            "gene_data": {
                "alias": [
                    "RNF53",
                    "BRCC1",
                    "PPP1R53",
                    "FANCS"
                ],
                "biotype": "protein_coding",
                "hgnc_id": "HGNC:1100",
                "gene_name": "BRCA1, DNA repair associated",
                "omim_gene": [
                    "113705"
                ],
                "alias_name": [
                    "BRCA1/BRCA2-containing complex, subunit 1",
                    "protein phosphatase 1, regulatory subunit 53",
                    "Fanconi anemia, complementation group S"
                ],
                "gene_symbol": "BRCA1",
                "hgnc_symbol": "BRCA1",
                "hgnc_release": "2017-11-03",
                "ensembl_genes": {
                    "GRch37": {
                        "82": {
                            "location": "17:41196312-41277500",
                            "ensembl_id": "ENSG00000012048"
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                    },
                    "GRch38": {
                        "90": {
                            "location": "17:43044295-43170245",
                            "ensembl_id": "ENSG00000012048"
                        }
                    }
                },
                "hgnc_date_symbol_changed": "1991-02-20"
            },
            "entity_type": "gene",
            "entity_name": "BRCA1",
            "confidence_level": "3",
            "penetrance": null,
            "mode_of_pathogenicity": null,
            "publications": [
                "23269703",
                "29133208",
                "25472942",
                "29712865"
            ],
            "evidence": [
                "Expert Review Green",
                "Expert list"
            ],
            "phenotypes": [
                "Fanconi anaemia, complementation group S, MIM#\t617883"
            ],
            "mode_of_inheritance": "BIALLELIC, autosomal or pseudoautosomal",
            "tags": [],
            "panel": {
                "id": 3631,
                "hash_id": null,
                "name": "Growth failure",
                "disease_group": "",
                "disease_sub_group": "",
                "description": "This panel contains genes associated with growth failure in infancy/early childhood, either isolated or as part of another disorder.\r\n\r\nConsider applying this panel in individuals with:\r\n -Height Standard Deviation Score (SDS) <-3 (very significant short stature - well below the 0.4th centile)\r\nAND at least one of:\r\n- History of small for gestational age (birth weight and/or length <-2SDS)\r\n- Body disproportion, e.g. discrepancy between stature and head size\r\n- Dysmorphic features and congenital anomalies\r\n- Abnormalities in the GH-IGF axis (evidence of GH insensitivity or deficiency) and/or other pituitary hormonal deficiencies\r\n- Family history of significant short stature (1st and 2nd degree relatives) and/or consanguinity\r\n\r\nPrior to genomic testing consider:\r\n-Chromosomal microarray analysis (e.g. Turner syndrome)\r\n-Methylation analysis for Russell-Silver syndrome and Temple syndrome\r\n-Skeletal survey\r\n\r\nAcquired causes of short stature are relatively common.\r\n\r\nDepending on the specific clinical features present, consider applying the Skeletal dysplasia, Intellectual Disability, and/or Pituitary Hormone deficiency panels.\r\n\r\nWith thanks to Genomics England for the original design of this panel.",
                "status": "public",
                "version": "1.102",
                "version_created": "2026-04-01T10:17:12.005431+11:00",
                "relevant_disorders": [
                    "Failure to thrive",
                    "HP:0001508; Growth delay",
                    "HP:0001510"
                ],
                "stats": {
                    "number_of_genes": 204,
                    "number_of_strs": 0,
                    "number_of_regions": 4
                },
                "types": [
                    {
                        "name": "Victorian Clinical Genetics Services",
                        "slug": "victorian-clinical-genetics-services",
                        "description": "Panel used by VCGS."
                    },
                    {
                        "name": "Genetic Health Queensland",
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                    },
                    {
                        "name": "Royal Melbourne Hospital",
                        "slug": "royal-melbourne-hospital",
                        "description": "Royal Melbourne Hospital"
                    },
                    {
                        "name": "Rare Disease",
                        "slug": "rare-disease",
                        "description": "Rare disease panels"
                    }
                ],
                "child_panel_ids": []
            },
            "transcript": []
        },
        {
            "gene_data": {
                "alias": [
                    "TEL1",
                    "TELO1"
                ],
                "biotype": "protein_coding",
                "hgnc_id": "HGNC:795",
                "gene_name": "ATM serine/threonine kinase",
                "omim_gene": [
                    "607585"
                ],
                "alias_name": [
                    "TEL1, telomere maintenance 1, homolog (S. cerevisiae)"
                ],
                "gene_symbol": "ATM",
                "hgnc_symbol": "ATM",
                "hgnc_release": "2017-11-03",
                "ensembl_genes": {
                    "GRch37": {
                        "82": {
                            "location": "11:108093211-108239829",
                            "ensembl_id": "ENSG00000149311"
                        }
                    },
                    "GRch38": {
                        "90": {
                            "location": "11:108222484-108369102",
                            "ensembl_id": "ENSG00000149311"
                        }
                    }
                },
                "hgnc_date_symbol_changed": "1995-07-07"
            },
            "entity_type": "gene",
            "entity_name": "ATM",
            "confidence_level": "3",
            "penetrance": null,
            "mode_of_pathogenicity": null,
            "publications": [
                "30137827"
            ],
            "evidence": [
                "Expert Review Green",
                "Expert Review"
            ],
            "phenotypes": [
                "Ataxia-telangiectasia, MIM# 208900"
            ],
            "mode_of_inheritance": "BIALLELIC, autosomal or pseudoautosomal",
            "tags": [],
            "panel": {
                "id": 3631,
                "hash_id": null,
                "name": "Growth failure",
                "disease_group": "",
                "disease_sub_group": "",
                "description": "This panel contains genes associated with growth failure in infancy/early childhood, either isolated or as part of another disorder.\r\n\r\nConsider applying this panel in individuals with:\r\n -Height Standard Deviation Score (SDS) <-3 (very significant short stature - well below the 0.4th centile)\r\nAND at least one of:\r\n- History of small for gestational age (birth weight and/or length <-2SDS)\r\n- Body disproportion, e.g. discrepancy between stature and head size\r\n- Dysmorphic features and congenital anomalies\r\n- Abnormalities in the GH-IGF axis (evidence of GH insensitivity or deficiency) and/or other pituitary hormonal deficiencies\r\n- Family history of significant short stature (1st and 2nd degree relatives) and/or consanguinity\r\n\r\nPrior to genomic testing consider:\r\n-Chromosomal microarray analysis (e.g. Turner syndrome)\r\n-Methylation analysis for Russell-Silver syndrome and Temple syndrome\r\n-Skeletal survey\r\n\r\nAcquired causes of short stature are relatively common.\r\n\r\nDepending on the specific clinical features present, consider applying the Skeletal dysplasia, Intellectual Disability, and/or Pituitary Hormone deficiency panels.\r\n\r\nWith thanks to Genomics England for the original design of this panel.",
                "status": "public",
                "version": "1.102",
                "version_created": "2026-04-01T10:17:12.005431+11:00",
                "relevant_disorders": [
                    "Failure to thrive",
                    "HP:0001508; Growth delay",
                    "HP:0001510"
                ],
                "stats": {
                    "number_of_genes": 204,
                    "number_of_strs": 0,
                    "number_of_regions": 4
                },
                "types": [
                    {
                        "name": "Victorian Clinical Genetics Services",
                        "slug": "victorian-clinical-genetics-services",
                        "description": "Panel used by VCGS."
                    },
                    {
                        "name": "Genetic Health Queensland",
                        "slug": "genetic-health-queensland",
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                    {
                        "name": "Royal Melbourne Hospital",
                        "slug": "royal-melbourne-hospital",
                        "description": "Royal Melbourne Hospital"
                    },
                    {
                        "name": "Rare Disease",
                        "slug": "rare-disease",
                        "description": "Rare disease panels"
                    }
                ],
                "child_panel_ids": []
            },
            "transcript": []
        },
        {
            "gene_data": {
                "alias": [
                    "JTK13",
                    "CD221",
                    "IGFIR",
                    "MGC18216",
                    "IGFR"
                ],
                "biotype": "protein_coding",
                "hgnc_id": "HGNC:5465",
                "gene_name": "insulin like growth factor 1 receptor",
                "omim_gene": [
                    "147370"
                ],
                "alias_name": null,
                "gene_symbol": "IGF1R",
                "hgnc_symbol": "IGF1R",
                "hgnc_release": "2017-11-03",
                "ensembl_genes": {
                    "GRch37": {
                        "82": {
                            "location": "15:99192200-99507759",
                            "ensembl_id": "ENSG00000140443"
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                    },
                    "GRch38": {
                        "90": {
                            "location": "15:98648971-98964530",
                            "ensembl_id": "ENSG00000140443"
                        }
                    }
                },
                "hgnc_date_symbol_changed": "1988-07-07"
            },
            "entity_type": "gene",
            "entity_name": "IGF1R",
            "confidence_level": "3",
            "penetrance": null,
            "mode_of_pathogenicity": "",
            "publications": [
                "14657428",
                "22130793",
                "23045302",
                "26252249",
                "17264177",
                "31586944"
            ],
            "evidence": [
                "Expert Review Green",
                "Genomics England PanelApp"
            ],
            "phenotypes": [
                "Insulin-like growth factor I, resistance to, MIM # 270450"
            ],
            "mode_of_inheritance": "BOTH monoallelic and biallelic, autosomal or pseudoautosomal",
            "tags": [],
            "panel": {
                "id": 3631,
                "hash_id": null,
                "name": "Growth failure",
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                "disease_sub_group": "",
                "description": "This panel contains genes associated with growth failure in infancy/early childhood, either isolated or as part of another disorder.\r\n\r\nConsider applying this panel in individuals with:\r\n -Height Standard Deviation Score (SDS) <-3 (very significant short stature - well below the 0.4th centile)\r\nAND at least one of:\r\n- History of small for gestational age (birth weight and/or length <-2SDS)\r\n- Body disproportion, e.g. discrepancy between stature and head size\r\n- Dysmorphic features and congenital anomalies\r\n- Abnormalities in the GH-IGF axis (evidence of GH insensitivity or deficiency) and/or other pituitary hormonal deficiencies\r\n- Family history of significant short stature (1st and 2nd degree relatives) and/or consanguinity\r\n\r\nPrior to genomic testing consider:\r\n-Chromosomal microarray analysis (e.g. Turner syndrome)\r\n-Methylation analysis for Russell-Silver syndrome and Temple syndrome\r\n-Skeletal survey\r\n\r\nAcquired causes of short stature are relatively common.\r\n\r\nDepending on the specific clinical features present, consider applying the Skeletal dysplasia, Intellectual Disability, and/or Pituitary Hormone deficiency panels.\r\n\r\nWith thanks to Genomics England for the original design of this panel.",
                "status": "public",
                "version": "1.102",
                "version_created": "2026-04-01T10:17:12.005431+11:00",
                "relevant_disorders": [
                    "Failure to thrive",
                    "HP:0001508; Growth delay",
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                ],
                "stats": {
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                    "number_of_strs": 0,
                    "number_of_regions": 4
                },
                "types": [
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                        "name": "Victorian Clinical Genetics Services",
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                        "slug": "rare-disease",
                        "description": "Rare disease panels"
                    }
                ],
                "child_panel_ids": []
            },
            "transcript": null
        },
        {
            "gene_data": {
                "alias": [
                    "TRIP",
                    "RNF206"
                ],
                "biotype": "protein_coding",
                "hgnc_id": "HGNC:30764",
                "gene_name": "TRAF interacting protein",
                "omim_gene": [
                    "605958"
                ],
                "alias_name": [
                    "ring finger protein 206"
                ],
                "gene_symbol": "TRAIP",
                "hgnc_symbol": "TRAIP",
                "hgnc_release": "2017-11-03",
                "ensembl_genes": {
                    "GRch37": {
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                            "location": "3:49866034-49894007",
                            "ensembl_id": "ENSG00000183763"
                        }
                    },
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                            "location": "3:49828599-49856574",
                            "ensembl_id": "ENSG00000183763"
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                    }
                },
                "hgnc_date_symbol_changed": "2006-01-09"
            },
            "entity_type": "gene",
            "entity_name": "TRAIP",
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            "penetrance": null,
            "mode_of_pathogenicity": null,
            "publications": [
                "26595769"
            ],
            "evidence": [
                "Expert Review Green",
                "Expert Review"
            ],
            "phenotypes": [
                "Seckel syndrome 9, MIM# 616777"
            ],
            "mode_of_inheritance": "BIALLELIC, autosomal or pseudoautosomal",
            "tags": [],
            "panel": {
                "id": 3631,
                "hash_id": null,
                "name": "Growth failure",
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                "description": "This panel contains genes associated with growth failure in infancy/early childhood, either isolated or as part of another disorder.\r\n\r\nConsider applying this panel in individuals with:\r\n -Height Standard Deviation Score (SDS) <-3 (very significant short stature - well below the 0.4th centile)\r\nAND at least one of:\r\n- History of small for gestational age (birth weight and/or length <-2SDS)\r\n- Body disproportion, e.g. discrepancy between stature and head size\r\n- Dysmorphic features and congenital anomalies\r\n- Abnormalities in the GH-IGF axis (evidence of GH insensitivity or deficiency) and/or other pituitary hormonal deficiencies\r\n- Family history of significant short stature (1st and 2nd degree relatives) and/or consanguinity\r\n\r\nPrior to genomic testing consider:\r\n-Chromosomal microarray analysis (e.g. Turner syndrome)\r\n-Methylation analysis for Russell-Silver syndrome and Temple syndrome\r\n-Skeletal survey\r\n\r\nAcquired causes of short stature are relatively common.\r\n\r\nDepending on the specific clinical features present, consider applying the Skeletal dysplasia, Intellectual Disability, and/or Pituitary Hormone deficiency panels.\r\n\r\nWith thanks to Genomics England for the original design of this panel.",
                "status": "public",
                "version": "1.102",
                "version_created": "2026-04-01T10:17:12.005431+11:00",
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                    "HP:0001508; Growth delay",
                    "HP:0001510"
                ],
                "stats": {
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                    "number_of_strs": 0,
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                },
                "types": [
                    {
                        "name": "Victorian Clinical Genetics Services",
                        "slug": "victorian-clinical-genetics-services",
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                    {
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                    {
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                    {
                        "name": "Rare Disease",
                        "slug": "rare-disease",
                        "description": "Rare disease panels"
                    }
                ],
                "child_panel_ids": []
            },
            "transcript": []
        },
        {
            "gene_data": {
                "alias": [
                    "POLE1"
                ],
                "biotype": "protein_coding",
                "hgnc_id": "HGNC:9177",
                "gene_name": "DNA polymerase epsilon, catalytic subunit",
                "omim_gene": [
                    "174762"
                ],
                "alias_name": [
                    "DNA polymerase epsilon catalytic subunit A"
                ],
                "gene_symbol": "POLE",
                "hgnc_symbol": "POLE",
                "hgnc_release": "2017-11-03",
                "ensembl_genes": {
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                            "location": "12:133200348-133263951",
                            "ensembl_id": "ENSG00000177084"
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                    },
                    "GRch38": {
                        "90": {
                            "location": "12:132623753-132687365",
                            "ensembl_id": "ENSG00000177084"
                        }
                    }
                },
                "hgnc_date_symbol_changed": "1992-02-06"
            },
            "entity_type": "gene",
            "entity_name": "POLE",
            "confidence_level": "3",
            "penetrance": null,
            "mode_of_pathogenicity": null,
            "publications": [
                "30503519",
                "23230001",
                "25948378"
            ],
            "evidence": [
                "Expert Review Green",
                "Expert Review"
            ],
            "phenotypes": [
                "FILS syndrome, MIM# 615139",
                "IMAGE-I syndrome, MIM# 618336"
            ],
            "mode_of_inheritance": "BIALLELIC, autosomal or pseudoautosomal",
            "tags": [
                "deep intronic"
            ],
            "panel": {
                "id": 3631,
                "hash_id": null,
                "name": "Growth failure",
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                "disease_sub_group": "",
                "description": "This panel contains genes associated with growth failure in infancy/early childhood, either isolated or as part of another disorder.\r\n\r\nConsider applying this panel in individuals with:\r\n -Height Standard Deviation Score (SDS) <-3 (very significant short stature - well below the 0.4th centile)\r\nAND at least one of:\r\n- History of small for gestational age (birth weight and/or length <-2SDS)\r\n- Body disproportion, e.g. discrepancy between stature and head size\r\n- Dysmorphic features and congenital anomalies\r\n- Abnormalities in the GH-IGF axis (evidence of GH insensitivity or deficiency) and/or other pituitary hormonal deficiencies\r\n- Family history of significant short stature (1st and 2nd degree relatives) and/or consanguinity\r\n\r\nPrior to genomic testing consider:\r\n-Chromosomal microarray analysis (e.g. Turner syndrome)\r\n-Methylation analysis for Russell-Silver syndrome and Temple syndrome\r\n-Skeletal survey\r\n\r\nAcquired causes of short stature are relatively common.\r\n\r\nDepending on the specific clinical features present, consider applying the Skeletal dysplasia, Intellectual Disability, and/or Pituitary Hormone deficiency panels.\r\n\r\nWith thanks to Genomics England for the original design of this panel.",
                "status": "public",
                "version": "1.102",
                "version_created": "2026-04-01T10:17:12.005431+11:00",
                "relevant_disorders": [
                    "Failure to thrive",
                    "HP:0001508; Growth delay",
                    "HP:0001510"
                ],
                "stats": {
                    "number_of_genes": 204,
                    "number_of_strs": 0,
                    "number_of_regions": 4
                },
                "types": [
                    {
                        "name": "Victorian Clinical Genetics Services",
                        "slug": "victorian-clinical-genetics-services",
                        "description": "Panel used by VCGS."
                    },
                    {
                        "name": "Genetic Health Queensland",
                        "slug": "genetic-health-queensland",
                        "description": "Panel used by GHQ."
                    },
                    {
                        "name": "Royal Melbourne Hospital",
                        "slug": "royal-melbourne-hospital",
                        "description": "Royal Melbourne Hospital"
                    },
                    {
                        "name": "Rare Disease",
                        "slug": "rare-disease",
                        "description": "Rare disease panels"
                    }
                ],
                "child_panel_ids": []
            },
            "transcript": []
        },
        {
            "gene_data": {
                "alias": [
                    "HDCMA18P",
                    "PIP7S",
                    "DKFZP564K112"
                ],
                "biotype": "protein_coding",
                "hgnc_id": "HGNC:24912",
                "gene_name": "La ribonucleoprotein domain family member 7",
                "omim_gene": [
                    "612026"
                ],
                "alias_name": [
                    "P-TEFb-interaction protein for 7SK stability"
                ],
                "gene_symbol": "LARP7",
                "hgnc_symbol": "LARP7",
                "hgnc_release": "2017-11-03",
                "ensembl_genes": {
                    "GRch37": {
                        "82": {
                            "location": "4:113558120-113578748",
                            "ensembl_id": "ENSG00000174720"
                        }
                    },
                    "GRch38": {
                        "90": {
                            "location": "4:112636964-112657592",
                            "ensembl_id": "ENSG00000174720"
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                    }
                },
                "hgnc_date_symbol_changed": "2006-07-05"
            },
            "entity_type": "gene",
            "entity_name": "LARP7",
            "confidence_level": "3",
            "penetrance": null,
            "mode_of_pathogenicity": null,
            "publications": [
                "22865833",
                "21937992",
                "30006060",
                "33569879"
            ],
            "evidence": [
                "Expert Review Green",
                "Expert Review"
            ],
            "phenotypes": [
                "Alazami syndrome, MIM# 615071",
                "Microcephalic primordial dwarfism, Alazami type MONDO:0014031"
            ],
            "mode_of_inheritance": "BIALLELIC, autosomal or pseudoautosomal",
            "tags": [],
            "panel": {
                "id": 3631,
                "hash_id": null,
                "name": "Growth failure",
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                "description": "This panel contains genes associated with growth failure in infancy/early childhood, either isolated or as part of another disorder.\r\n\r\nConsider applying this panel in individuals with:\r\n -Height Standard Deviation Score (SDS) <-3 (very significant short stature - well below the 0.4th centile)\r\nAND at least one of:\r\n- History of small for gestational age (birth weight and/or length <-2SDS)\r\n- Body disproportion, e.g. discrepancy between stature and head size\r\n- Dysmorphic features and congenital anomalies\r\n- Abnormalities in the GH-IGF axis (evidence of GH insensitivity or deficiency) and/or other pituitary hormonal deficiencies\r\n- Family history of significant short stature (1st and 2nd degree relatives) and/or consanguinity\r\n\r\nPrior to genomic testing consider:\r\n-Chromosomal microarray analysis (e.g. Turner syndrome)\r\n-Methylation analysis for Russell-Silver syndrome and Temple syndrome\r\n-Skeletal survey\r\n\r\nAcquired causes of short stature are relatively common.\r\n\r\nDepending on the specific clinical features present, consider applying the Skeletal dysplasia, Intellectual Disability, and/or Pituitary Hormone deficiency panels.\r\n\r\nWith thanks to Genomics England for the original design of this panel.",
                "status": "public",
                "version": "1.102",
                "version_created": "2026-04-01T10:17:12.005431+11:00",
                "relevant_disorders": [
                    "Failure to thrive",
                    "HP:0001508; Growth delay",
                    "HP:0001510"
                ],
                "stats": {
                    "number_of_genes": 204,
                    "number_of_strs": 0,
                    "number_of_regions": 4
                },
                "types": [
                    {
                        "name": "Victorian Clinical Genetics Services",
                        "slug": "victorian-clinical-genetics-services",
                        "description": "Panel used by VCGS."
                    },
                    {
                        "name": "Genetic Health Queensland",
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                        "description": "Panel used by GHQ."
                    },
                    {
                        "name": "Royal Melbourne Hospital",
                        "slug": "royal-melbourne-hospital",
                        "description": "Royal Melbourne Hospital"
                    },
                    {
                        "name": "Rare Disease",
                        "slug": "rare-disease",
                        "description": "Rare disease panels"
                    }
                ],
                "child_panel_ids": []
            },
            "transcript": []
        },
        {
            "gene_data": {
                "alias": [
                    "FLJ22794",
                    "KIAA1895"
                ],
                "biotype": "protein_coding",
                "hgnc_id": "HGNC:24725",
                "gene_name": "family with sequence similarity 111 member A",
                "omim_gene": [
                    "615292"
                ],
                "alias_name": null,
                "gene_symbol": "FAM111A",
                "hgnc_symbol": "FAM111A",
                "hgnc_release": "2017-11-03",
                "ensembl_genes": {
                    "GRch37": {
                        "82": {
                            "location": "11:58910221-58922512",
                            "ensembl_id": "ENSG00000166801"
                        }
                    },
                    "GRch38": {
                        "90": {
                            "location": "11:59142748-59155039",
                            "ensembl_id": "ENSG00000166801"
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                    }
                },
                "hgnc_date_symbol_changed": "2006-02-06"
            },
            "entity_type": "gene",
            "entity_name": "FAM111A",
            "confidence_level": "3",
            "penetrance": null,
            "mode_of_pathogenicity": null,
            "publications": [
                "32996714",
                "23684011"
            ],
            "evidence": [
                "Expert Review Green",
                "Expert Review"
            ],
            "phenotypes": [
                "Kenny-Caffey syndrome, type 2, MIM@\t127000"
            ],
            "mode_of_inheritance": "MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted",
            "tags": [],
            "panel": {
                "id": 3631,
                "hash_id": null,
                "name": "Growth failure",
                "disease_group": "",
                "disease_sub_group": "",
                "description": "This panel contains genes associated with growth failure in infancy/early childhood, either isolated or as part of another disorder.\r\n\r\nConsider applying this panel in individuals with:\r\n -Height Standard Deviation Score (SDS) <-3 (very significant short stature - well below the 0.4th centile)\r\nAND at least one of:\r\n- History of small for gestational age (birth weight and/or length <-2SDS)\r\n- Body disproportion, e.g. discrepancy between stature and head size\r\n- Dysmorphic features and congenital anomalies\r\n- Abnormalities in the GH-IGF axis (evidence of GH insensitivity or deficiency) and/or other pituitary hormonal deficiencies\r\n- Family history of significant short stature (1st and 2nd degree relatives) and/or consanguinity\r\n\r\nPrior to genomic testing consider:\r\n-Chromosomal microarray analysis (e.g. Turner syndrome)\r\n-Methylation analysis for Russell-Silver syndrome and Temple syndrome\r\n-Skeletal survey\r\n\r\nAcquired causes of short stature are relatively common.\r\n\r\nDepending on the specific clinical features present, consider applying the Skeletal dysplasia, Intellectual Disability, and/or Pituitary Hormone deficiency panels.\r\n\r\nWith thanks to Genomics England for the original design of this panel.",
                "status": "public",
                "version": "1.102",
                "version_created": "2026-04-01T10:17:12.005431+11:00",
                "relevant_disorders": [
                    "Failure to thrive",
                    "HP:0001508; Growth delay",
                    "HP:0001510"
                ],
                "stats": {
                    "number_of_genes": 204,
                    "number_of_strs": 0,
                    "number_of_regions": 4
                },
                "types": [
                    {
                        "name": "Victorian Clinical Genetics Services",
                        "slug": "victorian-clinical-genetics-services",
                        "description": "Panel used by VCGS."
                    },
                    {
                        "name": "Genetic Health Queensland",
                        "slug": "genetic-health-queensland",
                        "description": "Panel used by GHQ."
                    },
                    {
                        "name": "Royal Melbourne Hospital",
                        "slug": "royal-melbourne-hospital",
                        "description": "Royal Melbourne Hospital"
                    },
                    {
                        "name": "Rare Disease",
                        "slug": "rare-disease",
                        "description": "Rare disease panels"
                    }
                ],
                "child_panel_ids": []
            },
            "transcript": []
        },
        {
            "gene_data": {
                "alias": [
                    "LGCR",
                    "GC79"
                ],
                "biotype": "protein_coding",
                "hgnc_id": "HGNC:12340",
                "gene_name": "transcriptional repressor GATA binding 1",
                "omim_gene": [
                    "604386"
                ],
                "alias_name": null,
                "gene_symbol": "TRPS1",
                "hgnc_symbol": "TRPS1",
                "hgnc_release": "2017-11-03",
                "ensembl_genes": {
                    "GRch37": {
                        "82": {
                            "location": "8:116420724-116821899",
                            "ensembl_id": "ENSG00000104447"
                        }
                    },
                    "GRch38": {
                        "90": {
                            "location": "8:115408496-115809673",
                            "ensembl_id": "ENSG00000104447"
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                    }
                },
                "hgnc_date_symbol_changed": "1995-07-06"
            },
            "entity_type": "gene",
            "entity_name": "TRPS1",
            "confidence_level": "3",
            "penetrance": null,
            "mode_of_pathogenicity": null,
            "publications": [
                "11112658",
                "10615131"
            ],
            "evidence": [
                "Expert Review Green",
                "Literature"
            ],
            "phenotypes": [
                "Trichorhinophalangeal syndrome, type I, OMIM # 190350",
                "Trichorhinophalangeal syndrome, type III, OMIM # 190351"
            ],
            "mode_of_inheritance": "MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted",
            "tags": [],
            "panel": {
                "id": 3631,
                "hash_id": null,
                "name": "Growth failure",
                "disease_group": "",
                "disease_sub_group": "",
                "description": "This panel contains genes associated with growth failure in infancy/early childhood, either isolated or as part of another disorder.\r\n\r\nConsider applying this panel in individuals with:\r\n -Height Standard Deviation Score (SDS) <-3 (very significant short stature - well below the 0.4th centile)\r\nAND at least one of:\r\n- History of small for gestational age (birth weight and/or length <-2SDS)\r\n- Body disproportion, e.g. discrepancy between stature and head size\r\n- Dysmorphic features and congenital anomalies\r\n- Abnormalities in the GH-IGF axis (evidence of GH insensitivity or deficiency) and/or other pituitary hormonal deficiencies\r\n- Family history of significant short stature (1st and 2nd degree relatives) and/or consanguinity\r\n\r\nPrior to genomic testing consider:\r\n-Chromosomal microarray analysis (e.g. Turner syndrome)\r\n-Methylation analysis for Russell-Silver syndrome and Temple syndrome\r\n-Skeletal survey\r\n\r\nAcquired causes of short stature are relatively common.\r\n\r\nDepending on the specific clinical features present, consider applying the Skeletal dysplasia, Intellectual Disability, and/or Pituitary Hormone deficiency panels.\r\n\r\nWith thanks to Genomics England for the original design of this panel.",
                "status": "public",
                "version": "1.102",
                "version_created": "2026-04-01T10:17:12.005431+11:00",
                "relevant_disorders": [
                    "Failure to thrive",
                    "HP:0001508; Growth delay",
                    "HP:0001510"
                ],
                "stats": {
                    "number_of_genes": 204,
                    "number_of_strs": 0,
                    "number_of_regions": 4
                },
                "types": [
                    {
                        "name": "Victorian Clinical Genetics Services",
                        "slug": "victorian-clinical-genetics-services",
                        "description": "Panel used by VCGS."
                    },
                    {
                        "name": "Genetic Health Queensland",
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                    {
                        "name": "Royal Melbourne Hospital",
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                    },
                    {
                        "name": "Rare Disease",
                        "slug": "rare-disease",
                        "description": "Rare disease panels"
                    }
                ],
                "child_panel_ids": []
            },
            "transcript": []
        },
        {
            "gene_data": {
                "alias": [
                    "FIR",
                    "SIAHBP1",
                    "RoBPI"
                ],
                "biotype": "protein_coding",
                "hgnc_id": "HGNC:17042",
                "gene_name": "poly(U) binding splicing factor 60",
                "omim_gene": [
                    "604819"
                ],
                "alias_name": [
                    "siah binding protein 1",
                    "FBP interacting repressor",
                    "pyrimidine tract binding splicing factor",
                    "Ro ribonucleoprotein binding protein 1"
                ],
                "gene_symbol": "PUF60",
                "hgnc_symbol": "PUF60",
                "hgnc_release": "2017-11-03",
                "ensembl_genes": {
                    "GRch37": {
                        "82": {
                            "location": "8:144898514-144912029",
                            "ensembl_id": "ENSG00000179950"
                        }
                    },
                    "GRch38": {
                        "90": {
                            "location": "8:143816344-143829859",
                            "ensembl_id": "ENSG00000179950"
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                    }
                },
                "hgnc_date_symbol_changed": "2007-07-27"
            },
            "entity_type": "gene",
            "entity_name": "PUF60",
            "confidence_level": "3",
            "penetrance": null,
            "mode_of_pathogenicity": null,
            "publications": [
                "19464398",
                "24140112",
                "28327570",
                "27804958"
            ],
            "evidence": [
                "Expert Review Green",
                "Literature"
            ],
            "phenotypes": [
                "Verheij syndrome, OMIM # 615583"
            ],
            "mode_of_inheritance": "MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted",
            "tags": [],
            "panel": {
                "id": 3631,
                "hash_id": null,
                "name": "Growth failure",
                "disease_group": "",
                "disease_sub_group": "",
                "description": "This panel contains genes associated with growth failure in infancy/early childhood, either isolated or as part of another disorder.\r\n\r\nConsider applying this panel in individuals with:\r\n -Height Standard Deviation Score (SDS) <-3 (very significant short stature - well below the 0.4th centile)\r\nAND at least one of:\r\n- History of small for gestational age (birth weight and/or length <-2SDS)\r\n- Body disproportion, e.g. discrepancy between stature and head size\r\n- Dysmorphic features and congenital anomalies\r\n- Abnormalities in the GH-IGF axis (evidence of GH insensitivity or deficiency) and/or other pituitary hormonal deficiencies\r\n- Family history of significant short stature (1st and 2nd degree relatives) and/or consanguinity\r\n\r\nPrior to genomic testing consider:\r\n-Chromosomal microarray analysis (e.g. Turner syndrome)\r\n-Methylation analysis for Russell-Silver syndrome and Temple syndrome\r\n-Skeletal survey\r\n\r\nAcquired causes of short stature are relatively common.\r\n\r\nDepending on the specific clinical features present, consider applying the Skeletal dysplasia, Intellectual Disability, and/or Pituitary Hormone deficiency panels.\r\n\r\nWith thanks to Genomics England for the original design of this panel.",
                "status": "public",
                "version": "1.102",
                "version_created": "2026-04-01T10:17:12.005431+11:00",
                "relevant_disorders": [
                    "Failure to thrive",
                    "HP:0001508; Growth delay",
                    "HP:0001510"
                ],
                "stats": {
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                    "number_of_strs": 0,
                    "number_of_regions": 4
                },
                "types": [
                    {
                        "name": "Victorian Clinical Genetics Services",
                        "slug": "victorian-clinical-genetics-services",
                        "description": "Panel used by VCGS."
                    },
                    {
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                    },
                    {
                        "name": "Rare Disease",
                        "slug": "rare-disease",
                        "description": "Rare disease panels"
                    }
                ],
                "child_panel_ids": []
            },
            "transcript": []
        },
        {
            "gene_data": {
                "alias": [
                    "HUNKI",
                    "MCAP",
                    "CAP",
                    "HUNK1"
                ],
                "biotype": "protein_coding",
                "hgnc_id": "HGNC:13575",
                "gene_name": "bromodomain containing 4",
                "omim_gene": [
                    "608749"
                ],
                "alias_name": [
                    "chromosome-associated protein"
                ],
                "gene_symbol": "BRD4",
                "hgnc_symbol": "BRD4",
                "hgnc_release": "2017-11-03",
                "ensembl_genes": {
                    "GRch37": {
                        "82": {
                            "location": "19:15347647-15443356",
                            "ensembl_id": "ENSG00000141867"
                        }
                    },
                    "GRch38": {
                        "90": {
                            "location": "19:15235519-15332545",
                            "ensembl_id": "ENSG00000141867"
                        }
                    }
                },
                "hgnc_date_symbol_changed": "2000-09-26"
            },
            "entity_type": "gene",
            "entity_name": "BRD4",
            "confidence_level": "3",
            "penetrance": null,
            "mode_of_pathogenicity": null,
            "publications": [
                "29379197",
                "30302754",
                "11997514",
                "34035299"
            ],
            "evidence": [
                "Expert Review Green",
                "Literature"
            ],
            "phenotypes": [
                "Cornelia de Lange syndrome, MONDO:0016033"
            ],
            "mode_of_inheritance": "MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted",
            "tags": [],
            "panel": {
                "id": 3631,
                "hash_id": null,
                "name": "Growth failure",
                "disease_group": "",
                "disease_sub_group": "",
                "description": "This panel contains genes associated with growth failure in infancy/early childhood, either isolated or as part of another disorder.\r\n\r\nConsider applying this panel in individuals with:\r\n -Height Standard Deviation Score (SDS) <-3 (very significant short stature - well below the 0.4th centile)\r\nAND at least one of:\r\n- History of small for gestational age (birth weight and/or length <-2SDS)\r\n- Body disproportion, e.g. discrepancy between stature and head size\r\n- Dysmorphic features and congenital anomalies\r\n- Abnormalities in the GH-IGF axis (evidence of GH insensitivity or deficiency) and/or other pituitary hormonal deficiencies\r\n- Family history of significant short stature (1st and 2nd degree relatives) and/or consanguinity\r\n\r\nPrior to genomic testing consider:\r\n-Chromosomal microarray analysis (e.g. Turner syndrome)\r\n-Methylation analysis for Russell-Silver syndrome and Temple syndrome\r\n-Skeletal survey\r\n\r\nAcquired causes of short stature are relatively common.\r\n\r\nDepending on the specific clinical features present, consider applying the Skeletal dysplasia, Intellectual Disability, and/or Pituitary Hormone deficiency panels.\r\n\r\nWith thanks to Genomics England for the original design of this panel.",
                "status": "public",
                "version": "1.102",
                "version_created": "2026-04-01T10:17:12.005431+11:00",
                "relevant_disorders": [
                    "Failure to thrive",
                    "HP:0001508; Growth delay",
                    "HP:0001510"
                ],
                "stats": {
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                    "number_of_strs": 0,
                    "number_of_regions": 4
                },
                "types": [
                    {
                        "name": "Victorian Clinical Genetics Services",
                        "slug": "victorian-clinical-genetics-services",
                        "description": "Panel used by VCGS."
                    },
                    {
                        "name": "Genetic Health Queensland",
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                        "description": "Panel used by GHQ."
                    },
                    {
                        "name": "Royal Melbourne Hospital",
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                    },
                    {
                        "name": "Rare Disease",
                        "slug": "rare-disease",
                        "description": "Rare disease panels"
                    }
                ],
                "child_panel_ids": []
            },
            "transcript": []
        },
        {
            "gene_data": {
                "alias": [
                    "FLJ38144",
                    "hang"
                ],
                "biotype": "protein_coding",
                "hgnc_id": "HGNC:24750",
                "gene_name": "zinc finger protein 699",
                "omim_gene": [
                    "609571"
                ],
                "alias_name": null,
                "gene_symbol": "ZNF699",
                "hgnc_symbol": "ZNF699",
                "hgnc_release": "2017-11-03",
                "ensembl_genes": {
                    "GRch37": {
                        "82": {
                            "location": "19:9404951-9420514",
                            "ensembl_id": "ENSG00000196110"
                        }
                    },
                    "GRch38": {
                        "90": {
                            "location": "19:9294275-9309838",
                            "ensembl_id": "ENSG00000196110"
                        }
                    }
                },
                "hgnc_date_symbol_changed": "2005-08-11"
            },
            "entity_type": "gene",
            "entity_name": "ZNF699",
            "confidence_level": "3",
            "penetrance": null,
            "mode_of_pathogenicity": null,
            "publications": [
                "33875846"
            ],
            "evidence": [
                "Expert Review Green",
                "Literature"
            ],
            "phenotypes": [
                "DEGCAGS syndrome, MIM# 619488"
            ],
            "mode_of_inheritance": "BIALLELIC, autosomal or pseudoautosomal",
            "tags": [],
            "panel": {
                "id": 3631,
                "hash_id": null,
                "name": "Growth failure",
                "disease_group": "",
                "disease_sub_group": "",
                "description": "This panel contains genes associated with growth failure in infancy/early childhood, either isolated or as part of another disorder.\r\n\r\nConsider applying this panel in individuals with:\r\n -Height Standard Deviation Score (SDS) <-3 (very significant short stature - well below the 0.4th centile)\r\nAND at least one of:\r\n- History of small for gestational age (birth weight and/or length <-2SDS)\r\n- Body disproportion, e.g. discrepancy between stature and head size\r\n- Dysmorphic features and congenital anomalies\r\n- Abnormalities in the GH-IGF axis (evidence of GH insensitivity or deficiency) and/or other pituitary hormonal deficiencies\r\n- Family history of significant short stature (1st and 2nd degree relatives) and/or consanguinity\r\n\r\nPrior to genomic testing consider:\r\n-Chromosomal microarray analysis (e.g. Turner syndrome)\r\n-Methylation analysis for Russell-Silver syndrome and Temple syndrome\r\n-Skeletal survey\r\n\r\nAcquired causes of short stature are relatively common.\r\n\r\nDepending on the specific clinical features present, consider applying the Skeletal dysplasia, Intellectual Disability, and/or Pituitary Hormone deficiency panels.\r\n\r\nWith thanks to Genomics England for the original design of this panel.",
                "status": "public",
                "version": "1.102",
                "version_created": "2026-04-01T10:17:12.005431+11:00",
                "relevant_disorders": [
                    "Failure to thrive",
                    "HP:0001508; Growth delay",
                    "HP:0001510"
                ],
                "stats": {
                    "number_of_genes": 204,
                    "number_of_strs": 0,
                    "number_of_regions": 4
                },
                "types": [
                    {
                        "name": "Victorian Clinical Genetics Services",
                        "slug": "victorian-clinical-genetics-services",
                        "description": "Panel used by VCGS."
                    },
                    {
                        "name": "Genetic Health Queensland",
                        "slug": "genetic-health-queensland",
                        "description": "Panel used by GHQ."
                    },
                    {
                        "name": "Royal Melbourne Hospital",
                        "slug": "royal-melbourne-hospital",
                        "description": "Royal Melbourne Hospital"
                    },
                    {
                        "name": "Rare Disease",
                        "slug": "rare-disease",
                        "description": "Rare disease panels"
                    }
                ],
                "child_panel_ids": []
            },
            "transcript": []
        },
        {
            "gene_data": {
                "alias": [
                    "LZTR-1",
                    "BTBD29"
                ],
                "biotype": "protein_coding",
                "hgnc_id": "HGNC:6742",
                "gene_name": "leucine zipper like transcription regulator 1",
                "omim_gene": [
                    "600574"
                ],
                "alias_name": null,
                "gene_symbol": "LZTR1",
                "hgnc_symbol": "LZTR1",
                "hgnc_release": "2017-11-03",
                "ensembl_genes": {
                    "GRch37": {
                        "82": {
                            "location": "22:21333751-21353327",
                            "ensembl_id": "ENSG00000099949"
                        }
                    },
                    "GRch38": {
                        "90": {
                            "location": "22:20979462-20999038",
                            "ensembl_id": "ENSG00000099949"
                        }
                    }
                },
                "hgnc_date_symbol_changed": "1999-10-19"
            },
            "entity_type": "gene",
            "entity_name": "LZTR1",
            "confidence_level": "3",
            "penetrance": null,
            "mode_of_pathogenicity": "",
            "publications": [
                "25795793",
                "29469822",
                "30368668",
                "30481304",
                "24362817"
            ],
            "evidence": [
                "Expert Review Green",
                "Genomics England PanelApp",
                "Victorian Clinical Genetics Services"
            ],
            "phenotypes": [
                "Noonan syndrome 10",
                "Noonan syndrome 2"
            ],
            "mode_of_inheritance": "BOTH monoallelic and biallelic, autosomal or pseudoautosomal",
            "tags": [],
            "panel": {
                "id": 3631,
                "hash_id": null,
                "name": "Growth failure",
                "disease_group": "",
                "disease_sub_group": "",
                "description": "This panel contains genes associated with growth failure in infancy/early childhood, either isolated or as part of another disorder.\r\n\r\nConsider applying this panel in individuals with:\r\n -Height Standard Deviation Score (SDS) <-3 (very significant short stature - well below the 0.4th centile)\r\nAND at least one of:\r\n- History of small for gestational age (birth weight and/or length <-2SDS)\r\n- Body disproportion, e.g. discrepancy between stature and head size\r\n- Dysmorphic features and congenital anomalies\r\n- Abnormalities in the GH-IGF axis (evidence of GH insensitivity or deficiency) and/or other pituitary hormonal deficiencies\r\n- Family history of significant short stature (1st and 2nd degree relatives) and/or consanguinity\r\n\r\nPrior to genomic testing consider:\r\n-Chromosomal microarray analysis (e.g. Turner syndrome)\r\n-Methylation analysis for Russell-Silver syndrome and Temple syndrome\r\n-Skeletal survey\r\n\r\nAcquired causes of short stature are relatively common.\r\n\r\nDepending on the specific clinical features present, consider applying the Skeletal dysplasia, Intellectual Disability, and/or Pituitary Hormone deficiency panels.\r\n\r\nWith thanks to Genomics England for the original design of this panel.",
                "status": "public",
                "version": "1.102",
                "version_created": "2026-04-01T10:17:12.005431+11:00",
                "relevant_disorders": [
                    "Failure to thrive",
                    "HP:0001508; Growth delay",
                    "HP:0001510"
                ],
                "stats": {
                    "number_of_genes": 204,
                    "number_of_strs": 0,
                    "number_of_regions": 4
                },
                "types": [
                    {
                        "name": "Victorian Clinical Genetics Services",
                        "slug": "victorian-clinical-genetics-services",
                        "description": "Panel used by VCGS."
                    },
                    {
                        "name": "Genetic Health Queensland",
                        "slug": "genetic-health-queensland",
                        "description": "Panel used by GHQ."
                    },
                    {
                        "name": "Royal Melbourne Hospital",
                        "slug": "royal-melbourne-hospital",
                        "description": "Royal Melbourne Hospital"
                    },
                    {
                        "name": "Rare Disease",
                        "slug": "rare-disease",
                        "description": "Rare disease panels"
                    }
                ],
                "child_panel_ids": []
            },
            "transcript": null
        },
        {
            "gene_data": {
                "alias": [
                    "MEK1",
                    "MAPKK1"
                ],
                "biotype": "protein_coding",
                "hgnc_id": "HGNC:6840",
                "gene_name": "mitogen-activated protein kinase kinase 1",
                "omim_gene": [
                    "176872"
                ],
                "alias_name": null,
                "gene_symbol": "MAP2K1",
                "hgnc_symbol": "MAP2K1",
                "hgnc_release": "2017-11-03",
                "ensembl_genes": {
                    "GRch37": {
                        "82": {
                            "location": "15:66679155-66784650",
                            "ensembl_id": "ENSG00000169032"
                        }
                    },
                    "GRch38": {
                        "90": {
                            "location": "15:66386817-66492312",
                            "ensembl_id": "ENSG00000169032"
                        }
                    }
                },
                "hgnc_date_symbol_changed": "1993-11-05"
            },
            "entity_type": "gene",
            "entity_name": "MAP2K1",
            "confidence_level": "3",
            "penetrance": null,
            "mode_of_pathogenicity": "Loss-of-function variants (as defined in pop up message) DO NOT cause this phenotype - please provide details in the comments",
            "publications": [
                "23321623",
                "16439621",
                "21396583",
                "16825433",
                "17551924",
                "18042262",
                "20301365"
            ],
            "evidence": [
                "Expert Review Green",
                "Genomics England PanelApp",
                "Victorian Clinical Genetics Services"
            ],
            "phenotypes": [
                "Cardiofaciocutaneous syndrome 3, MIM# 615279"
            ],
            "mode_of_inheritance": "MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted",
            "tags": [],
            "panel": {
                "id": 3631,
                "hash_id": null,
                "name": "Growth failure",
                "disease_group": "",
                "disease_sub_group": "",
                "description": "This panel contains genes associated with growth failure in infancy/early childhood, either isolated or as part of another disorder.\r\n\r\nConsider applying this panel in individuals with:\r\n -Height Standard Deviation Score (SDS) <-3 (very significant short stature - well below the 0.4th centile)\r\nAND at least one of:\r\n- History of small for gestational age (birth weight and/or length <-2SDS)\r\n- Body disproportion, e.g. discrepancy between stature and head size\r\n- Dysmorphic features and congenital anomalies\r\n- Abnormalities in the GH-IGF axis (evidence of GH insensitivity or deficiency) and/or other pituitary hormonal deficiencies\r\n- Family history of significant short stature (1st and 2nd degree relatives) and/or consanguinity\r\n\r\nPrior to genomic testing consider:\r\n-Chromosomal microarray analysis (e.g. Turner syndrome)\r\n-Methylation analysis for Russell-Silver syndrome and Temple syndrome\r\n-Skeletal survey\r\n\r\nAcquired causes of short stature are relatively common.\r\n\r\nDepending on the specific clinical features present, consider applying the Skeletal dysplasia, Intellectual Disability, and/or Pituitary Hormone deficiency panels.\r\n\r\nWith thanks to Genomics England for the original design of this panel.",
                "status": "public",
                "version": "1.102",
                "version_created": "2026-04-01T10:17:12.005431+11:00",
                "relevant_disorders": [
                    "Failure to thrive",
                    "HP:0001508; Growth delay",
                    "HP:0001510"
                ],
                "stats": {
                    "number_of_genes": 204,
                    "number_of_strs": 0,
                    "number_of_regions": 4
                },
                "types": [
                    {
                        "name": "Victorian Clinical Genetics Services",
                        "slug": "victorian-clinical-genetics-services",
                        "description": "Panel used by VCGS."
                    },
                    {
                        "name": "Genetic Health Queensland",
                        "slug": "genetic-health-queensland",
                        "description": "Panel used by GHQ."
                    },
                    {
                        "name": "Royal Melbourne Hospital",
                        "slug": "royal-melbourne-hospital",
                        "description": "Royal Melbourne Hospital"
                    },
                    {
                        "name": "Rare Disease",
                        "slug": "rare-disease",
                        "description": "Rare disease panels"
                    }
                ],
                "child_panel_ids": []
            },
            "transcript": null
        },
        {
            "gene_data": {
                "alias": [
                    "MEK2"
                ],
                "biotype": "protein_coding",
                "hgnc_id": "HGNC:6842",
                "gene_name": "mitogen-activated protein kinase kinase 2",
                "omim_gene": [
                    "601263"
                ],
                "alias_name": null,
                "gene_symbol": "MAP2K2",
                "hgnc_symbol": "MAP2K2",
                "hgnc_release": "2017-11-03",
                "ensembl_genes": {
                    "GRch37": {
                        "82": {
                            "location": "19:4090319-4124126",
                            "ensembl_id": "ENSG00000126934"
                        }
                    },
                    "GRch38": {
                        "90": {
                            "location": "19:4090321-4124129",
                            "ensembl_id": "ENSG00000126934"
                        }
                    }
                },
                "hgnc_date_symbol_changed": "1993-11-05"
            },
            "entity_type": "gene",
            "entity_name": "MAP2K2",
            "confidence_level": "3",
            "penetrance": null,
            "mode_of_pathogenicity": "Loss-of-function variants (as defined in pop up message) DO NOT cause this phenotype - please provide details in the comments",
            "publications": [
                "16439621",
                "21396583",
                "23379592",
                "20358587",
                "16439621",
                "18042262"
            ],
            "evidence": [
                "Expert Review Green",
                "Genomics England PanelApp",
                "Victorian Clinical Genetics Services"
            ],
            "phenotypes": [
                "Cardiofaciocutaneous syndrome 4, MIM# 615280"
            ],
            "mode_of_inheritance": "MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted",
            "tags": [],
            "panel": {
                "id": 3631,
                "hash_id": null,
                "name": "Growth failure",
                "disease_group": "",
                "disease_sub_group": "",
                "description": "This panel contains genes associated with growth failure in infancy/early childhood, either isolated or as part of another disorder.\r\n\r\nConsider applying this panel in individuals with:\r\n -Height Standard Deviation Score (SDS) <-3 (very significant short stature - well below the 0.4th centile)\r\nAND at least one of:\r\n- History of small for gestational age (birth weight and/or length <-2SDS)\r\n- Body disproportion, e.g. discrepancy between stature and head size\r\n- Dysmorphic features and congenital anomalies\r\n- Abnormalities in the GH-IGF axis (evidence of GH insensitivity or deficiency) and/or other pituitary hormonal deficiencies\r\n- Family history of significant short stature (1st and 2nd degree relatives) and/or consanguinity\r\n\r\nPrior to genomic testing consider:\r\n-Chromosomal microarray analysis (e.g. Turner syndrome)\r\n-Methylation analysis for Russell-Silver syndrome and Temple syndrome\r\n-Skeletal survey\r\n\r\nAcquired causes of short stature are relatively common.\r\n\r\nDepending on the specific clinical features present, consider applying the Skeletal dysplasia, Intellectual Disability, and/or Pituitary Hormone deficiency panels.\r\n\r\nWith thanks to Genomics England for the original design of this panel.",
                "status": "public",
                "version": "1.102",
                "version_created": "2026-04-01T10:17:12.005431+11:00",
                "relevant_disorders": [
                    "Failure to thrive",
                    "HP:0001508; Growth delay",
                    "HP:0001510"
                ],
                "stats": {
                    "number_of_genes": 204,
                    "number_of_strs": 0,
                    "number_of_regions": 4
                },
                "types": [
                    {
                        "name": "Victorian Clinical Genetics Services",
                        "slug": "victorian-clinical-genetics-services",
                        "description": "Panel used by VCGS."
                    },
                    {
                        "name": "Genetic Health Queensland",
                        "slug": "genetic-health-queensland",
                        "description": "Panel used by GHQ."
                    },
                    {
                        "name": "Royal Melbourne Hospital",
                        "slug": "royal-melbourne-hospital",
                        "description": "Royal Melbourne Hospital"
                    },
                    {
                        "name": "Rare Disease",
                        "slug": "rare-disease",
                        "description": "Rare disease panels"
                    }
                ],
                "child_panel_ids": []
            },
            "transcript": null
        },
        {
            "gene_data": {
                "alias": [
                    "ATV",
                    "AT-V2",
                    "AT-V1"
                ],
                "biotype": "protein_coding",
                "hgnc_id": "HGNC:7652",
                "gene_name": "nibrin",
                "omim_gene": [
                    "602667"
                ],
                "alias_name": null,
                "gene_symbol": "NBN",
                "hgnc_symbol": "NBN",
                "hgnc_release": "2017-11-03",
                "ensembl_genes": {
                    "GRch37": {
                        "82": {
                            "location": "8:90945564-91015456",
                            "ensembl_id": "ENSG00000104320"
                        }
                    },
                    "GRch38": {
                        "90": {
                            "location": "8:89933336-90003228",
                            "ensembl_id": "ENSG00000104320"
                        }
                    }
                },
                "hgnc_date_symbol_changed": "2005-06-02"
            },
            "entity_type": "gene",
            "entity_name": "NBN",
            "confidence_level": "3",
            "penetrance": null,
            "mode_of_pathogenicity": "",
            "publications": [
                "33488600",
                "33082212"
            ],
            "evidence": [
                "Expert Review Green",
                "Genomics England PanelApp",
                "Victorian Clinical Genetics Services"
            ],
            "phenotypes": [
                "Nijmegen breakage syndrome, MIM# 251260",
                "MONDO:0009623"
            ],
            "mode_of_inheritance": "BIALLELIC, autosomal or pseudoautosomal",
            "tags": [],
            "panel": {
                "id": 3631,
                "hash_id": null,
                "name": "Growth failure",
                "disease_group": "",
                "disease_sub_group": "",
                "description": "This panel contains genes associated with growth failure in infancy/early childhood, either isolated or as part of another disorder.\r\n\r\nConsider applying this panel in individuals with:\r\n -Height Standard Deviation Score (SDS) <-3 (very significant short stature - well below the 0.4th centile)\r\nAND at least one of:\r\n- History of small for gestational age (birth weight and/or length <-2SDS)\r\n- Body disproportion, e.g. discrepancy between stature and head size\r\n- Dysmorphic features and congenital anomalies\r\n- Abnormalities in the GH-IGF axis (evidence of GH insensitivity or deficiency) and/or other pituitary hormonal deficiencies\r\n- Family history of significant short stature (1st and 2nd degree relatives) and/or consanguinity\r\n\r\nPrior to genomic testing consider:\r\n-Chromosomal microarray analysis (e.g. Turner syndrome)\r\n-Methylation analysis for Russell-Silver syndrome and Temple syndrome\r\n-Skeletal survey\r\n\r\nAcquired causes of short stature are relatively common.\r\n\r\nDepending on the specific clinical features present, consider applying the Skeletal dysplasia, Intellectual Disability, and/or Pituitary Hormone deficiency panels.\r\n\r\nWith thanks to Genomics England for the original design of this panel.",
                "status": "public",
                "version": "1.102",
                "version_created": "2026-04-01T10:17:12.005431+11:00",
                "relevant_disorders": [
                    "Failure to thrive",
                    "HP:0001508; Growth delay",
                    "HP:0001510"
                ],
                "stats": {
                    "number_of_genes": 204,
                    "number_of_strs": 0,
                    "number_of_regions": 4
                },
                "types": [
                    {
                        "name": "Victorian Clinical Genetics Services",
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                        "description": "Panel used by VCGS."
                    },
                    {
                        "name": "Genetic Health Queensland",
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                    {
                        "name": "Royal Melbourne Hospital",
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                    {
                        "name": "Rare Disease",
                        "slug": "rare-disease",
                        "description": "Rare disease panels"
                    }
                ],
                "child_panel_ids": []
            },
            "transcript": null
        },
        {
            "gene_data": {
                "alias": [
                    "N-ras"
                ],
                "biotype": "protein_coding",
                "hgnc_id": "HGNC:7989",
                "gene_name": "NRAS proto-oncogene, GTPase",
                "omim_gene": [
                    "164790"
                ],
                "alias_name": null,
                "gene_symbol": "NRAS",
                "hgnc_symbol": "NRAS",
                "hgnc_release": "2017-11-03",
                "ensembl_genes": {
                    "GRch37": {
                        "82": {
                            "location": "1:115247090-115259515",
                            "ensembl_id": "ENSG00000213281"
                        }
                    },
                    "GRch38": {
                        "90": {
                            "location": "1:114704469-114716894",
                            "ensembl_id": "ENSG00000213281"
                        }
                    }
                },
                "hgnc_date_symbol_changed": "2001-06-22"
            },
            "entity_type": "gene",
            "entity_name": "NRAS",
            "confidence_level": "3",
            "penetrance": null,
            "mode_of_pathogenicity": "Loss-of-function variants (as defined in pop up message) DO NOT cause this phenotype - please provide details in the comments",
            "publications": [
                "19966803",
                "19775298",
                "26467218",
                "28594414"
            ],
            "evidence": [
                "Expert Review Green",
                "Genomics England PanelApp",
                "Victorian Clinical Genetics Services"
            ],
            "phenotypes": [
                "Noonan syndrome 6, MIM# 613224"
            ],
            "mode_of_inheritance": "MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted",
            "tags": [],
            "panel": {
                "id": 3631,
                "hash_id": null,
                "name": "Growth failure",
                "disease_group": "",
                "disease_sub_group": "",
                "description": "This panel contains genes associated with growth failure in infancy/early childhood, either isolated or as part of another disorder.\r\n\r\nConsider applying this panel in individuals with:\r\n -Height Standard Deviation Score (SDS) <-3 (very significant short stature - well below the 0.4th centile)\r\nAND at least one of:\r\n- History of small for gestational age (birth weight and/or length <-2SDS)\r\n- Body disproportion, e.g. discrepancy between stature and head size\r\n- Dysmorphic features and congenital anomalies\r\n- Abnormalities in the GH-IGF axis (evidence of GH insensitivity or deficiency) and/or other pituitary hormonal deficiencies\r\n- Family history of significant short stature (1st and 2nd degree relatives) and/or consanguinity\r\n\r\nPrior to genomic testing consider:\r\n-Chromosomal microarray analysis (e.g. Turner syndrome)\r\n-Methylation analysis for Russell-Silver syndrome and Temple syndrome\r\n-Skeletal survey\r\n\r\nAcquired causes of short stature are relatively common.\r\n\r\nDepending on the specific clinical features present, consider applying the Skeletal dysplasia, Intellectual Disability, and/or Pituitary Hormone deficiency panels.\r\n\r\nWith thanks to Genomics England for the original design of this panel.",
                "status": "public",
                "version": "1.102",
                "version_created": "2026-04-01T10:17:12.005431+11:00",
                "relevant_disorders": [
                    "Failure to thrive",
                    "HP:0001508; Growth delay",
                    "HP:0001510"
                ],
                "stats": {
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                    "number_of_strs": 0,
                    "number_of_regions": 4
                },
                "types": [
                    {
                        "name": "Victorian Clinical Genetics Services",
                        "slug": "victorian-clinical-genetics-services",
                        "description": "Panel used by VCGS."
                    },
                    {
                        "name": "Genetic Health Queensland",
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                    },
                    {
                        "name": "Royal Melbourne Hospital",
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                    },
                    {
                        "name": "Rare Disease",
                        "slug": "rare-disease",
                        "description": "Rare disease panels"
                    }
                ],
                "child_panel_ids": []
            },
            "transcript": null
        },
        {
            "gene_data": {
                "alias": [
                    "KIAA0657"
                ],
                "biotype": "protein_coding",
                "hgnc_id": "HGNC:29092",
                "gene_name": "obscurin like 1",
                "omim_gene": [
                    "610991"
                ],
                "alias_name": null,
                "gene_symbol": "OBSL1",
                "hgnc_symbol": "OBSL1",
                "hgnc_release": "2017-11-03",
                "ensembl_genes": {
                    "GRch37": {
                        "82": {
                            "location": "2:220415451-220436581",
                            "ensembl_id": "ENSG00000124006"
                        }
                    },
                    "GRch38": {
                        "90": {
                            "location": "2:219550729-219571859",
                            "ensembl_id": "ENSG00000124006"
                        }
                    }
                },
                "hgnc_date_symbol_changed": "2005-10-20"
            },
            "entity_type": "gene",
            "entity_name": "OBSL1",
            "confidence_level": "3",
            "penetrance": null,
            "mode_of_pathogenicity": "",
            "publications": [
                "21737058",
                "19481195",
                "23018678",
                "19877176"
            ],
            "evidence": [
                "Expert Review Green",
                "Genomics England PanelApp"
            ],
            "phenotypes": [
                "3-M syndrome 2, MIM #612921"
            ],
            "mode_of_inheritance": "BIALLELIC, autosomal or pseudoautosomal",
            "tags": [],
            "panel": {
                "id": 3631,
                "hash_id": null,
                "name": "Growth failure",
                "disease_group": "",
                "disease_sub_group": "",
                "description": "This panel contains genes associated with growth failure in infancy/early childhood, either isolated or as part of another disorder.\r\n\r\nConsider applying this panel in individuals with:\r\n -Height Standard Deviation Score (SDS) <-3 (very significant short stature - well below the 0.4th centile)\r\nAND at least one of:\r\n- History of small for gestational age (birth weight and/or length <-2SDS)\r\n- Body disproportion, e.g. discrepancy between stature and head size\r\n- Dysmorphic features and congenital anomalies\r\n- Abnormalities in the GH-IGF axis (evidence of GH insensitivity or deficiency) and/or other pituitary hormonal deficiencies\r\n- Family history of significant short stature (1st and 2nd degree relatives) and/or consanguinity\r\n\r\nPrior to genomic testing consider:\r\n-Chromosomal microarray analysis (e.g. Turner syndrome)\r\n-Methylation analysis for Russell-Silver syndrome and Temple syndrome\r\n-Skeletal survey\r\n\r\nAcquired causes of short stature are relatively common.\r\n\r\nDepending on the specific clinical features present, consider applying the Skeletal dysplasia, Intellectual Disability, and/or Pituitary Hormone deficiency panels.\r\n\r\nWith thanks to Genomics England for the original design of this panel.",
                "status": "public",
                "version": "1.102",
                "version_created": "2026-04-01T10:17:12.005431+11:00",
                "relevant_disorders": [
                    "Failure to thrive",
                    "HP:0001508; Growth delay",
                    "HP:0001510"
                ],
                "stats": {
                    "number_of_genes": 204,
                    "number_of_strs": 0,
                    "number_of_regions": 4
                },
                "types": [
                    {
                        "name": "Victorian Clinical Genetics Services",
                        "slug": "victorian-clinical-genetics-services",
                        "description": "Panel used by VCGS."
                    },
                    {
                        "name": "Genetic Health Queensland",
                        "slug": "genetic-health-queensland",
                        "description": "Panel used by GHQ."
                    },
                    {
                        "name": "Royal Melbourne Hospital",
                        "slug": "royal-melbourne-hospital",
                        "description": "Royal Melbourne Hospital"
                    },
                    {
                        "name": "Rare Disease",
                        "slug": "rare-disease",
                        "description": "Rare disease panels"
                    }
                ],
                "child_panel_ids": []
            },
            "transcript": null
        },
        {
            "gene_data": {
                "alias": [
                    "FLJ21816",
                    "FANCN"
                ],
                "biotype": "protein_coding",
                "hgnc_id": "HGNC:26144",
                "gene_name": "partner and localizer of BRCA2",
                "omim_gene": [
                    "610355"
                ],
                "alias_name": [
                    "Fanconi anemia, complementation group N"
                ],
                "gene_symbol": "PALB2",
                "hgnc_symbol": "PALB2",
                "hgnc_release": "2017-11-03",
                "ensembl_genes": {
                    "GRch37": {
                        "82": {
                            "location": "16:23614488-23652631",
                            "ensembl_id": "ENSG00000083093"
                        }
                    },
                    "GRch38": {
                        "90": {
                            "location": "16:23603160-23641310",
                            "ensembl_id": "ENSG00000083093"
                        }
                    }
                },
                "hgnc_date_symbol_changed": "2007-01-15"
            },
            "entity_type": "gene",
            "entity_name": "PALB2",
            "confidence_level": "3",
            "penetrance": null,
            "mode_of_pathogenicity": "",
            "publications": [
                "17200672",
                "17200671"
            ],
            "evidence": [
                "Expert Review Green",
                "Genomics England PanelApp",
                "Victorian Clinical Genetics Services"
            ],
            "phenotypes": [
                "Fanconi anaemia, complementation group N, MIM# 610832"
            ],
            "mode_of_inheritance": "BIALLELIC, autosomal or pseudoautosomal",
            "tags": [],
            "panel": {
                "id": 3631,
                "hash_id": null,
                "name": "Growth failure",
                "disease_group": "",
                "disease_sub_group": "",
                "description": "This panel contains genes associated with growth failure in infancy/early childhood, either isolated or as part of another disorder.\r\n\r\nConsider applying this panel in individuals with:\r\n -Height Standard Deviation Score (SDS) <-3 (very significant short stature - well below the 0.4th centile)\r\nAND at least one of:\r\n- History of small for gestational age (birth weight and/or length <-2SDS)\r\n- Body disproportion, e.g. discrepancy between stature and head size\r\n- Dysmorphic features and congenital anomalies\r\n- Abnormalities in the GH-IGF axis (evidence of GH insensitivity or deficiency) and/or other pituitary hormonal deficiencies\r\n- Family history of significant short stature (1st and 2nd degree relatives) and/or consanguinity\r\n\r\nPrior to genomic testing consider:\r\n-Chromosomal microarray analysis (e.g. Turner syndrome)\r\n-Methylation analysis for Russell-Silver syndrome and Temple syndrome\r\n-Skeletal survey\r\n\r\nAcquired causes of short stature are relatively common.\r\n\r\nDepending on the specific clinical features present, consider applying the Skeletal dysplasia, Intellectual Disability, and/or Pituitary Hormone deficiency panels.\r\n\r\nWith thanks to Genomics England for the original design of this panel.",
                "status": "public",
                "version": "1.102",
                "version_created": "2026-04-01T10:17:12.005431+11:00",
                "relevant_disorders": [
                    "Failure to thrive",
                    "HP:0001508; Growth delay",
                    "HP:0001510"
                ],
                "stats": {
                    "number_of_genes": 204,
                    "number_of_strs": 0,
                    "number_of_regions": 4
                },
                "types": [
                    {
                        "name": "Victorian Clinical Genetics Services",
                        "slug": "victorian-clinical-genetics-services",
                        "description": "Panel used by VCGS."
                    },
                    {
                        "name": "Genetic Health Queensland",
                        "slug": "genetic-health-queensland",
                        "description": "Panel used by GHQ."
                    },
                    {
                        "name": "Royal Melbourne Hospital",
                        "slug": "royal-melbourne-hospital",
                        "description": "Royal Melbourne Hospital"
                    },
                    {
                        "name": "Rare Disease",
                        "slug": "rare-disease",
                        "description": "Rare disease panels"
                    }
                ],
                "child_panel_ids": []
            },
            "transcript": null
        },
        {
            "gene_data": {
                "alias": [
                    "GRB1",
                    "p85-ALPHA",
                    "p85"
                ],
                "biotype": "protein_coding",
                "hgnc_id": "HGNC:8979",
                "gene_name": "phosphoinositide-3-kinase regulatory subunit 1",
                "omim_gene": [
                    "171833"
                ],
                "alias_name": [
                    "phosphoinositide-3-kinase regulatory subunit alpha"
                ],
                "gene_symbol": "PIK3R1",
                "hgnc_symbol": "PIK3R1",
                "hgnc_release": "2017-11-03",
                "ensembl_genes": {
                    "GRch37": {
                        "82": {
                            "location": "5:67511548-67597649",
                            "ensembl_id": "ENSG00000145675"
                        }
                    },
                    "GRch38": {
                        "90": {
                            "location": "5:68215720-68301821",
                            "ensembl_id": "ENSG00000145675"
                        }
                    }
                },
                "hgnc_date_symbol_changed": "1992-12-08"
            },
            "entity_type": "gene",
            "entity_name": "PIK3R1",
            "confidence_level": "3",
            "penetrance": null,
            "mode_of_pathogenicity": "",
            "publications": [
                "23810378",
                "23810379",
                "23810382"
            ],
            "evidence": [
                "Expert Review Green",
                "Genomics England PanelApp"
            ],
            "phenotypes": [
                "SHORT syndrome, OMIM # 269880"
            ],
            "mode_of_inheritance": "MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted",
            "tags": [],
            "panel": {
                "id": 3631,
                "hash_id": null,
                "name": "Growth failure",
                "disease_group": "",
                "disease_sub_group": "",
                "description": "This panel contains genes associated with growth failure in infancy/early childhood, either isolated or as part of another disorder.\r\n\r\nConsider applying this panel in individuals with:\r\n -Height Standard Deviation Score (SDS) <-3 (very significant short stature - well below the 0.4th centile)\r\nAND at least one of:\r\n- History of small for gestational age (birth weight and/or length <-2SDS)\r\n- Body disproportion, e.g. discrepancy between stature and head size\r\n- Dysmorphic features and congenital anomalies\r\n- Abnormalities in the GH-IGF axis (evidence of GH insensitivity or deficiency) and/or other pituitary hormonal deficiencies\r\n- Family history of significant short stature (1st and 2nd degree relatives) and/or consanguinity\r\n\r\nPrior to genomic testing consider:\r\n-Chromosomal microarray analysis (e.g. Turner syndrome)\r\n-Methylation analysis for Russell-Silver syndrome and Temple syndrome\r\n-Skeletal survey\r\n\r\nAcquired causes of short stature are relatively common.\r\n\r\nDepending on the specific clinical features present, consider applying the Skeletal dysplasia, Intellectual Disability, and/or Pituitary Hormone deficiency panels.\r\n\r\nWith thanks to Genomics England for the original design of this panel.",
                "status": "public",
                "version": "1.102",
                "version_created": "2026-04-01T10:17:12.005431+11:00",
                "relevant_disorders": [
                    "Failure to thrive",
                    "HP:0001508; Growth delay",
                    "HP:0001510"
                ],
                "stats": {
                    "number_of_genes": 204,
                    "number_of_strs": 0,
                    "number_of_regions": 4
                },
                "types": [
                    {
                        "name": "Victorian Clinical Genetics Services",
                        "slug": "victorian-clinical-genetics-services",
                        "description": "Panel used by VCGS."
                    },
                    {
                        "name": "Genetic Health Queensland",
                        "slug": "genetic-health-queensland",
                        "description": "Panel used by GHQ."
                    },
                    {
                        "name": "Royal Melbourne Hospital",
                        "slug": "royal-melbourne-hospital",
                        "description": "Royal Melbourne Hospital"
                    },
                    {
                        "name": "Rare Disease",
                        "slug": "rare-disease",
                        "description": "Rare disease panels"
                    }
                ],
                "child_panel_ids": []
            },
            "transcript": null
        },
        {
            "gene_data": {
                "alias": [
                    "ZNF912"
                ],
                "biotype": "protein_coding",
                "hgnc_id": "HGNC:9045",
                "gene_name": "PLAG1 zinc finger",
                "omim_gene": [
                    "603026"
                ],
                "alias_name": null,
                "gene_symbol": "PLAG1",
                "hgnc_symbol": "PLAG1",
                "hgnc_release": "2017-11-03",
                "ensembl_genes": {
                    "GRch37": {
                        "82": {
                            "location": "8:57073463-57123883",
                            "ensembl_id": "ENSG00000181690"
                        }
                    },
                    "GRch38": {
                        "90": {
                            "location": "8:56160904-56211324",
                            "ensembl_id": "ENSG00000181690"
                        }
                    }
                },
                "hgnc_date_symbol_changed": "1998-02-11"
            },
            "entity_type": "gene",
            "entity_name": "PLAG1",
            "confidence_level": "3",
            "penetrance": null,
            "mode_of_pathogenicity": "",
            "publications": [
                "28796236",
                "33291420",
                "32546215"
            ],
            "evidence": [
                "Expert Review Green",
                "Genomics England PanelApp"
            ],
            "phenotypes": [
                "Silver-Russell syndrome 4, MIM # 618907"
            ],
            "mode_of_inheritance": "MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted",
            "tags": [],
            "panel": {
                "id": 3631,
                "hash_id": null,
                "name": "Growth failure",
                "disease_group": "",
                "disease_sub_group": "",
                "description": "This panel contains genes associated with growth failure in infancy/early childhood, either isolated or as part of another disorder.\r\n\r\nConsider applying this panel in individuals with:\r\n -Height Standard Deviation Score (SDS) <-3 (very significant short stature - well below the 0.4th centile)\r\nAND at least one of:\r\n- History of small for gestational age (birth weight and/or length <-2SDS)\r\n- Body disproportion, e.g. discrepancy between stature and head size\r\n- Dysmorphic features and congenital anomalies\r\n- Abnormalities in the GH-IGF axis (evidence of GH insensitivity or deficiency) and/or other pituitary hormonal deficiencies\r\n- Family history of significant short stature (1st and 2nd degree relatives) and/or consanguinity\r\n\r\nPrior to genomic testing consider:\r\n-Chromosomal microarray analysis (e.g. Turner syndrome)\r\n-Methylation analysis for Russell-Silver syndrome and Temple syndrome\r\n-Skeletal survey\r\n\r\nAcquired causes of short stature are relatively common.\r\n\r\nDepending on the specific clinical features present, consider applying the Skeletal dysplasia, Intellectual Disability, and/or Pituitary Hormone deficiency panels.\r\n\r\nWith thanks to Genomics England for the original design of this panel.",
                "status": "public",
                "version": "1.102",
                "version_created": "2026-04-01T10:17:12.005431+11:00",
                "relevant_disorders": [
                    "Failure to thrive",
                    "HP:0001508; Growth delay",
                    "HP:0001510"
                ],
                "stats": {
                    "number_of_genes": 204,
                    "number_of_strs": 0,
                    "number_of_regions": 4
                },
                "types": [
                    {
                        "name": "Victorian Clinical Genetics Services",
                        "slug": "victorian-clinical-genetics-services",
                        "description": "Panel used by VCGS."
                    },
                    {
                        "name": "Genetic Health Queensland",
                        "slug": "genetic-health-queensland",
                        "description": "Panel used by GHQ."
                    },
                    {
                        "name": "Royal Melbourne Hospital",
                        "slug": "royal-melbourne-hospital",
                        "description": "Royal Melbourne Hospital"
                    },
                    {
                        "name": "Rare Disease",
                        "slug": "rare-disease",
                        "description": "Rare disease panels"
                    }
                ],
                "child_panel_ids": []
            },
            "transcript": null
        },
        {
            "gene_data": {
                "alias": [
                    "PP1B",
                    "PP-1B",
                    "PP1beta"
                ],
                "biotype": "protein_coding",
                "hgnc_id": "HGNC:9282",
                "gene_name": "protein phosphatase 1 catalytic subunit beta",
                "omim_gene": [
                    "600590"
                ],
                "alias_name": null,
                "gene_symbol": "PPP1CB",
                "hgnc_symbol": "PPP1CB",
                "hgnc_release": "2017-11-03",
                "ensembl_genes": {
                    "GRch37": {
                        "82": {
                            "location": "2:28974506-29025806",
                            "ensembl_id": "ENSG00000213639"
                        }
                    },
                    "GRch38": {
                        "90": {
                            "location": "2:28751640-28802940",
                            "ensembl_id": "ENSG00000213639"
                        }
                    }
                },
                "hgnc_date_symbol_changed": "1993-01-22"
            },
            "entity_type": "gene",
            "entity_name": "PPP1CB",
            "confidence_level": "3",
            "penetrance": null,
            "mode_of_pathogenicity": "",
            "publications": [
                "27264673",
                "27681385",
                "28211982",
                "32476286",
                "27868344"
            ],
            "evidence": [
                "Expert Review Green",
                "Genomics England PanelApp",
                "Literature"
            ],
            "phenotypes": [
                "Noonan syndrome-like disorder with loose anagen hair 2",
                "OMIM # 617506"
            ],
            "mode_of_inheritance": "MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted",
            "tags": [],
            "panel": {
                "id": 3631,
                "hash_id": null,
                "name": "Growth failure",
                "disease_group": "",
                "disease_sub_group": "",
                "description": "This panel contains genes associated with growth failure in infancy/early childhood, either isolated or as part of another disorder.\r\n\r\nConsider applying this panel in individuals with:\r\n -Height Standard Deviation Score (SDS) <-3 (very significant short stature - well below the 0.4th centile)\r\nAND at least one of:\r\n- History of small for gestational age (birth weight and/or length <-2SDS)\r\n- Body disproportion, e.g. discrepancy between stature and head size\r\n- Dysmorphic features and congenital anomalies\r\n- Abnormalities in the GH-IGF axis (evidence of GH insensitivity or deficiency) and/or other pituitary hormonal deficiencies\r\n- Family history of significant short stature (1st and 2nd degree relatives) and/or consanguinity\r\n\r\nPrior to genomic testing consider:\r\n-Chromosomal microarray analysis (e.g. Turner syndrome)\r\n-Methylation analysis for Russell-Silver syndrome and Temple syndrome\r\n-Skeletal survey\r\n\r\nAcquired causes of short stature are relatively common.\r\n\r\nDepending on the specific clinical features present, consider applying the Skeletal dysplasia, Intellectual Disability, and/or Pituitary Hormone deficiency panels.\r\n\r\nWith thanks to Genomics England for the original design of this panel.",
                "status": "public",
                "version": "1.102",
                "version_created": "2026-04-01T10:17:12.005431+11:00",
                "relevant_disorders": [
                    "Failure to thrive",
                    "HP:0001508; Growth delay",
                    "HP:0001510"
                ],
                "stats": {
                    "number_of_genes": 204,
                    "number_of_strs": 0,
                    "number_of_regions": 4
                },
                "types": [
                    {
                        "name": "Victorian Clinical Genetics Services",
                        "slug": "victorian-clinical-genetics-services",
                        "description": "Panel used by VCGS."
                    },
                    {
                        "name": "Genetic Health Queensland",
                        "slug": "genetic-health-queensland",
                        "description": "Panel used by GHQ."
                    },
                    {
                        "name": "Royal Melbourne Hospital",
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                        "description": "Royal Melbourne Hospital"
                    },
                    {
                        "name": "Rare Disease",
                        "slug": "rare-disease",
                        "description": "Rare disease panels"
                    }
                ],
                "child_panel_ids": []
            },
            "transcript": null
        },
        {
            "gene_data": {
                "alias": [
                    "BPTP3",
                    "SH-PTP2",
                    "SHP-2",
                    "PTP2C",
                    "SHP2"
                ],
                "biotype": "protein_coding",
                "hgnc_id": "HGNC:9644",
                "gene_name": "protein tyrosine phosphatase, non-receptor type 11",
                "omim_gene": [
                    "176876"
                ],
                "alias_name": null,
                "gene_symbol": "PTPN11",
                "hgnc_symbol": "PTPN11",
                "hgnc_release": "2017-11-03",
                "ensembl_genes": {
                    "GRch37": {
                        "82": {
                            "location": "12:112856155-112947717",
                            "ensembl_id": "ENSG00000179295"
                        }
                    },
                    "GRch38": {
                        "90": {
                            "location": "12:112418351-112509913",
                            "ensembl_id": "ENSG00000179295"
                        }
                    }
                },
                "hgnc_date_symbol_changed": "1993-03-03"
            },
            "entity_type": "gene",
            "entity_name": "PTPN11",
            "confidence_level": "3",
            "penetrance": null,
            "mode_of_pathogenicity": "Loss-of-function variants (as defined in pop up message) DO NOT cause this phenotype - please provide details in the comments",
            "publications": [
                "16263833",
                "17603483",
                "17497712",
                "12634870",
                "11704759",
                "18678287",
                "15384080",
                "15240615",
                "12529711"
            ],
            "evidence": [
                "Expert Review Green",
                "Genomics England PanelApp"
            ],
            "phenotypes": [
                "LEOPARD syndrome 1, 151100 AD (for reporting use Noonan syndrome with multiple lentigines)",
                "Noonan syndrome 1, MIM#163950"
            ],
            "mode_of_inheritance": "MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted",
            "tags": [],
            "panel": {
                "id": 3631,
                "hash_id": null,
                "name": "Growth failure",
                "disease_group": "",
                "disease_sub_group": "",
                "description": "This panel contains genes associated with growth failure in infancy/early childhood, either isolated or as part of another disorder.\r\n\r\nConsider applying this panel in individuals with:\r\n -Height Standard Deviation Score (SDS) <-3 (very significant short stature - well below the 0.4th centile)\r\nAND at least one of:\r\n- History of small for gestational age (birth weight and/or length <-2SDS)\r\n- Body disproportion, e.g. discrepancy between stature and head size\r\n- Dysmorphic features and congenital anomalies\r\n- Abnormalities in the GH-IGF axis (evidence of GH insensitivity or deficiency) and/or other pituitary hormonal deficiencies\r\n- Family history of significant short stature (1st and 2nd degree relatives) and/or consanguinity\r\n\r\nPrior to genomic testing consider:\r\n-Chromosomal microarray analysis (e.g. Turner syndrome)\r\n-Methylation analysis for Russell-Silver syndrome and Temple syndrome\r\n-Skeletal survey\r\n\r\nAcquired causes of short stature are relatively common.\r\n\r\nDepending on the specific clinical features present, consider applying the Skeletal dysplasia, Intellectual Disability, and/or Pituitary Hormone deficiency panels.\r\n\r\nWith thanks to Genomics England for the original design of this panel.",
                "status": "public",
                "version": "1.102",
                "version_created": "2026-04-01T10:17:12.005431+11:00",
                "relevant_disorders": [
                    "Failure to thrive",
                    "HP:0001508; Growth delay",
                    "HP:0001510"
                ],
                "stats": {
                    "number_of_genes": 204,
                    "number_of_strs": 0,
                    "number_of_regions": 4
                },
                "types": [
                    {
                        "name": "Victorian Clinical Genetics Services",
                        "slug": "victorian-clinical-genetics-services",
                        "description": "Panel used by VCGS."
                    },
                    {
                        "name": "Genetic Health Queensland",
                        "slug": "genetic-health-queensland",
                        "description": "Panel used by GHQ."
                    },
                    {
                        "name": "Royal Melbourne Hospital",
                        "slug": "royal-melbourne-hospital",
                        "description": "Royal Melbourne Hospital"
                    },
                    {
                        "name": "Rare Disease",
                        "slug": "rare-disease",
                        "description": "Rare disease panels"
                    }
                ],
                "child_panel_ids": []
            },
            "transcript": null
        },
        {
            "gene_data": {
                "alias": [
                    "Raf-1",
                    "c-Raf",
                    "CRAF"
                ],
                "biotype": "protein_coding",
                "hgnc_id": "HGNC:9829",
                "gene_name": "Raf-1 proto-oncogene, serine/threonine kinase",
                "omim_gene": [
                    "164760"
                ],
                "alias_name": [
                    "C-Raf proto-oncogene, serine/threonine kinase"
                ],
                "gene_symbol": "RAF1",
                "hgnc_symbol": "RAF1",
                "hgnc_release": "2017-11-03",
                "ensembl_genes": {
                    "GRch37": {
                        "82": {
                            "location": "3:12625100-12705725",
                            "ensembl_id": "ENSG00000132155"
                        }
                    },
                    "GRch38": {
                        "90": {
                            "location": "3:12583601-12664226",
                            "ensembl_id": "ENSG00000132155"
                        }
                    }
                },
                "hgnc_date_symbol_changed": "1986-01-01"
            },
            "entity_type": "gene",
            "entity_name": "RAF1",
            "confidence_level": "3",
            "penetrance": null,
            "mode_of_pathogenicity": "Loss-of-function variants (as defined in pop up message) DO NOT cause this phenotype - please provide details in the comments",
            "publications": [
                "17603483",
                "17603482",
                "31145547",
                "31030682",
                "29271604"
            ],
            "evidence": [
                "Expert Review Green",
                "Genomics England PanelApp",
                "Victorian Clinical Genetics Services"
            ],
            "phenotypes": [
                "Noonan syndrome 5, MIM# 611553"
            ],
            "mode_of_inheritance": "MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted",
            "tags": [],
            "panel": {
                "id": 3631,
                "hash_id": null,
                "name": "Growth failure",
                "disease_group": "",
                "disease_sub_group": "",
                "description": "This panel contains genes associated with growth failure in infancy/early childhood, either isolated or as part of another disorder.\r\n\r\nConsider applying this panel in individuals with:\r\n -Height Standard Deviation Score (SDS) <-3 (very significant short stature - well below the 0.4th centile)\r\nAND at least one of:\r\n- History of small for gestational age (birth weight and/or length <-2SDS)\r\n- Body disproportion, e.g. discrepancy between stature and head size\r\n- Dysmorphic features and congenital anomalies\r\n- Abnormalities in the GH-IGF axis (evidence of GH insensitivity or deficiency) and/or other pituitary hormonal deficiencies\r\n- Family history of significant short stature (1st and 2nd degree relatives) and/or consanguinity\r\n\r\nPrior to genomic testing consider:\r\n-Chromosomal microarray analysis (e.g. Turner syndrome)\r\n-Methylation analysis for Russell-Silver syndrome and Temple syndrome\r\n-Skeletal survey\r\n\r\nAcquired causes of short stature are relatively common.\r\n\r\nDepending on the specific clinical features present, consider applying the Skeletal dysplasia, Intellectual Disability, and/or Pituitary Hormone deficiency panels.\r\n\r\nWith thanks to Genomics England for the original design of this panel.",
                "status": "public",
                "version": "1.102",
                "version_created": "2026-04-01T10:17:12.005431+11:00",
                "relevant_disorders": [
                    "Failure to thrive",
                    "HP:0001508; Growth delay",
                    "HP:0001510"
                ],
                "stats": {
                    "number_of_genes": 204,
                    "number_of_strs": 0,
                    "number_of_regions": 4
                },
                "types": [
                    {
                        "name": "Victorian Clinical Genetics Services",
                        "slug": "victorian-clinical-genetics-services",
                        "description": "Panel used by VCGS."
                    },
                    {
                        "name": "Genetic Health Queensland",
                        "slug": "genetic-health-queensland",
                        "description": "Panel used by GHQ."
                    },
                    {
                        "name": "Royal Melbourne Hospital",
                        "slug": "royal-melbourne-hospital",
                        "description": "Royal Melbourne Hospital"
                    },
                    {
                        "name": "Rare Disease",
                        "slug": "rare-disease",
                        "description": "Rare disease panels"
                    }
                ],
                "child_panel_ids": []
            },
            "transcript": null
        },
        {
            "gene_data": {
                "alias": [
                    "RIBB",
                    "ROC1",
                    "MGC125864",
                    "MGC125865"
                ],
                "biotype": "protein_coding",
                "hgnc_id": "HGNC:10023",
                "gene_name": "Ras like without CAAX 1",
                "omim_gene": [
                    "609591"
                ],
                "alias_name": [
                    "Ric-like, expressed in many tissues",
                    "GTP-binding protein Roc1"
                ],
                "gene_symbol": "RIT1",
                "hgnc_symbol": "RIT1",
                "hgnc_release": "2017-11-03",
                "ensembl_genes": {
                    "GRch37": {
                        "82": {
                            "location": "1:155867599-155881195",
                            "ensembl_id": "ENSG00000143622"
                        }
                    },
                    "GRch38": {
                        "90": {
                            "location": "1:155897808-155911404",
                            "ensembl_id": "ENSG00000143622"
                        }
                    }
                },
                "hgnc_date_symbol_changed": "2002-09-13"
            },
            "entity_type": "gene",
            "entity_name": "RIT1",
            "confidence_level": "3",
            "penetrance": null,
            "mode_of_pathogenicity": "Loss-of-function variants (as defined in pop up message) DO NOT cause this phenotype - please provide details in the comments",
            "publications": [
                "24939608",
                "25124994",
                "23791108",
                "27101134"
            ],
            "evidence": [
                "Expert Review Green",
                "Genomics England PanelApp",
                "Victorian Clinical Genetics Services"
            ],
            "phenotypes": [
                "Noonan syndrome 8, MIM# 615355"
            ],
            "mode_of_inheritance": "MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted",
            "tags": [],
            "panel": {
                "id": 3631,
                "hash_id": null,
                "name": "Growth failure",
                "disease_group": "",
                "disease_sub_group": "",
                "description": "This panel contains genes associated with growth failure in infancy/early childhood, either isolated or as part of another disorder.\r\n\r\nConsider applying this panel in individuals with:\r\n -Height Standard Deviation Score (SDS) <-3 (very significant short stature - well below the 0.4th centile)\r\nAND at least one of:\r\n- History of small for gestational age (birth weight and/or length <-2SDS)\r\n- Body disproportion, e.g. discrepancy between stature and head size\r\n- Dysmorphic features and congenital anomalies\r\n- Abnormalities in the GH-IGF axis (evidence of GH insensitivity or deficiency) and/or other pituitary hormonal deficiencies\r\n- Family history of significant short stature (1st and 2nd degree relatives) and/or consanguinity\r\n\r\nPrior to genomic testing consider:\r\n-Chromosomal microarray analysis (e.g. Turner syndrome)\r\n-Methylation analysis for Russell-Silver syndrome and Temple syndrome\r\n-Skeletal survey\r\n\r\nAcquired causes of short stature are relatively common.\r\n\r\nDepending on the specific clinical features present, consider applying the Skeletal dysplasia, Intellectual Disability, and/or Pituitary Hormone deficiency panels.\r\n\r\nWith thanks to Genomics England for the original design of this panel.",
                "status": "public",
                "version": "1.102",
                "version_created": "2026-04-01T10:17:12.005431+11:00",
                "relevant_disorders": [
                    "Failure to thrive",
                    "HP:0001508; Growth delay",
                    "HP:0001510"
                ],
                "stats": {
                    "number_of_genes": 204,
                    "number_of_strs": 0,
                    "number_of_regions": 4
                },
                "types": [
                    {
                        "name": "Victorian Clinical Genetics Services",
                        "slug": "victorian-clinical-genetics-services",
                        "description": "Panel used by VCGS."
                    },
                    {
                        "name": "Genetic Health Queensland",
                        "slug": "genetic-health-queensland",
                        "description": "Panel used by GHQ."
                    },
                    {
                        "name": "Royal Melbourne Hospital",
                        "slug": "royal-melbourne-hospital",
                        "description": "Royal Melbourne Hospital"
                    },
                    {
                        "name": "Rare Disease",
                        "slug": "rare-disease",
                        "description": "Rare disease panels"
                    }
                ],
                "child_panel_ids": []
            },
            "transcript": null
        },
        {
            "gene_data": {
                "alias": [
                    "KIAA0862",
                    "SOC2",
                    "SUR-8",
                    "SOC-2",
                    "SUR8"
                ],
                "biotype": "protein_coding",
                "hgnc_id": "HGNC:15454",
                "gene_name": "SHOC2, leucine rich repeat scaffold protein",
                "omim_gene": [
                    "602775"
                ],
                "alias_name": null,
                "gene_symbol": "SHOC2",
                "hgnc_symbol": "SHOC2",
                "hgnc_release": "2017-11-03",
                "ensembl_genes": {
                    "GRch37": {
                        "82": {
                            "location": "10:112679301-112773425",
                            "ensembl_id": "ENSG00000108061"
                        }
                    },
                    "GRch38": {
                        "90": {
                            "location": "10:110919547-111013667",
                            "ensembl_id": "ENSG00000108061"
                        }
                    }
                },
                "hgnc_date_symbol_changed": "2001-03-30"
            },
            "entity_type": "gene",
            "entity_name": "SHOC2",
            "confidence_level": "3",
            "penetrance": null,
            "mode_of_pathogenicity": "Loss-of-function variants (as defined in pop up message) DO NOT cause this phenotype - please provide details in the comments",
            "publications": [
                "23918763",
                "19684605",
                "22528146"
            ],
            "evidence": [
                "Expert Review Green",
                "Genomics England PanelApp",
                "Victorian Clinical Genetics Services"
            ],
            "phenotypes": [
                "Noonan syndrome-like with loose anagen hair 1, MIM# 607721"
            ],
            "mode_of_inheritance": "MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted",
            "tags": [],
            "panel": {
                "id": 3631,
                "hash_id": null,
                "name": "Growth failure",
                "disease_group": "",
                "disease_sub_group": "",
                "description": "This panel contains genes associated with growth failure in infancy/early childhood, either isolated or as part of another disorder.\r\n\r\nConsider applying this panel in individuals with:\r\n -Height Standard Deviation Score (SDS) <-3 (very significant short stature - well below the 0.4th centile)\r\nAND at least one of:\r\n- History of small for gestational age (birth weight and/or length <-2SDS)\r\n- Body disproportion, e.g. discrepancy between stature and head size\r\n- Dysmorphic features and congenital anomalies\r\n- Abnormalities in the GH-IGF axis (evidence of GH insensitivity or deficiency) and/or other pituitary hormonal deficiencies\r\n- Family history of significant short stature (1st and 2nd degree relatives) and/or consanguinity\r\n\r\nPrior to genomic testing consider:\r\n-Chromosomal microarray analysis (e.g. Turner syndrome)\r\n-Methylation analysis for Russell-Silver syndrome and Temple syndrome\r\n-Skeletal survey\r\n\r\nAcquired causes of short stature are relatively common.\r\n\r\nDepending on the specific clinical features present, consider applying the Skeletal dysplasia, Intellectual Disability, and/or Pituitary Hormone deficiency panels.\r\n\r\nWith thanks to Genomics England for the original design of this panel.",
                "status": "public",
                "version": "1.102",
                "version_created": "2026-04-01T10:17:12.005431+11:00",
                "relevant_disorders": [
                    "Failure to thrive",
                    "HP:0001508; Growth delay",
                    "HP:0001510"
                ],
                "stats": {
                    "number_of_genes": 204,
                    "number_of_strs": 0,
                    "number_of_regions": 4
                },
                "types": [
                    {
                        "name": "Victorian Clinical Genetics Services",
                        "slug": "victorian-clinical-genetics-services",
                        "description": "Panel used by VCGS."
                    },
                    {
                        "name": "Genetic Health Queensland",
                        "slug": "genetic-health-queensland",
                        "description": "Panel used by GHQ."
                    },
                    {
                        "name": "Royal Melbourne Hospital",
                        "slug": "royal-melbourne-hospital",
                        "description": "Royal Melbourne Hospital"
                    },
                    {
                        "name": "Rare Disease",
                        "slug": "rare-disease",
                        "description": "Rare disease panels"
                    }
                ],
                "child_panel_ids": []
            },
            "transcript": null
        },
        {
            "gene_data": {
                "alias": [
                    "KIAA1784",
                    "KIAA1987",
                    "FANCP"
                ],
                "biotype": "protein_coding",
                "hgnc_id": "HGNC:23845",
                "gene_name": "SLX4 structure-specific endonuclease subunit",
                "omim_gene": [
                    "613278"
                ],
                "alias_name": [
                    "Fanconi anemia, complementation group P"
                ],
                "gene_symbol": "SLX4",
                "hgnc_symbol": "SLX4",
                "hgnc_release": "2017-11-03",
                "ensembl_genes": {
                    "GRch37": {
                        "82": {
                            "location": "16:3631182-3661599",
                            "ensembl_id": "ENSG00000188827"
                        }
                    },
                    "GRch38": {
                        "90": {
                            "location": "16:3581181-3611598",
                            "ensembl_id": "ENSG00000188827"
                        }
                    }
                },
                "hgnc_date_symbol_changed": "2010-09-13"
            },
            "entity_type": "gene",
            "entity_name": "SLX4",
            "confidence_level": "3",
            "penetrance": null,
            "mode_of_pathogenicity": "",
            "publications": [
                "21240275",
                "21240277"
            ],
            "evidence": [
                "Expert Review Green",
                "Genomics England PanelApp",
                "Victorian Clinical Genetics Services",
                "Victorian Clinical Genetics Services"
            ],
            "phenotypes": [
                "Fanconi anemia, complementation group P, MIM# 613951"
            ],
            "mode_of_inheritance": "BIALLELIC, autosomal or pseudoautosomal",
            "tags": [],
            "panel": {
                "id": 3631,
                "hash_id": null,
                "name": "Growth failure",
                "disease_group": "",
                "disease_sub_group": "",
                "description": "This panel contains genes associated with growth failure in infancy/early childhood, either isolated or as part of another disorder.\r\n\r\nConsider applying this panel in individuals with:\r\n -Height Standard Deviation Score (SDS) <-3 (very significant short stature - well below the 0.4th centile)\r\nAND at least one of:\r\n- History of small for gestational age (birth weight and/or length <-2SDS)\r\n- Body disproportion, e.g. discrepancy between stature and head size\r\n- Dysmorphic features and congenital anomalies\r\n- Abnormalities in the GH-IGF axis (evidence of GH insensitivity or deficiency) and/or other pituitary hormonal deficiencies\r\n- Family history of significant short stature (1st and 2nd degree relatives) and/or consanguinity\r\n\r\nPrior to genomic testing consider:\r\n-Chromosomal microarray analysis (e.g. Turner syndrome)\r\n-Methylation analysis for Russell-Silver syndrome and Temple syndrome\r\n-Skeletal survey\r\n\r\nAcquired causes of short stature are relatively common.\r\n\r\nDepending on the specific clinical features present, consider applying the Skeletal dysplasia, Intellectual Disability, and/or Pituitary Hormone deficiency panels.\r\n\r\nWith thanks to Genomics England for the original design of this panel.",
                "status": "public",
                "version": "1.102",
                "version_created": "2026-04-01T10:17:12.005431+11:00",
                "relevant_disorders": [
                    "Failure to thrive",
                    "HP:0001508; Growth delay",
                    "HP:0001510"
                ],
                "stats": {
                    "number_of_genes": 204,
                    "number_of_strs": 0,
                    "number_of_regions": 4
                },
                "types": [
                    {
                        "name": "Victorian Clinical Genetics Services",
                        "slug": "victorian-clinical-genetics-services",
                        "description": "Panel used by VCGS."
                    },
                    {
                        "name": "Genetic Health Queensland",
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                    },
                    {
                        "name": "Royal Melbourne Hospital",
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                        "description": "Royal Melbourne Hospital"
                    },
                    {
                        "name": "Rare Disease",
                        "slug": "rare-disease",
                        "description": "Rare disease panels"
                    }
                ],
                "child_panel_ids": []
            },
            "transcript": null
        },
        {
            "gene_data": {
                "alias": [
                    "HGF",
                    "GF1"
                ],
                "biotype": "protein_coding",
                "hgnc_id": "HGNC:11187",
                "gene_name": "SOS Ras/Rac guanine nucleotide exchange factor 1",
                "omim_gene": [
                    "182530"
                ],
                "alias_name": null,
                "gene_symbol": "SOS1",
                "hgnc_symbol": "SOS1",
                "hgnc_release": "2017-11-03",
                "ensembl_genes": {
                    "GRch37": {
                        "82": {
                            "location": "2:39208537-39351486",
                            "ensembl_id": "ENSG00000115904"
                        }
                    },
                    "GRch38": {
                        "90": {
                            "location": "2:38981396-39124345",
                            "ensembl_id": "ENSG00000115904"
                        }
                    }
                },
                "hgnc_date_symbol_changed": "1993-10-27"
            },
            "entity_type": "gene",
            "entity_name": "SOS1",
            "confidence_level": "3",
            "penetrance": null,
            "mode_of_pathogenicity": "Loss-of-function variants (as defined in pop up message) DO NOT cause this phenotype - please provide details in the comments",
            "publications": [
                "17143285",
                "17586837",
                "17143282",
                "19438935"
            ],
            "evidence": [
                "Expert Review Green",
                "Genomics England PanelApp",
                "Victorian Clinical Genetics Services"
            ],
            "phenotypes": [
                "Noonan syndrome 4, MIM# 610733"
            ],
            "mode_of_inheritance": "MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted",
            "tags": [],
            "panel": {
                "id": 3631,
                "hash_id": null,
                "name": "Growth failure",
                "disease_group": "",
                "disease_sub_group": "",
                "description": "This panel contains genes associated with growth failure in infancy/early childhood, either isolated or as part of another disorder.\r\n\r\nConsider applying this panel in individuals with:\r\n -Height Standard Deviation Score (SDS) <-3 (very significant short stature - well below the 0.4th centile)\r\nAND at least one of:\r\n- History of small for gestational age (birth weight and/or length <-2SDS)\r\n- Body disproportion, e.g. discrepancy between stature and head size\r\n- Dysmorphic features and congenital anomalies\r\n- Abnormalities in the GH-IGF axis (evidence of GH insensitivity or deficiency) and/or other pituitary hormonal deficiencies\r\n- Family history of significant short stature (1st and 2nd degree relatives) and/or consanguinity\r\n\r\nPrior to genomic testing consider:\r\n-Chromosomal microarray analysis (e.g. Turner syndrome)\r\n-Methylation analysis for Russell-Silver syndrome and Temple syndrome\r\n-Skeletal survey\r\n\r\nAcquired causes of short stature are relatively common.\r\n\r\nDepending on the specific clinical features present, consider applying the Skeletal dysplasia, Intellectual Disability, and/or Pituitary Hormone deficiency panels.\r\n\r\nWith thanks to Genomics England for the original design of this panel.",
                "status": "public",
                "version": "1.102",
                "version_created": "2026-04-01T10:17:12.005431+11:00",
                "relevant_disorders": [
                    "Failure to thrive",
                    "HP:0001508; Growth delay",
                    "HP:0001510"
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                "stats": {
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                    "number_of_strs": 0,
                    "number_of_regions": 4
                },
                "types": [
                    {
                        "name": "Victorian Clinical Genetics Services",
                        "slug": "victorian-clinical-genetics-services",
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                    },
                    {
                        "name": "Genetic Health Queensland",
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                    {
                        "name": "Royal Melbourne Hospital",
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                    },
                    {
                        "name": "Rare Disease",
                        "slug": "rare-disease",
                        "description": "Rare disease panels"
                    }
                ],
                "child_panel_ids": []
            },
            "transcript": null
        },
        {
            "gene_data": {
                "alias": [],
                "biotype": "protein_coding",
                "hgnc_id": "HGNC:11188",
                "gene_name": "SOS Ras/Rho guanine nucleotide exchange factor 2",
                "omim_gene": [
                    "601247"
                ],
                "alias_name": null,
                "gene_symbol": "SOS2",
                "hgnc_symbol": "SOS2",
                "hgnc_release": "2017-11-03",
                "ensembl_genes": {
                    "GRch37": {
                        "82": {
                            "location": "14:50583847-50698276",
                            "ensembl_id": "ENSG00000100485"
                        }
                    },
                    "GRch38": {
                        "90": {
                            "location": "14:50117120-50231558",
                            "ensembl_id": "ENSG00000100485"
                        }
                    }
                },
                "hgnc_date_symbol_changed": "1993-10-27"
            },
            "entity_type": "gene",
            "entity_name": "SOS2",
            "confidence_level": "3",
            "penetrance": null,
            "mode_of_pathogenicity": "Loss-of-function variants (as defined in pop up message) DO NOT cause this phenotype - please provide details in the comments",
            "publications": [
                "25795793",
                "26173643",
                "32788663"
            ],
            "evidence": [
                "Expert Review Green",
                "Genomics England PanelApp",
                "Victorian Clinical Genetics Services"
            ],
            "phenotypes": [
                "Noonan syndrome 9, MIM# 616559"
            ],
            "mode_of_inheritance": "MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted",
            "tags": [],
            "panel": {
                "id": 3631,
                "hash_id": null,
                "name": "Growth failure",
                "disease_group": "",
                "disease_sub_group": "",
                "description": "This panel contains genes associated with growth failure in infancy/early childhood, either isolated or as part of another disorder.\r\n\r\nConsider applying this panel in individuals with:\r\n -Height Standard Deviation Score (SDS) <-3 (very significant short stature - well below the 0.4th centile)\r\nAND at least one of:\r\n- History of small for gestational age (birth weight and/or length <-2SDS)\r\n- Body disproportion, e.g. discrepancy between stature and head size\r\n- Dysmorphic features and congenital anomalies\r\n- Abnormalities in the GH-IGF axis (evidence of GH insensitivity or deficiency) and/or other pituitary hormonal deficiencies\r\n- Family history of significant short stature (1st and 2nd degree relatives) and/or consanguinity\r\n\r\nPrior to genomic testing consider:\r\n-Chromosomal microarray analysis (e.g. Turner syndrome)\r\n-Methylation analysis for Russell-Silver syndrome and Temple syndrome\r\n-Skeletal survey\r\n\r\nAcquired causes of short stature are relatively common.\r\n\r\nDepending on the specific clinical features present, consider applying the Skeletal dysplasia, Intellectual Disability, and/or Pituitary Hormone deficiency panels.\r\n\r\nWith thanks to Genomics England for the original design of this panel.",
                "status": "public",
                "version": "1.102",
                "version_created": "2026-04-01T10:17:12.005431+11:00",
                "relevant_disorders": [
                    "Failure to thrive",
                    "HP:0001508; Growth delay",
                    "HP:0001510"
                ],
                "stats": {
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                    "number_of_strs": 0,
                    "number_of_regions": 4
                },
                "types": [
                    {
                        "name": "Victorian Clinical Genetics Services",
                        "slug": "victorian-clinical-genetics-services",
                        "description": "Panel used by VCGS."
                    },
                    {
                        "name": "Genetic Health Queensland",
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                    {
                        "name": "Royal Melbourne Hospital",
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                    {
                        "name": "Rare Disease",
                        "slug": "rare-disease",
                        "description": "Rare disease panels"
                    }
                ],
                "child_panel_ids": []
            },
            "transcript": null
        },
        {
            "gene_data": {
                "alias": [
                    "KIAA0309",
                    "EAF1",
                    "SWR1",
                    "DOMO1"
                ],
                "biotype": "protein_coding",
                "hgnc_id": "HGNC:16974",
                "gene_name": "Snf2 related CREBBP activator protein",
                "omim_gene": [
                    "611421"
                ],
                "alias_name": [
                    "Swi2/Snf2-related ATPase homolog (S. cerevisiae)",
                    "domino homolog 1 (Drosophila)"
                ],
                "gene_symbol": "SRCAP",
                "hgnc_symbol": "SRCAP",
                "hgnc_release": "2017-11-03",
                "ensembl_genes": {
                    "GRch37": {
                        "82": {
                            "location": "16:30709530-30755602",
                            "ensembl_id": "ENSG00000080603"
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                    },
                    "GRch38": {
                        "90": {
                            "location": "16:30698209-30741409",
                            "ensembl_id": "ENSG00000080603"
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                    }
                },
                "hgnc_date_symbol_changed": "2007-11-29"
            },
            "entity_type": "gene",
            "entity_name": "SRCAP",
            "confidence_level": "3",
            "penetrance": null,
            "mode_of_pathogenicity": "",
            "publications": [
                "22265015",
                "22965468",
                "22965468"
            ],
            "evidence": [
                "Expert Review Green",
                "Genomics England PanelApp"
            ],
            "phenotypes": [
                "Floating-Harbor syndrome, OMIM # 136140"
            ],
            "mode_of_inheritance": "MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted",
            "tags": [],
            "panel": {
                "id": 3631,
                "hash_id": null,
                "name": "Growth failure",
                "disease_group": "",
                "disease_sub_group": "",
                "description": "This panel contains genes associated with growth failure in infancy/early childhood, either isolated or as part of another disorder.\r\n\r\nConsider applying this panel in individuals with:\r\n -Height Standard Deviation Score (SDS) <-3 (very significant short stature - well below the 0.4th centile)\r\nAND at least one of:\r\n- History of small for gestational age (birth weight and/or length <-2SDS)\r\n- Body disproportion, e.g. discrepancy between stature and head size\r\n- Dysmorphic features and congenital anomalies\r\n- Abnormalities in the GH-IGF axis (evidence of GH insensitivity or deficiency) and/or other pituitary hormonal deficiencies\r\n- Family history of significant short stature (1st and 2nd degree relatives) and/or consanguinity\r\n\r\nPrior to genomic testing consider:\r\n-Chromosomal microarray analysis (e.g. Turner syndrome)\r\n-Methylation analysis for Russell-Silver syndrome and Temple syndrome\r\n-Skeletal survey\r\n\r\nAcquired causes of short stature are relatively common.\r\n\r\nDepending on the specific clinical features present, consider applying the Skeletal dysplasia, Intellectual Disability, and/or Pituitary Hormone deficiency panels.\r\n\r\nWith thanks to Genomics England for the original design of this panel.",
                "status": "public",
                "version": "1.102",
                "version_created": "2026-04-01T10:17:12.005431+11:00",
                "relevant_disorders": [
                    "Failure to thrive",
                    "HP:0001508; Growth delay",
                    "HP:0001510"
                ],
                "stats": {
                    "number_of_genes": 204,
                    "number_of_strs": 0,
                    "number_of_regions": 4
                },
                "types": [
                    {
                        "name": "Victorian Clinical Genetics Services",
                        "slug": "victorian-clinical-genetics-services",
                        "description": "Panel used by VCGS."
                    },
                    {
                        "name": "Genetic Health Queensland",
                        "slug": "genetic-health-queensland",
                        "description": "Panel used by GHQ."
                    },
                    {
                        "name": "Royal Melbourne Hospital",
                        "slug": "royal-melbourne-hospital",
                        "description": "Royal Melbourne Hospital"
                    },
                    {
                        "name": "Rare Disease",
                        "slug": "rare-disease",
                        "description": "Rare disease panels"
                    }
                ],
                "child_panel_ids": []
            },
            "transcript": null
        },
        {
            "gene_data": {
                "alias": [
                    "ZGRF7"
                ],
                "biotype": "protein_coding",
                "hgnc_id": "HGNC:11992",
                "gene_name": "DNA topoisomerase III alpha",
                "omim_gene": [
                    "601243"
                ],
                "alias_name": [
                    "zinc finger, GRF-type containing 7"
                ],
                "gene_symbol": "TOP3A",
                "hgnc_symbol": "TOP3A",
                "hgnc_release": "2017-11-03",
                "ensembl_genes": {
                    "GRch37": {
                        "82": {
                            "location": "17:18174742-18218321",
                            "ensembl_id": "ENSG00000177302"
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                    },
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                        "90": {
                            "location": "17:18271428-18315007",
                            "ensembl_id": "ENSG00000177302"
                        }
                    }
                },
                "hgnc_date_symbol_changed": "1999-03-18"
            },
            "entity_type": "gene",
            "entity_name": "TOP3A",
            "confidence_level": "3",
            "penetrance": null,
            "mode_of_pathogenicity": "",
            "publications": [
                "30057030",
                "33631320"
            ],
            "evidence": [
                "Expert Review Green",
                "Genomics England PanelApp",
                "Victorian Clinical Genetics Services"
            ],
            "phenotypes": [
                "Microcephaly, growth restriction, and increased sister chromatid exchange 2, MIM# 618097"
            ],
            "mode_of_inheritance": "BIALLELIC, autosomal or pseudoautosomal",
            "tags": [],
            "panel": {
                "id": 3631,
                "hash_id": null,
                "name": "Growth failure",
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                "description": "This panel contains genes associated with growth failure in infancy/early childhood, either isolated or as part of another disorder.\r\n\r\nConsider applying this panel in individuals with:\r\n -Height Standard Deviation Score (SDS) <-3 (very significant short stature - well below the 0.4th centile)\r\nAND at least one of:\r\n- History of small for gestational age (birth weight and/or length <-2SDS)\r\n- Body disproportion, e.g. discrepancy between stature and head size\r\n- Dysmorphic features and congenital anomalies\r\n- Abnormalities in the GH-IGF axis (evidence of GH insensitivity or deficiency) and/or other pituitary hormonal deficiencies\r\n- Family history of significant short stature (1st and 2nd degree relatives) and/or consanguinity\r\n\r\nPrior to genomic testing consider:\r\n-Chromosomal microarray analysis (e.g. Turner syndrome)\r\n-Methylation analysis for Russell-Silver syndrome and Temple syndrome\r\n-Skeletal survey\r\n\r\nAcquired causes of short stature are relatively common.\r\n\r\nDepending on the specific clinical features present, consider applying the Skeletal dysplasia, Intellectual Disability, and/or Pituitary Hormone deficiency panels.\r\n\r\nWith thanks to Genomics England for the original design of this panel.",
                "status": "public",
                "version": "1.102",
                "version_created": "2026-04-01T10:17:12.005431+11:00",
                "relevant_disorders": [
                    "Failure to thrive",
                    "HP:0001508; Growth delay",
                    "HP:0001510"
                ],
                "stats": {
                    "number_of_genes": 204,
                    "number_of_strs": 0,
                    "number_of_regions": 4
                },
                "types": [
                    {
                        "name": "Victorian Clinical Genetics Services",
                        "slug": "victorian-clinical-genetics-services",
                        "description": "Panel used by VCGS."
                    },
                    {
                        "name": "Genetic Health Queensland",
                        "slug": "genetic-health-queensland",
                        "description": "Panel used by GHQ."
                    },
                    {
                        "name": "Royal Melbourne Hospital",
                        "slug": "royal-melbourne-hospital",
                        "description": "Royal Melbourne Hospital"
                    },
                    {
                        "name": "Rare Disease",
                        "slug": "rare-disease",
                        "description": "Rare disease panels"
                    }
                ],
                "child_panel_ids": []
            },
            "transcript": null
        },
        {
            "gene_data": {
                "alias": [
                    "KIAA0898",
                    "POB1",
                    "TEF3"
                ],
                "biotype": "protein_coding",
                "hgnc_id": "HGNC:7523",
                "gene_name": "tripartite motif containing 37",
                "omim_gene": [
                    "605073"
                ],
                "alias_name": [
                    "RING-B-box-coiled-coil protein"
                ],
                "gene_symbol": "TRIM37",
                "hgnc_symbol": "TRIM37",
                "hgnc_release": "2017-11-03",
                "ensembl_genes": {
                    "GRch37": {
                        "82": {
                            "location": "17:57059999-57184282",
                            "ensembl_id": "ENSG00000108395"
                        }
                    },
                    "GRch38": {
                        "90": {
                            "location": "17:58982638-59106921",
                            "ensembl_id": "ENSG00000108395"
                        }
                    }
                },
                "hgnc_date_symbol_changed": "2001-11-30"
            },
            "entity_type": "gene",
            "entity_name": "TRIM37",
            "confidence_level": "3",
            "penetrance": null,
            "mode_of_pathogenicity": "",
            "publications": [
                "10888877",
                "12754710",
                "15108285",
                "14757854",
                "27044324"
            ],
            "evidence": [
                "Expert Review Green",
                "Genomics England PanelApp"
            ],
            "phenotypes": [
                "Mulibery nanism, MIM#253250"
            ],
            "mode_of_inheritance": "BIALLELIC, autosomal or pseudoautosomal",
            "tags": [],
            "panel": {
                "id": 3631,
                "hash_id": null,
                "name": "Growth failure",
                "disease_group": "",
                "disease_sub_group": "",
                "description": "This panel contains genes associated with growth failure in infancy/early childhood, either isolated or as part of another disorder.\r\n\r\nConsider applying this panel in individuals with:\r\n -Height Standard Deviation Score (SDS) <-3 (very significant short stature - well below the 0.4th centile)\r\nAND at least one of:\r\n- History of small for gestational age (birth weight and/or length <-2SDS)\r\n- Body disproportion, e.g. discrepancy between stature and head size\r\n- Dysmorphic features and congenital anomalies\r\n- Abnormalities in the GH-IGF axis (evidence of GH insensitivity or deficiency) and/or other pituitary hormonal deficiencies\r\n- Family history of significant short stature (1st and 2nd degree relatives) and/or consanguinity\r\n\r\nPrior to genomic testing consider:\r\n-Chromosomal microarray analysis (e.g. Turner syndrome)\r\n-Methylation analysis for Russell-Silver syndrome and Temple syndrome\r\n-Skeletal survey\r\n\r\nAcquired causes of short stature are relatively common.\r\n\r\nDepending on the specific clinical features present, consider applying the Skeletal dysplasia, Intellectual Disability, and/or Pituitary Hormone deficiency panels.\r\n\r\nWith thanks to Genomics England for the original design of this panel.",
                "status": "public",
                "version": "1.102",
                "version_created": "2026-04-01T10:17:12.005431+11:00",
                "relevant_disorders": [
                    "Failure to thrive",
                    "HP:0001508; Growth delay",
                    "HP:0001510"
                ],
                "stats": {
                    "number_of_genes": 204,
                    "number_of_strs": 0,
                    "number_of_regions": 4
                },
                "types": [
                    {
                        "name": "Victorian Clinical Genetics Services",
                        "slug": "victorian-clinical-genetics-services",
                        "description": "Panel used by VCGS."
                    },
                    {
                        "name": "Genetic Health Queensland",
                        "slug": "genetic-health-queensland",
                        "description": "Panel used by GHQ."
                    },
                    {
                        "name": "Royal Melbourne Hospital",
                        "slug": "royal-melbourne-hospital",
                        "description": "Royal Melbourne Hospital"
                    },
                    {
                        "name": "Rare Disease",
                        "slug": "rare-disease",
                        "description": "Rare disease panels"
                    }
                ],
                "child_panel_ids": []
            },
            "transcript": null
        },
        {
            "gene_data": {
                "alias": [
                    "HSPC150",
                    "FANCT"
                ],
                "biotype": "protein_coding",
                "hgnc_id": "HGNC:25009",
                "gene_name": "ubiquitin conjugating enzyme E2 T",
                "omim_gene": [
                    "610538"
                ],
                "alias_name": null,
                "gene_symbol": "UBE2T",
                "hgnc_symbol": "UBE2T",
                "hgnc_release": "2017-11-03",
                "ensembl_genes": {
                    "GRch37": {
                        "82": {
                            "location": "1:202300785-202311108",
                            "ensembl_id": "ENSG00000077152"
                        }
                    },
                    "GRch38": {
                        "90": {
                            "location": "1:202331657-202341980",
                            "ensembl_id": "ENSG00000077152"
                        }
                    }
                },
                "hgnc_date_symbol_changed": "2005-03-21"
            },
            "entity_type": "gene",
            "entity_name": "UBE2T",
            "confidence_level": "3",
            "penetrance": null,
            "mode_of_pathogenicity": "",
            "publications": [
                "26046368",
                "32646888"
            ],
            "evidence": [
                "Expert Review Green",
                "Genomics England PanelApp",
                "Victorian Clinical Genetics Services"
            ],
            "phenotypes": [
                "Fanconi anemia, complementation group T, MIM# 616435"
            ],
            "mode_of_inheritance": "BIALLELIC, autosomal or pseudoautosomal",
            "tags": [],
            "panel": {
                "id": 3631,
                "hash_id": null,
                "name": "Growth failure",
                "disease_group": "",
                "disease_sub_group": "",
                "description": "This panel contains genes associated with growth failure in infancy/early childhood, either isolated or as part of another disorder.\r\n\r\nConsider applying this panel in individuals with:\r\n -Height Standard Deviation Score (SDS) <-3 (very significant short stature - well below the 0.4th centile)\r\nAND at least one of:\r\n- History of small for gestational age (birth weight and/or length <-2SDS)\r\n- Body disproportion, e.g. discrepancy between stature and head size\r\n- Dysmorphic features and congenital anomalies\r\n- Abnormalities in the GH-IGF axis (evidence of GH insensitivity or deficiency) and/or other pituitary hormonal deficiencies\r\n- Family history of significant short stature (1st and 2nd degree relatives) and/or consanguinity\r\n\r\nPrior to genomic testing consider:\r\n-Chromosomal microarray analysis (e.g. Turner syndrome)\r\n-Methylation analysis for Russell-Silver syndrome and Temple syndrome\r\n-Skeletal survey\r\n\r\nAcquired causes of short stature are relatively common.\r\n\r\nDepending on the specific clinical features present, consider applying the Skeletal dysplasia, Intellectual Disability, and/or Pituitary Hormone deficiency panels.\r\n\r\nWith thanks to Genomics England for the original design of this panel.",
                "status": "public",
                "version": "1.102",
                "version_created": "2026-04-01T10:17:12.005431+11:00",
                "relevant_disorders": [
                    "Failure to thrive",
                    "HP:0001508; Growth delay",
                    "HP:0001510"
                ],
                "stats": {
                    "number_of_genes": 204,
                    "number_of_strs": 0,
                    "number_of_regions": 4
                },
                "types": [
                    {
                        "name": "Victorian Clinical Genetics Services",
                        "slug": "victorian-clinical-genetics-services",
                        "description": "Panel used by VCGS."
                    },
                    {
                        "name": "Genetic Health Queensland",
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                        "description": "Panel used by GHQ."
                    },
                    {
                        "name": "Royal Melbourne Hospital",
                        "slug": "royal-melbourne-hospital",
                        "description": "Royal Melbourne Hospital"
                    },
                    {
                        "name": "Rare Disease",
                        "slug": "rare-disease",
                        "description": "Rare disease panels"
                    }
                ],
                "child_panel_ids": []
            },
            "transcript": null
        },
        {
            "gene_data": {
                "alias": [
                    "MCPR",
                    "TSG24",
                    "APC1"
                ],
                "biotype": "protein_coding",
                "hgnc_id": "HGNC:19988",
                "gene_name": "anaphase promoting complex subunit 1",
                "omim_gene": [
                    "608473"
                ],
                "alias_name": null,
                "gene_symbol": "ANAPC1",
                "hgnc_symbol": "ANAPC1",
                "hgnc_release": "2017-11-03",
                "ensembl_genes": {
                    "GRch37": {
                        "82": {
                            "location": "2:112523848-112642267",
                            "ensembl_id": "ENSG00000153107"
                        }
                    },
                    "GRch38": {
                        "90": {
                            "location": "2:111766271-111884690",
                            "ensembl_id": "ENSG00000153107"
                        }
                    }
                },
                "hgnc_date_symbol_changed": "2004-01-13"
            },
            "entity_type": "gene",
            "entity_name": "ANAPC1",
            "confidence_level": "3",
            "penetrance": null,
            "mode_of_pathogenicity": "",
            "publications": [
                "31303264"
            ],
            "evidence": [
                "Expert Review Green",
                "Genomics England PanelApp"
            ],
            "phenotypes": [
                "Rothmund Thomson syndrome type 1, OMIM:618625, MONDO:0016368"
            ],
            "mode_of_inheritance": "BIALLELIC, autosomal or pseudoautosomal",
            "tags": [
                "deep intronic"
            ],
            "panel": {
                "id": 3631,
                "hash_id": null,
                "name": "Growth failure",
                "disease_group": "",
                "disease_sub_group": "",
                "description": "This panel contains genes associated with growth failure in infancy/early childhood, either isolated or as part of another disorder.\r\n\r\nConsider applying this panel in individuals with:\r\n -Height Standard Deviation Score (SDS) <-3 (very significant short stature - well below the 0.4th centile)\r\nAND at least one of:\r\n- History of small for gestational age (birth weight and/or length <-2SDS)\r\n- Body disproportion, e.g. discrepancy between stature and head size\r\n- Dysmorphic features and congenital anomalies\r\n- Abnormalities in the GH-IGF axis (evidence of GH insensitivity or deficiency) and/or other pituitary hormonal deficiencies\r\n- Family history of significant short stature (1st and 2nd degree relatives) and/or consanguinity\r\n\r\nPrior to genomic testing consider:\r\n-Chromosomal microarray analysis (e.g. Turner syndrome)\r\n-Methylation analysis for Russell-Silver syndrome and Temple syndrome\r\n-Skeletal survey\r\n\r\nAcquired causes of short stature are relatively common.\r\n\r\nDepending on the specific clinical features present, consider applying the Skeletal dysplasia, Intellectual Disability, and/or Pituitary Hormone deficiency panels.\r\n\r\nWith thanks to Genomics England for the original design of this panel.",
                "status": "public",
                "version": "1.102",
                "version_created": "2026-04-01T10:17:12.005431+11:00",
                "relevant_disorders": [
                    "Failure to thrive",
                    "HP:0001508; Growth delay",
                    "HP:0001510"
                ],
                "stats": {
                    "number_of_genes": 204,
                    "number_of_strs": 0,
                    "number_of_regions": 4
                },
                "types": [
                    {
                        "name": "Victorian Clinical Genetics Services",
                        "slug": "victorian-clinical-genetics-services",
                        "description": "Panel used by VCGS."
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                    {
                        "name": "Genetic Health Queensland",
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                        "name": "Rare Disease",
                        "slug": "rare-disease",
                        "description": "Rare disease panels"
                    }
                ],
                "child_panel_ids": []
            },
            "transcript": null
        },
        {
            "gene_data": {
                "alias": [
                    "Translokin",
                    "TSP57",
                    "KIAA0092"
                ],
                "biotype": "protein_coding",
                "hgnc_id": "HGNC:30794",
                "gene_name": "centrosomal protein 57",
                "omim_gene": [
                    "607951"
                ],
                "alias_name": null,
                "gene_symbol": "CEP57",
                "hgnc_symbol": "CEP57",
                "hgnc_release": "2017-11-03",
                "ensembl_genes": {
                    "GRch37": {
                        "82": {
                            "location": "11:95523129-95565857",
                            "ensembl_id": "ENSG00000166037"
                        }
                    },
                    "GRch38": {
                        "90": {
                            "location": "11:95789965-95832693",
                            "ensembl_id": "ENSG00000166037"
                        }
                    }
                },
                "hgnc_date_symbol_changed": "2005-12-02"
            },
            "entity_type": "gene",
            "entity_name": "CEP57",
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            "penetrance": null,
            "mode_of_pathogenicity": "",
            "publications": [
                "24259107",
                "21552266",
                "30147898",
                "32861809"
            ],
            "evidence": [
                "Expert Review Green",
                "Genomics England PanelApp"
            ],
            "phenotypes": [
                "Mosaic variegated aneuploidy syndrome 2, MIM#614114"
            ],
            "mode_of_inheritance": "BIALLELIC, autosomal or pseudoautosomal",
            "tags": [],
            "panel": {
                "id": 3631,
                "hash_id": null,
                "name": "Growth failure",
                "disease_group": "",
                "disease_sub_group": "",
                "description": "This panel contains genes associated with growth failure in infancy/early childhood, either isolated or as part of another disorder.\r\n\r\nConsider applying this panel in individuals with:\r\n -Height Standard Deviation Score (SDS) <-3 (very significant short stature - well below the 0.4th centile)\r\nAND at least one of:\r\n- History of small for gestational age (birth weight and/or length <-2SDS)\r\n- Body disproportion, e.g. discrepancy between stature and head size\r\n- Dysmorphic features and congenital anomalies\r\n- Abnormalities in the GH-IGF axis (evidence of GH insensitivity or deficiency) and/or other pituitary hormonal deficiencies\r\n- Family history of significant short stature (1st and 2nd degree relatives) and/or consanguinity\r\n\r\nPrior to genomic testing consider:\r\n-Chromosomal microarray analysis (e.g. Turner syndrome)\r\n-Methylation analysis for Russell-Silver syndrome and Temple syndrome\r\n-Skeletal survey\r\n\r\nAcquired causes of short stature are relatively common.\r\n\r\nDepending on the specific clinical features present, consider applying the Skeletal dysplasia, Intellectual Disability, and/or Pituitary Hormone deficiency panels.\r\n\r\nWith thanks to Genomics England for the original design of this panel.",
                "status": "public",
                "version": "1.102",
                "version_created": "2026-04-01T10:17:12.005431+11:00",
                "relevant_disorders": [
                    "Failure to thrive",
                    "HP:0001508; Growth delay",
                    "HP:0001510"
                ],
                "stats": {
                    "number_of_genes": 204,
                    "number_of_strs": 0,
                    "number_of_regions": 4
                },
                "types": [
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                        "name": "Victorian Clinical Genetics Services",
                        "slug": "victorian-clinical-genetics-services",
                        "description": "Panel used by VCGS."
                    },
                    {
                        "name": "Genetic Health Queensland",
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                    {
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                        "name": "Rare Disease",
                        "slug": "rare-disease",
                        "description": "Rare disease panels"
                    }
                ],
                "child_panel_ids": []
            },
            "transcript": null
        },
        {
            "gene_data": {
                "alias": [
                    "COD1",
                    "DKFZP586E1519"
                ],
                "biotype": "protein_coding",
                "hgnc_id": "HGNC:18620",
                "gene_name": "component of oligomeric golgi complex 4",
                "omim_gene": [
                    "606976"
                ],
                "alias_name": null,
                "gene_symbol": "COG4",
                "hgnc_symbol": "COG4",
                "hgnc_release": "2017-11-03",
                "ensembl_genes": {
                    "GRch37": {
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                            "location": "16:70514471-70557468",
                            "ensembl_id": "ENSG00000103051"
                        }
                    },
                    "GRch38": {
                        "90": {
                            "location": "16:70480568-70523565",
                            "ensembl_id": "ENSG00000103051"
                        }
                    }
                },
                "hgnc_date_symbol_changed": "2002-05-09"
            },
            "entity_type": "gene",
            "entity_name": "COG4",
            "confidence_level": "3",
            "penetrance": null,
            "mode_of_pathogenicity": "Other",
            "publications": [
                "30290151",
                "31949312"
            ],
            "evidence": [
                "Expert Review Green",
                "Genomics England PanelApp"
            ],
            "phenotypes": [
                "Saul-Wilson syndrome, OMIM:618150",
                "Microcephalic osteodysplastic dysplasia, Saul-Wilson type, MONDO:0019407"
            ],
            "mode_of_inheritance": "MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown",
            "tags": [],
            "panel": {
                "id": 3631,
                "hash_id": null,
                "name": "Growth failure",
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                "description": "This panel contains genes associated with growth failure in infancy/early childhood, either isolated or as part of another disorder.\r\n\r\nConsider applying this panel in individuals with:\r\n -Height Standard Deviation Score (SDS) <-3 (very significant short stature - well below the 0.4th centile)\r\nAND at least one of:\r\n- History of small for gestational age (birth weight and/or length <-2SDS)\r\n- Body disproportion, e.g. discrepancy between stature and head size\r\n- Dysmorphic features and congenital anomalies\r\n- Abnormalities in the GH-IGF axis (evidence of GH insensitivity or deficiency) and/or other pituitary hormonal deficiencies\r\n- Family history of significant short stature (1st and 2nd degree relatives) and/or consanguinity\r\n\r\nPrior to genomic testing consider:\r\n-Chromosomal microarray analysis (e.g. Turner syndrome)\r\n-Methylation analysis for Russell-Silver syndrome and Temple syndrome\r\n-Skeletal survey\r\n\r\nAcquired causes of short stature are relatively common.\r\n\r\nDepending on the specific clinical features present, consider applying the Skeletal dysplasia, Intellectual Disability, and/or Pituitary Hormone deficiency panels.\r\n\r\nWith thanks to Genomics England for the original design of this panel.",
                "status": "public",
                "version": "1.102",
                "version_created": "2026-04-01T10:17:12.005431+11:00",
                "relevant_disorders": [
                    "Failure to thrive",
                    "HP:0001508; Growth delay",
                    "HP:0001510"
                ],
                "stats": {
                    "number_of_genes": 204,
                    "number_of_strs": 0,
                    "number_of_regions": 4
                },
                "types": [
                    {
                        "name": "Victorian Clinical Genetics Services",
                        "slug": "victorian-clinical-genetics-services",
                        "description": "Panel used by VCGS."
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                    {
                        "name": "Genetic Health Queensland",
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                        "name": "Royal Melbourne Hospital",
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                    {
                        "name": "Rare Disease",
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                    }
                ],
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            "transcript": null
        },
        {
            "gene_data": {
                "alias": [
                    "FLJ40908"
                ],
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                    "608924"
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                "alias_name": null,
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                "hgnc_symbol": "FOXP4",
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                "hgnc_date_symbol_changed": "2003-05-28"
            },
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                "Genomics England PanelApp"
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                "Neurodevelopmental disorder",
                "multiple congenital abnormalities",
                "short stature"
            ],
            "mode_of_inheritance": "MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted",
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                "status": "public",
                "version": "1.102",
                "version_created": "2026-04-01T10:17:12.005431+11:00",
                "relevant_disorders": [
                    "Failure to thrive",
                    "HP:0001508; Growth delay",
                    "HP:0001510"
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                "stats": {
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                    "number_of_strs": 0,
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                "types": [
                    {
                        "name": "Victorian Clinical Genetics Services",
                        "slug": "victorian-clinical-genetics-services",
                        "description": "Panel used by VCGS."
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                    {
                        "name": "Genetic Health Queensland",
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                        "name": "Royal Melbourne Hospital",
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                    {
                        "name": "Rare Disease",
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                        "description": "Rare disease panels"
                    }
                ],
                "child_panel_ids": []
            },
            "transcript": null
        },
        {
            "gene_data": {
                "alias": [
                    "DKFZp586J0619",
                    "KIAA1440",
                    "INT1",
                    "NET28"
                ],
                "biotype": "protein_coding",
                "hgnc_id": "HGNC:24555",
                "gene_name": "integrator complex subunit 1",
                "omim_gene": [
                    "611345"
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                "alias_name": null,
                "gene_symbol": "INTS1",
                "hgnc_symbol": "INTS1",
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                "ensembl_genes": {
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                            "location": "7:1509913-1545489",
                            "ensembl_id": "ENSG00000164880"
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                "hgnc_date_symbol_changed": "2006-03-15"
            },
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                "28542170",
                "31428919",
                "30622326"
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            "phenotypes": [
                "Neurodevelopmental disorder with cataracts, poor growth, and dysmorphic facies, OMIM:618571, MONDO:0032817"
            ],
            "mode_of_inheritance": "BIALLELIC, autosomal or pseudoautosomal",
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            "panel": {
                "id": 3631,
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                "description": "This panel contains genes associated with growth failure in infancy/early childhood, either isolated or as part of another disorder.\r\n\r\nConsider applying this panel in individuals with:\r\n -Height Standard Deviation Score (SDS) <-3 (very significant short stature - well below the 0.4th centile)\r\nAND at least one of:\r\n- History of small for gestational age (birth weight and/or length <-2SDS)\r\n- Body disproportion, e.g. discrepancy between stature and head size\r\n- Dysmorphic features and congenital anomalies\r\n- Abnormalities in the GH-IGF axis (evidence of GH insensitivity or deficiency) and/or other pituitary hormonal deficiencies\r\n- Family history of significant short stature (1st and 2nd degree relatives) and/or consanguinity\r\n\r\nPrior to genomic testing consider:\r\n-Chromosomal microarray analysis (e.g. Turner syndrome)\r\n-Methylation analysis for Russell-Silver syndrome and Temple syndrome\r\n-Skeletal survey\r\n\r\nAcquired causes of short stature are relatively common.\r\n\r\nDepending on the specific clinical features present, consider applying the Skeletal dysplasia, Intellectual Disability, and/or Pituitary Hormone deficiency panels.\r\n\r\nWith thanks to Genomics England for the original design of this panel.",
                "status": "public",
                "version": "1.102",
                "version_created": "2026-04-01T10:17:12.005431+11:00",
                "relevant_disorders": [
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                    "HP:0001508; Growth delay",
                    "HP:0001510"
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                "stats": {
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                    "number_of_strs": 0,
                    "number_of_regions": 4
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                "types": [
                    {
                        "name": "Victorian Clinical Genetics Services",
                        "slug": "victorian-clinical-genetics-services",
                        "description": "Panel used by VCGS."
                    },
                    {
                        "name": "Genetic Health Queensland",
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                    {
                        "name": "Royal Melbourne Hospital",
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                    {
                        "name": "Rare Disease",
                        "slug": "rare-disease",
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                    }
                ],
                "child_panel_ids": []
            },
            "transcript": null
        },
        {
            "gene_data": {
                "alias": [
                    "KIAA1082",
                    "NET22"
                ],
                "biotype": "protein_coding",
                "hgnc_id": "HGNC:1337",
                "gene_name": "lysine demethylase 3B",
                "omim_gene": [
                    "609373"
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                "alias_name": null,
                "gene_symbol": "KDM3B",
                "hgnc_symbol": "KDM3B",
                "hgnc_release": "2017-11-03",
                "ensembl_genes": {
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                            "location": "5:137688285-137772717",
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                            "ensembl_id": "ENSG00000120733"
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                "hgnc_date_symbol_changed": "2009-04-06"
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                "30929739"
            ],
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                "Expert Review Green",
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            ],
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                "Diets-Jongmans syndrome, MIM# 618846",
                "Intellectual disability",
                "short stature",
                "deafness"
            ],
            "mode_of_inheritance": "MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted",
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            "panel": {
                "id": 3631,
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                "description": "This panel contains genes associated with growth failure in infancy/early childhood, either isolated or as part of another disorder.\r\n\r\nConsider applying this panel in individuals with:\r\n -Height Standard Deviation Score (SDS) <-3 (very significant short stature - well below the 0.4th centile)\r\nAND at least one of:\r\n- History of small for gestational age (birth weight and/or length <-2SDS)\r\n- Body disproportion, e.g. discrepancy between stature and head size\r\n- Dysmorphic features and congenital anomalies\r\n- Abnormalities in the GH-IGF axis (evidence of GH insensitivity or deficiency) and/or other pituitary hormonal deficiencies\r\n- Family history of significant short stature (1st and 2nd degree relatives) and/or consanguinity\r\n\r\nPrior to genomic testing consider:\r\n-Chromosomal microarray analysis (e.g. Turner syndrome)\r\n-Methylation analysis for Russell-Silver syndrome and Temple syndrome\r\n-Skeletal survey\r\n\r\nAcquired causes of short stature are relatively common.\r\n\r\nDepending on the specific clinical features present, consider applying the Skeletal dysplasia, Intellectual Disability, and/or Pituitary Hormone deficiency panels.\r\n\r\nWith thanks to Genomics England for the original design of this panel.",
                "status": "public",
                "version": "1.102",
                "version_created": "2026-04-01T10:17:12.005431+11:00",
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                    "HP:0001508; Growth delay",
                    "HP:0001510"
                ],
                "stats": {
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                },
                "types": [
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                    {
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                        "name": "Rare Disease",
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                        "description": "Rare disease panels"
                    }
                ],
                "child_panel_ids": []
            },
            "transcript": null
        },
        {
            "gene_data": {
                "alias": [
                    "FLJ10504",
                    "LST005",
                    "MST",
                    "misato"
                ],
                "biotype": "protein_coding",
                "hgnc_id": "HGNC:29678",
                "gene_name": "misato 1, mitochondrial distribution and morphology regulator",
                "omim_gene": [
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                "alias_name": null,
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                "ensembl_genes": {
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                            "location": "1:155579979-155718153",
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                "hgnc_date_symbol_changed": "2005-07-19"
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            "publications": [
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                "28554942",
                "31604776",
                "28544275",
                "31130378"
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            "evidence": [
                "Expert Review Green",
                "Genomics England PanelApp"
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            "phenotypes": [
                "Myopathy, mitochondrial, and ataxia, OMIM:617675"
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            "mode_of_inheritance": "BIALLELIC, autosomal or pseudoautosomal",
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            "panel": {
                "id": 3631,
                "hash_id": null,
                "name": "Growth failure",
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                "description": "This panel contains genes associated with growth failure in infancy/early childhood, either isolated or as part of another disorder.\r\n\r\nConsider applying this panel in individuals with:\r\n -Height Standard Deviation Score (SDS) <-3 (very significant short stature - well below the 0.4th centile)\r\nAND at least one of:\r\n- History of small for gestational age (birth weight and/or length <-2SDS)\r\n- Body disproportion, e.g. discrepancy between stature and head size\r\n- Dysmorphic features and congenital anomalies\r\n- Abnormalities in the GH-IGF axis (evidence of GH insensitivity or deficiency) and/or other pituitary hormonal deficiencies\r\n- Family history of significant short stature (1st and 2nd degree relatives) and/or consanguinity\r\n\r\nPrior to genomic testing consider:\r\n-Chromosomal microarray analysis (e.g. Turner syndrome)\r\n-Methylation analysis for Russell-Silver syndrome and Temple syndrome\r\n-Skeletal survey\r\n\r\nAcquired causes of short stature are relatively common.\r\n\r\nDepending on the specific clinical features present, consider applying the Skeletal dysplasia, Intellectual Disability, and/or Pituitary Hormone deficiency panels.\r\n\r\nWith thanks to Genomics England for the original design of this panel.",
                "status": "public",
                "version": "1.102",
                "version_created": "2026-04-01T10:17:12.005431+11:00",
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                    "Failure to thrive",
                    "HP:0001508; Growth delay",
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                "stats": {
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                },
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                    }
                ],
                "child_panel_ids": []
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            "transcript": null
        },
        {
            "gene_data": {
                "alias": [],
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                "hgnc_id": "HGNC:7506",
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                "alias_name": null,
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                "hgnc_symbol": "MTX2",
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                            "location": "2:177134123-177202753",
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            "entity_type": "gene",
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                "arterial calcification",
                "lipodystrophy"
            ],
            "mode_of_inheritance": "BIALLELIC, autosomal or pseudoautosomal",
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            "panel": {
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                "version_created": "2026-04-01T10:17:12.005431+11:00",
                "relevant_disorders": [
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                    "HP:0001508; Growth delay",
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        {
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                "hgnc_id": "HGNC:24731",
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                "32435055"
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                "Genomics England PanelApp"
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                "Fibrosis, neurodegeneration, and cerebral angiomatosis (FINCA) syndrome MIM#618278"
            ],
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                "description": "This panel contains genes associated with growth failure in infancy/early childhood, either isolated or as part of another disorder.\r\n\r\nConsider applying this panel in individuals with:\r\n -Height Standard Deviation Score (SDS) <-3 (very significant short stature - well below the 0.4th centile)\r\nAND at least one of:\r\n- History of small for gestational age (birth weight and/or length <-2SDS)\r\n- Body disproportion, e.g. discrepancy between stature and head size\r\n- Dysmorphic features and congenital anomalies\r\n- Abnormalities in the GH-IGF axis (evidence of GH insensitivity or deficiency) and/or other pituitary hormonal deficiencies\r\n- Family history of significant short stature (1st and 2nd degree relatives) and/or consanguinity\r\n\r\nPrior to genomic testing consider:\r\n-Chromosomal microarray analysis (e.g. Turner syndrome)\r\n-Methylation analysis for Russell-Silver syndrome and Temple syndrome\r\n-Skeletal survey\r\n\r\nAcquired causes of short stature are relatively common.\r\n\r\nDepending on the specific clinical features present, consider applying the Skeletal dysplasia, Intellectual Disability, and/or Pituitary Hormone deficiency panels.\r\n\r\nWith thanks to Genomics England for the original design of this panel.",
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                "version": "1.102",
                "version_created": "2026-04-01T10:17:12.005431+11:00",
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                    "Failure to thrive",
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                "stats": {
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                },
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                        "name": "Victorian Clinical Genetics Services",
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                    {
                        "name": "Genetic Health Queensland",
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                    {
                        "name": "Rare Disease",
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                    }
                ],
                "child_panel_ids": []
            },
            "transcript": null
        },
        {
            "gene_data": {
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                    "FLJ20510",
                    "PYPAF2",
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                "hgnc_id": "HGNC:22948",
                "gene_name": "NLR family pyrin domain containing 2",
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                    "609364"
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                "Genomics England PanelApp"
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                "version_created": "2026-04-01T10:17:12.005431+11:00",
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                "stats": {
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                        "name": "Genetic Health Queensland",
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                ],
                "child_panel_ids": []
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            "transcript": null
        },
        {
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                    "MATER",
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                "gene_name": "NLR family pyrin domain containing 5",
                "omim_gene": [
                    "609658"
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                "alias_name": [
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                "IUGR"
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            "mode_of_inheritance": "Other",
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                "description": "This panel contains genes associated with growth failure in infancy/early childhood, either isolated or as part of another disorder.\r\n\r\nConsider applying this panel in individuals with:\r\n -Height Standard Deviation Score (SDS) <-3 (very significant short stature - well below the 0.4th centile)\r\nAND at least one of:\r\n- History of small for gestational age (birth weight and/or length <-2SDS)\r\n- Body disproportion, e.g. discrepancy between stature and head size\r\n- Dysmorphic features and congenital anomalies\r\n- Abnormalities in the GH-IGF axis (evidence of GH insensitivity or deficiency) and/or other pituitary hormonal deficiencies\r\n- Family history of significant short stature (1st and 2nd degree relatives) and/or consanguinity\r\n\r\nPrior to genomic testing consider:\r\n-Chromosomal microarray analysis (e.g. Turner syndrome)\r\n-Methylation analysis for Russell-Silver syndrome and Temple syndrome\r\n-Skeletal survey\r\n\r\nAcquired causes of short stature are relatively common.\r\n\r\nDepending on the specific clinical features present, consider applying the Skeletal dysplasia, Intellectual Disability, and/or Pituitary Hormone deficiency panels.\r\n\r\nWith thanks to Genomics England for the original design of this panel.",
                "status": "public",
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                "version_created": "2026-04-01T10:17:12.005431+11:00",
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                    }
                ],
                "child_panel_ids": []
            },
            "transcript": null
        },
        {
            "gene_data": {
                "alias": [
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                "biotype": "protein_coding",
                "hgnc_id": "HGNC:319",
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                "omim_gene": [
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                ],
                "alias_name": [
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                "gene_symbol": "ACAN",
                "hgnc_symbol": "ACAN",
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                "hgnc_date_symbol_changed": "2007-02-16"
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            "entity_type": "gene",
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            "publications": [
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                "19110214",
                "30124491",
                "28331218",
                "20137779"
            ],
            "evidence": [
                "Expert Review Green",
                "Genomics England PanelApp"
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            ],
            "mode_of_inheritance": "BOTH monoallelic and biallelic (but BIALLELIC mutations cause a more SEVERE disease form), autosomal or pseudoautosomal",
            "tags": [],
            "panel": {
                "id": 3631,
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                "description": "This panel contains genes associated with growth failure in infancy/early childhood, either isolated or as part of another disorder.\r\n\r\nConsider applying this panel in individuals with:\r\n -Height Standard Deviation Score (SDS) <-3 (very significant short stature - well below the 0.4th centile)\r\nAND at least one of:\r\n- History of small for gestational age (birth weight and/or length <-2SDS)\r\n- Body disproportion, e.g. discrepancy between stature and head size\r\n- Dysmorphic features and congenital anomalies\r\n- Abnormalities in the GH-IGF axis (evidence of GH insensitivity or deficiency) and/or other pituitary hormonal deficiencies\r\n- Family history of significant short stature (1st and 2nd degree relatives) and/or consanguinity\r\n\r\nPrior to genomic testing consider:\r\n-Chromosomal microarray analysis (e.g. Turner syndrome)\r\n-Methylation analysis for Russell-Silver syndrome and Temple syndrome\r\n-Skeletal survey\r\n\r\nAcquired causes of short stature are relatively common.\r\n\r\nDepending on the specific clinical features present, consider applying the Skeletal dysplasia, Intellectual Disability, and/or Pituitary Hormone deficiency panels.\r\n\r\nWith thanks to Genomics England for the original design of this panel.",
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                    }
                ],
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            },
            "transcript": null
        },
        {
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                "omim_gene": [
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                ],
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            "mode_of_inheritance": "Other",
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                "description": "This panel contains genes associated with growth failure in infancy/early childhood, either isolated or as part of another disorder.\r\n\r\nConsider applying this panel in individuals with:\r\n -Height Standard Deviation Score (SDS) <-3 (very significant short stature - well below the 0.4th centile)\r\nAND at least one of:\r\n- History of small for gestational age (birth weight and/or length <-2SDS)\r\n- Body disproportion, e.g. discrepancy between stature and head size\r\n- Dysmorphic features and congenital anomalies\r\n- Abnormalities in the GH-IGF axis (evidence of GH insensitivity or deficiency) and/or other pituitary hormonal deficiencies\r\n- Family history of significant short stature (1st and 2nd degree relatives) and/or consanguinity\r\n\r\nPrior to genomic testing consider:\r\n-Chromosomal microarray analysis (e.g. Turner syndrome)\r\n-Methylation analysis for Russell-Silver syndrome and Temple syndrome\r\n-Skeletal survey\r\n\r\nAcquired causes of short stature are relatively common.\r\n\r\nDepending on the specific clinical features present, consider applying the Skeletal dysplasia, Intellectual Disability, and/or Pituitary Hormone deficiency panels.\r\n\r\nWith thanks to Genomics England for the original design of this panel.",
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                ],
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            "transcript": null
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        {
            "gene_data": {
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        {
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                },
                "hgnc_date_symbol_changed": "2004-01-28"
            },
            "entity_type": "gene",
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                "25320347",
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            ],
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            "phenotypes": [
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                "Microcephaly and chorioretinopathy, autosomal recessive, 2, #MIM:616171"
            ],
            "mode_of_inheritance": "BIALLELIC, autosomal or pseudoautosomal",
            "tags": [],
            "panel": {
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                "hash_id": null,
                "name": "Growth failure",
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                "disease_sub_group": "",
                "description": "This panel contains genes associated with growth failure in infancy/early childhood, either isolated or as part of another disorder.\r\n\r\nConsider applying this panel in individuals with:\r\n -Height Standard Deviation Score (SDS) <-3 (very significant short stature - well below the 0.4th centile)\r\nAND at least one of:\r\n- History of small for gestational age (birth weight and/or length <-2SDS)\r\n- Body disproportion, e.g. discrepancy between stature and head size\r\n- Dysmorphic features and congenital anomalies\r\n- Abnormalities in the GH-IGF axis (evidence of GH insensitivity or deficiency) and/or other pituitary hormonal deficiencies\r\n- Family history of significant short stature (1st and 2nd degree relatives) and/or consanguinity\r\n\r\nPrior to genomic testing consider:\r\n-Chromosomal microarray analysis (e.g. Turner syndrome)\r\n-Methylation analysis for Russell-Silver syndrome and Temple syndrome\r\n-Skeletal survey\r\n\r\nAcquired causes of short stature are relatively common.\r\n\r\nDepending on the specific clinical features present, consider applying the Skeletal dysplasia, Intellectual Disability, and/or Pituitary Hormone deficiency panels.\r\n\r\nWith thanks to Genomics England for the original design of this panel.",
                "status": "public",
                "version": "1.102",
                "version_created": "2026-04-01T10:17:12.005431+11:00",
                "relevant_disorders": [
                    "Failure to thrive",
                    "HP:0001508; Growth delay",
                    "HP:0001510"
                ],
                "stats": {
                    "number_of_genes": 204,
                    "number_of_strs": 0,
                    "number_of_regions": 4
                },
                "types": [
                    {
                        "name": "Victorian Clinical Genetics Services",
                        "slug": "victorian-clinical-genetics-services",
                        "description": "Panel used by VCGS."
                    },
                    {
                        "name": "Genetic Health Queensland",
                        "slug": "genetic-health-queensland",
                        "description": "Panel used by GHQ."
                    },
                    {
                        "name": "Royal Melbourne Hospital",
                        "slug": "royal-melbourne-hospital",
                        "description": "Royal Melbourne Hospital"
                    },
                    {
                        "name": "Rare Disease",
                        "slug": "rare-disease",
                        "description": "Rare disease panels"
                    }
                ],
                "child_panel_ids": []
            },
            "transcript": null
        },
        {
            "gene_data": {
                "alias": [
                    "K-REV",
                    "RAL1B",
                    "DKFZp586H0723"
                ],
                "biotype": "protein_coding",
                "hgnc_id": "HGNC:9857",
                "gene_name": "RAP1B, member of RAS oncogene family",
                "omim_gene": [
                    "179530"
                ],
                "alias_name": null,
                "gene_symbol": "RAP1B",
                "hgnc_symbol": "RAP1B",
                "hgnc_release": "2017-11-03",
                "ensembl_genes": {
                    "GRch37": {
                        "82": {
                            "location": "12:69004619-69054372",
                            "ensembl_id": "ENSG00000127314"
                        }
                    },
                    "GRch38": {
                        "90": {
                            "location": "12:68610839-68671901",
                            "ensembl_id": "ENSG00000127314"
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                    }
                },
                "hgnc_date_symbol_changed": "1989-06-30"
            },
            "entity_type": "gene",
            "entity_name": "RAP1B",
            "confidence_level": "2",
            "penetrance": null,
            "mode_of_pathogenicity": "",
            "publications": [
                "26280580",
                "32627184"
            ],
            "evidence": [
                "Expert Review Amber",
                "Genomics England PanelApp"
            ],
            "phenotypes": [
                "Thrombocytopenia 1 with multiple congenital anomalies and dysmorphic facies, MIM# 620654"
            ],
            "mode_of_inheritance": "MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown",
            "tags": [],
            "panel": {
                "id": 3631,
                "hash_id": null,
                "name": "Growth failure",
                "disease_group": "",
                "disease_sub_group": "",
                "description": "This panel contains genes associated with growth failure in infancy/early childhood, either isolated or as part of another disorder.\r\n\r\nConsider applying this panel in individuals with:\r\n -Height Standard Deviation Score (SDS) <-3 (very significant short stature - well below the 0.4th centile)\r\nAND at least one of:\r\n- History of small for gestational age (birth weight and/or length <-2SDS)\r\n- Body disproportion, e.g. discrepancy between stature and head size\r\n- Dysmorphic features and congenital anomalies\r\n- Abnormalities in the GH-IGF axis (evidence of GH insensitivity or deficiency) and/or other pituitary hormonal deficiencies\r\n- Family history of significant short stature (1st and 2nd degree relatives) and/or consanguinity\r\n\r\nPrior to genomic testing consider:\r\n-Chromosomal microarray analysis (e.g. Turner syndrome)\r\n-Methylation analysis for Russell-Silver syndrome and Temple syndrome\r\n-Skeletal survey\r\n\r\nAcquired causes of short stature are relatively common.\r\n\r\nDepending on the specific clinical features present, consider applying the Skeletal dysplasia, Intellectual Disability, and/or Pituitary Hormone deficiency panels.\r\n\r\nWith thanks to Genomics England for the original design of this panel.",
                "status": "public",
                "version": "1.102",
                "version_created": "2026-04-01T10:17:12.005431+11:00",
                "relevant_disorders": [
                    "Failure to thrive",
                    "HP:0001508; Growth delay",
                    "HP:0001510"
                ],
                "stats": {
                    "number_of_genes": 204,
                    "number_of_strs": 0,
                    "number_of_regions": 4
                },
                "types": [
                    {
                        "name": "Victorian Clinical Genetics Services",
                        "slug": "victorian-clinical-genetics-services",
                        "description": "Panel used by VCGS."
                    },
                    {
                        "name": "Genetic Health Queensland",
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                        "description": "Panel used by GHQ."
                    },
                    {
                        "name": "Royal Melbourne Hospital",
                        "slug": "royal-melbourne-hospital",
                        "description": "Royal Melbourne Hospital"
                    },
                    {
                        "name": "Rare Disease",
                        "slug": "rare-disease",
                        "description": "Rare disease panels"
                    }
                ],
                "child_panel_ids": []
            },
            "transcript": null
        },
        {
            "gene_data": {
                "alias": [
                    "KIAA1839",
                    "FLJ20008",
                    "RBM40",
                    "SNRNP65"
                ],
                "biotype": "protein_coding",
                "hgnc_id": "HGNC:18666",
                "gene_name": "RNA binding region (RNP1, RRM) containing 3",
                "omim_gene": null,
                "alias_name": [
                    "U11/U12 snRNP 65K"
                ],
                "gene_symbol": "RNPC3",
                "hgnc_symbol": "RNPC3",
                "hgnc_release": "2017-11-03",
                "ensembl_genes": {
                    "GRch37": {
                        "82": {
                            "location": "1:104068313-104097861",
                            "ensembl_id": "ENSG00000185946"
                        }
                    },
                    "GRch38": {
                        "90": {
                            "location": "1:103525691-103555239",
                            "ensembl_id": "ENSG00000185946"
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                    }
                },
                "hgnc_date_symbol_changed": "2002-09-17"
            },
            "entity_type": "gene",
            "entity_name": "RNPC3",
            "confidence_level": "3",
            "penetrance": null,
            "mode_of_pathogenicity": "",
            "publications": [
                "32462814",
                "29866761",
                "24480542",
                "33650182",
                "37463572",
                "35792517",
                "34906446"
            ],
            "evidence": [
                "Expert Review Green",
                "Genomics England PanelApp"
            ],
            "phenotypes": [
                "Growth hormone deficiency",
                "Intellectual disability"
            ],
            "mode_of_inheritance": "BIALLELIC, autosomal or pseudoautosomal",
            "tags": [],
            "panel": {
                "id": 3631,
                "hash_id": null,
                "name": "Growth failure",
                "disease_group": "",
                "disease_sub_group": "",
                "description": "This panel contains genes associated with growth failure in infancy/early childhood, either isolated or as part of another disorder.\r\n\r\nConsider applying this panel in individuals with:\r\n -Height Standard Deviation Score (SDS) <-3 (very significant short stature - well below the 0.4th centile)\r\nAND at least one of:\r\n- History of small for gestational age (birth weight and/or length <-2SDS)\r\n- Body disproportion, e.g. discrepancy between stature and head size\r\n- Dysmorphic features and congenital anomalies\r\n- Abnormalities in the GH-IGF axis (evidence of GH insensitivity or deficiency) and/or other pituitary hormonal deficiencies\r\n- Family history of significant short stature (1st and 2nd degree relatives) and/or consanguinity\r\n\r\nPrior to genomic testing consider:\r\n-Chromosomal microarray analysis (e.g. Turner syndrome)\r\n-Methylation analysis for Russell-Silver syndrome and Temple syndrome\r\n-Skeletal survey\r\n\r\nAcquired causes of short stature are relatively common.\r\n\r\nDepending on the specific clinical features present, consider applying the Skeletal dysplasia, Intellectual Disability, and/or Pituitary Hormone deficiency panels.\r\n\r\nWith thanks to Genomics England for the original design of this panel.",
                "status": "public",
                "version": "1.102",
                "version_created": "2026-04-01T10:17:12.005431+11:00",
                "relevant_disorders": [
                    "Failure to thrive",
                    "HP:0001508; Growth delay",
                    "HP:0001510"
                ],
                "stats": {
                    "number_of_genes": 204,
                    "number_of_strs": 0,
                    "number_of_regions": 4
                },
                "types": [
                    {
                        "name": "Victorian Clinical Genetics Services",
                        "slug": "victorian-clinical-genetics-services",
                        "description": "Panel used by VCGS."
                    },
                    {
                        "name": "Genetic Health Queensland",
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                    {
                        "name": "Royal Melbourne Hospital",
                        "slug": "royal-melbourne-hospital",
                        "description": "Royal Melbourne Hospital"
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                    {
                        "name": "Rare Disease",
                        "slug": "rare-disease",
                        "description": "Rare disease panels"
                    }
                ],
                "child_panel_ids": []
            },
            "transcript": null
        },
        {
            "gene_data": {
                "alias": [
                    "ZNF698",
                    "bA145L22",
                    "bA145L22.2"
                ],
                "biotype": "protein_coding",
                "hgnc_id": "HGNC:18791",
                "gene_name": "ZFP57 zinc finger protein",
                "omim_gene": [
                    "612192"
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                "alias_name": null,
                "gene_symbol": "ZFP57",
                "hgnc_symbol": "ZFP57",
                "hgnc_release": "2017-11-03",
                "ensembl_genes": {
                    "GRch37": {
                        "82": {
                            "location": "6:29640169-29648887",
                            "ensembl_id": "ENSG00000204644"
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                    },
                    "GRch38": {
                        "90": {
                            "location": "6:29672392-29681110",
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                    }
                },
                "hgnc_date_symbol_changed": "2005-07-20"
            },
            "entity_type": "gene",
            "entity_name": "ZFP57",
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            "mode_of_pathogenicity": "",
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                "18622393"
            ],
            "evidence": [
                "Expert Review Green",
                "Genomics England PanelApp"
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            "phenotypes": [
                "Diabetes mellitus, transient neonatal 1, MIM# 601410"
            ],
            "mode_of_inheritance": "BIALLELIC, autosomal or pseudoautosomal",
            "tags": [],
            "panel": {
                "id": 3631,
                "hash_id": null,
                "name": "Growth failure",
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                "description": "This panel contains genes associated with growth failure in infancy/early childhood, either isolated or as part of another disorder.\r\n\r\nConsider applying this panel in individuals with:\r\n -Height Standard Deviation Score (SDS) <-3 (very significant short stature - well below the 0.4th centile)\r\nAND at least one of:\r\n- History of small for gestational age (birth weight and/or length <-2SDS)\r\n- Body disproportion, e.g. discrepancy between stature and head size\r\n- Dysmorphic features and congenital anomalies\r\n- Abnormalities in the GH-IGF axis (evidence of GH insensitivity or deficiency) and/or other pituitary hormonal deficiencies\r\n- Family history of significant short stature (1st and 2nd degree relatives) and/or consanguinity\r\n\r\nPrior to genomic testing consider:\r\n-Chromosomal microarray analysis (e.g. Turner syndrome)\r\n-Methylation analysis for Russell-Silver syndrome and Temple syndrome\r\n-Skeletal survey\r\n\r\nAcquired causes of short stature are relatively common.\r\n\r\nDepending on the specific clinical features present, consider applying the Skeletal dysplasia, Intellectual Disability, and/or Pituitary Hormone deficiency panels.\r\n\r\nWith thanks to Genomics England for the original design of this panel.",
                "status": "public",
                "version": "1.102",
                "version_created": "2026-04-01T10:17:12.005431+11:00",
                "relevant_disorders": [
                    "Failure to thrive",
                    "HP:0001508; Growth delay",
                    "HP:0001510"
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                "stats": {
                    "number_of_genes": 204,
                    "number_of_strs": 0,
                    "number_of_regions": 4
                },
                "types": [
                    {
                        "name": "Victorian Clinical Genetics Services",
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                    {
                        "name": "Royal Melbourne Hospital",
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                    },
                    {
                        "name": "Rare Disease",
                        "slug": "rare-disease",
                        "description": "Rare disease panels"
                    }
                ],
                "child_panel_ids": []
            },
            "transcript": null
        },
        {
            "gene_data": {
                "alias": [
                    "FLJ12343",
                    "MGC20625",
                    "MGC21482",
                    "MGC26740"
                ],
                "biotype": "protein_coding",
                "hgnc_id": "HGNC:33499",
                "gene_name": "ATR interacting protein",
                "omim_gene": [
                    "606605"
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                "alias_name": null,
                "gene_symbol": "ATRIP",
                "hgnc_symbol": "ATRIP",
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                "ensembl_genes": {
                    "GRch37": {
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                    },
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                "hgnc_date_symbol_changed": "2007-06-20"
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            "entity_type": "gene",
            "entity_name": "ATRIP",
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                "23144622"
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            "evidence": [
                "Expert Review Red",
                "Genomics England PanelApp"
            ],
            "phenotypes": [
                "Seckel-like syndrome"
            ],
            "mode_of_inheritance": "BIALLELIC, autosomal or pseudoautosomal",
            "tags": [],
            "panel": {
                "id": 3631,
                "hash_id": null,
                "name": "Growth failure",
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                "description": "This panel contains genes associated with growth failure in infancy/early childhood, either isolated or as part of another disorder.\r\n\r\nConsider applying this panel in individuals with:\r\n -Height Standard Deviation Score (SDS) <-3 (very significant short stature - well below the 0.4th centile)\r\nAND at least one of:\r\n- History of small for gestational age (birth weight and/or length <-2SDS)\r\n- Body disproportion, e.g. discrepancy between stature and head size\r\n- Dysmorphic features and congenital anomalies\r\n- Abnormalities in the GH-IGF axis (evidence of GH insensitivity or deficiency) and/or other pituitary hormonal deficiencies\r\n- Family history of significant short stature (1st and 2nd degree relatives) and/or consanguinity\r\n\r\nPrior to genomic testing consider:\r\n-Chromosomal microarray analysis (e.g. Turner syndrome)\r\n-Methylation analysis for Russell-Silver syndrome and Temple syndrome\r\n-Skeletal survey\r\n\r\nAcquired causes of short stature are relatively common.\r\n\r\nDepending on the specific clinical features present, consider applying the Skeletal dysplasia, Intellectual Disability, and/or Pituitary Hormone deficiency panels.\r\n\r\nWith thanks to Genomics England for the original design of this panel.",
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                    "HP:0001508; Growth delay",
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                "stats": {
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                    "number_of_regions": 4
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                "types": [
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                    }
                ],
                "child_panel_ids": []
            },
            "transcript": null
        },
        {
            "gene_data": {
                "alias": [
                    "XH2",
                    "XNP"
                ],
                "biotype": "protein_coding",
                "hgnc_id": "HGNC:886",
                "gene_name": "ATRX, chromatin remodeler",
                "omim_gene": [
                    "300032",
                    "300504"
                ],
                "alias_name": [
                    "RAD54 homolog (S. cerevisiae)"
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                "gene_symbol": "ATRX",
                "hgnc_symbol": "ATRX",
                "hgnc_release": "2017-11-03",
                "ensembl_genes": {
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                            "location": "X:76760356-77041702",
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                    },
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                            "ensembl_id": "ENSG00000085224"
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                    }
                },
                "hgnc_date_symbol_changed": "1992-11-27"
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            "entity_type": "gene",
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                "20301622"
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            "evidence": [
                "Expert Review Green",
                "Genomics England PanelApp"
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            "phenotypes": [
                "ATR-X-related syndrome MONDO:0016980"
            ],
            "mode_of_inheritance": "X-LINKED: hemizygous mutation in males, monoallelic mutations in females may cause disease (may be less severe, later onset than males)",
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            "panel": {
                "id": 3631,
                "hash_id": null,
                "name": "Growth failure",
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                "child_panel_ids": []
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        },
        {
            "gene_data": {
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                    "ATK",
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                "biotype": "protein_coding",
                "hgnc_id": "HGNC:1133",
                "gene_name": "Bruton tyrosine kinase",
                "omim_gene": [
                    "300300"
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                "alias_name": [
                    "Bruton's tyrosine kinase"
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                "gene_symbol": "BTK",
                "hgnc_symbol": "BTK",
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                "ensembl_genes": {
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                            "location": "X:100604435-100641183",
                            "ensembl_id": "ENSG00000010671"
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                    },
                    "GRch38": {
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                    }
                },
                "hgnc_date_symbol_changed": "1986-01-01"
            },
            "entity_type": "gene",
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            "mode_of_pathogenicity": "",
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                "8013627",
                "7849697",
                "9554752"
            ],
            "evidence": [
                "Expert Review Green",
                "Genomics England PanelApp"
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            "phenotypes": [
                "Isolated growth hormone deficiency, type III, with agammaglobulinaemia, MIM# 307200"
            ],
            "mode_of_inheritance": "X-LINKED: hemizygous mutation in males, biallelic mutations in females",
            "tags": [],
            "panel": {
                "id": 3631,
                "hash_id": null,
                "name": "Growth failure",
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                "description": "This panel contains genes associated with growth failure in infancy/early childhood, either isolated or as part of another disorder.\r\n\r\nConsider applying this panel in individuals with:\r\n -Height Standard Deviation Score (SDS) <-3 (very significant short stature - well below the 0.4th centile)\r\nAND at least one of:\r\n- History of small for gestational age (birth weight and/or length <-2SDS)\r\n- Body disproportion, e.g. discrepancy between stature and head size\r\n- Dysmorphic features and congenital anomalies\r\n- Abnormalities in the GH-IGF axis (evidence of GH insensitivity or deficiency) and/or other pituitary hormonal deficiencies\r\n- Family history of significant short stature (1st and 2nd degree relatives) and/or consanguinity\r\n\r\nPrior to genomic testing consider:\r\n-Chromosomal microarray analysis (e.g. Turner syndrome)\r\n-Methylation analysis for Russell-Silver syndrome and Temple syndrome\r\n-Skeletal survey\r\n\r\nAcquired causes of short stature are relatively common.\r\n\r\nDepending on the specific clinical features present, consider applying the Skeletal dysplasia, Intellectual Disability, and/or Pituitary Hormone deficiency panels.\r\n\r\nWith thanks to Genomics England for the original design of this panel.",
                "status": "public",
                "version": "1.102",
                "version_created": "2026-04-01T10:17:12.005431+11:00",
                "relevant_disorders": [
                    "Failure to thrive",
                    "HP:0001508; Growth delay",
                    "HP:0001510"
                ],
                "stats": {
                    "number_of_genes": 204,
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                    "number_of_regions": 4
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                "types": [
                    {
                        "name": "Victorian Clinical Genetics Services",
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                        "name": "Genetic Health Queensland",
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                "version_created": "2026-04-01T10:17:12.005431+11:00",
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        {
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            "panel": {
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            "transcript": null
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                "CHARGE syndrome, MIM# 214800"
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            "mode_of_inheritance": "MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted",
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            "panel": {
                "id": 3631,
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                "name": "Growth failure",
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                "description": "This panel contains genes associated with growth failure in infancy/early childhood, either isolated or as part of another disorder.\r\n\r\nConsider applying this panel in individuals with:\r\n -Height Standard Deviation Score (SDS) <-3 (very significant short stature - well below the 0.4th centile)\r\nAND at least one of:\r\n- History of small for gestational age (birth weight and/or length <-2SDS)\r\n- Body disproportion, e.g. discrepancy between stature and head size\r\n- Dysmorphic features and congenital anomalies\r\n- Abnormalities in the GH-IGF axis (evidence of GH insensitivity or deficiency) and/or other pituitary hormonal deficiencies\r\n- Family history of significant short stature (1st and 2nd degree relatives) and/or consanguinity\r\n\r\nPrior to genomic testing consider:\r\n-Chromosomal microarray analysis (e.g. Turner syndrome)\r\n-Methylation analysis for Russell-Silver syndrome and Temple syndrome\r\n-Skeletal survey\r\n\r\nAcquired causes of short stature are relatively common.\r\n\r\nDepending on the specific clinical features present, consider applying the Skeletal dysplasia, Intellectual Disability, and/or Pituitary Hormone deficiency panels.\r\n\r\nWith thanks to Genomics England for the original design of this panel.",
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                ],
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                            "location": "11:71139239-71163914",
                            "ensembl_id": "ENSG00000172893"
                        }
                    },
                    "GRch38": {
                        "90": {
                            "location": "11:71428193-71452868",
                            "ensembl_id": "ENSG00000172893"
                        }
                    }
                },
                "hgnc_date_symbol_changed": "1998-04-27"
            },
            "entity_type": "gene",
            "entity_name": "DHCR7",
            "confidence_level": "3",
            "penetrance": null,
            "mode_of_pathogenicity": "",
            "publications": [],
            "evidence": [
                "Expert Review Green",
                "Genomics England PanelApp"
            ],
            "phenotypes": [
                "Smith-Lemli-Opitz syndrome, MIM#270400"
            ],
            "mode_of_inheritance": "BIALLELIC, autosomal or pseudoautosomal",
            "tags": [],
            "panel": {
                "id": 3631,
                "hash_id": null,
                "name": "Growth failure",
                "disease_group": "",
                "disease_sub_group": "",
                "description": "This panel contains genes associated with growth failure in infancy/early childhood, either isolated or as part of another disorder.\r\n\r\nConsider applying this panel in individuals with:\r\n -Height Standard Deviation Score (SDS) <-3 (very significant short stature - well below the 0.4th centile)\r\nAND at least one of:\r\n- History of small for gestational age (birth weight and/or length <-2SDS)\r\n- Body disproportion, e.g. discrepancy between stature and head size\r\n- Dysmorphic features and congenital anomalies\r\n- Abnormalities in the GH-IGF axis (evidence of GH insensitivity or deficiency) and/or other pituitary hormonal deficiencies\r\n- Family history of significant short stature (1st and 2nd degree relatives) and/or consanguinity\r\n\r\nPrior to genomic testing consider:\r\n-Chromosomal microarray analysis (e.g. Turner syndrome)\r\n-Methylation analysis for Russell-Silver syndrome and Temple syndrome\r\n-Skeletal survey\r\n\r\nAcquired causes of short stature are relatively common.\r\n\r\nDepending on the specific clinical features present, consider applying the Skeletal dysplasia, Intellectual Disability, and/or Pituitary Hormone deficiency panels.\r\n\r\nWith thanks to Genomics England for the original design of this panel.",
                "status": "public",
                "version": "1.102",
                "version_created": "2026-04-01T10:17:12.005431+11:00",
                "relevant_disorders": [
                    "Failure to thrive",
                    "HP:0001508; Growth delay",
                    "HP:0001510"
                ],
                "stats": {
                    "number_of_genes": 204,
                    "number_of_strs": 0,
                    "number_of_regions": 4
                },
                "types": [
                    {
                        "name": "Victorian Clinical Genetics Services",
                        "slug": "victorian-clinical-genetics-services",
                        "description": "Panel used by VCGS."
                    },
                    {
                        "name": "Genetic Health Queensland",
                        "slug": "genetic-health-queensland",
                        "description": "Panel used by GHQ."
                    },
                    {
                        "name": "Royal Melbourne Hospital",
                        "slug": "royal-melbourne-hospital",
                        "description": "Royal Melbourne Hospital"
                    },
                    {
                        "name": "Rare Disease",
                        "slug": "rare-disease",
                        "description": "Rare disease panels"
                    }
                ],
                "child_panel_ids": []
            },
            "transcript": null
        },
        {
            "gene_data": {
                "alias": [
                    "KIAA0083"
                ],
                "biotype": "protein_coding",
                "hgnc_id": "HGNC:2939",
                "gene_name": "DNA replication helicase/nuclease 2",
                "omim_gene": [
                    "601810"
                ],
                "alias_name": null,
                "gene_symbol": "DNA2",
                "hgnc_symbol": "DNA2",
                "hgnc_release": "2017-11-03",
                "ensembl_genes": {
                    "GRch37": {
                        "82": {
                            "location": "10:70173821-70231879",
                            "ensembl_id": "ENSG00000138346"
                        }
                    },
                    "GRch38": {
                        "90": {
                            "location": "10:68414064-68472121",
                            "ensembl_id": "ENSG00000138346"
                        }
                    }
                },
                "hgnc_date_symbol_changed": "2008-01-08"
            },
            "entity_type": "gene",
            "entity_name": "DNA2",
            "confidence_level": "3",
            "penetrance": null,
            "mode_of_pathogenicity": "",
            "publications": [
                "24389050",
                "31045292"
            ],
            "evidence": [
                "Expert Review Green",
                "Genomics England PanelApp"
            ],
            "phenotypes": [
                "Seckel syndrome 8, MIM:615807"
            ],
            "mode_of_inheritance": "BIALLELIC, autosomal or pseudoautosomal",
            "tags": [],
            "panel": {
                "id": 3631,
                "hash_id": null,
                "name": "Growth failure",
                "disease_group": "",
                "disease_sub_group": "",
                "description": "This panel contains genes associated with growth failure in infancy/early childhood, either isolated or as part of another disorder.\r\n\r\nConsider applying this panel in individuals with:\r\n -Height Standard Deviation Score (SDS) <-3 (very significant short stature - well below the 0.4th centile)\r\nAND at least one of:\r\n- History of small for gestational age (birth weight and/or length <-2SDS)\r\n- Body disproportion, e.g. discrepancy between stature and head size\r\n- Dysmorphic features and congenital anomalies\r\n- Abnormalities in the GH-IGF axis (evidence of GH insensitivity or deficiency) and/or other pituitary hormonal deficiencies\r\n- Family history of significant short stature (1st and 2nd degree relatives) and/or consanguinity\r\n\r\nPrior to genomic testing consider:\r\n-Chromosomal microarray analysis (e.g. Turner syndrome)\r\n-Methylation analysis for Russell-Silver syndrome and Temple syndrome\r\n-Skeletal survey\r\n\r\nAcquired causes of short stature are relatively common.\r\n\r\nDepending on the specific clinical features present, consider applying the Skeletal dysplasia, Intellectual Disability, and/or Pituitary Hormone deficiency panels.\r\n\r\nWith thanks to Genomics England for the original design of this panel.",
                "status": "public",
                "version": "1.102",
                "version_created": "2026-04-01T10:17:12.005431+11:00",
                "relevant_disorders": [
                    "Failure to thrive",
                    "HP:0001508; Growth delay",
                    "HP:0001510"
                ],
                "stats": {
                    "number_of_genes": 204,
                    "number_of_strs": 0,
                    "number_of_regions": 4
                },
                "types": [
                    {
                        "name": "Victorian Clinical Genetics Services",
                        "slug": "victorian-clinical-genetics-services",
                        "description": "Panel used by VCGS."
                    },
                    {
                        "name": "Genetic Health Queensland",
                        "slug": "genetic-health-queensland",
                        "description": "Panel used by GHQ."
                    },
                    {
                        "name": "Royal Melbourne Hospital",
                        "slug": "royal-melbourne-hospital",
                        "description": "Royal Melbourne Hospital"
                    },
                    {
                        "name": "Rare Disease",
                        "slug": "rare-disease",
                        "description": "Rare disease panels"
                    }
                ],
                "child_panel_ids": []
            },
            "transcript": null
        },
        {
            "gene_data": {
                "alias": [
                    "p300",
                    "KAT3B"
                ],
                "biotype": "protein_coding",
                "hgnc_id": "HGNC:3373",
                "gene_name": "E1A binding protein p300",
                "omim_gene": [
                    "602700"
                ],
                "alias_name": [
                    "histone acetyltransferase p300"
                ],
                "gene_symbol": "EP300",
                "hgnc_symbol": "EP300",
                "hgnc_release": "2017-11-03",
                "ensembl_genes": {
                    "GRch37": {
                        "82": {
                            "location": "22:41487790-41576081",
                            "ensembl_id": "ENSG00000100393"
                        }
                    },
                    "GRch38": {
                        "90": {
                            "location": "22:41091786-41180079",
                            "ensembl_id": "ENSG00000100393"
                        }
                    }
                },
                "hgnc_date_symbol_changed": "1998-07-31"
            },
            "entity_type": "gene",
            "entity_name": "EP300",
            "confidence_level": "3",
            "penetrance": null,
            "mode_of_pathogenicity": "",
            "publications": [
                "29506490",
                "29460469"
            ],
            "evidence": [
                "Expert Review Green",
                "Genomics England PanelApp"
            ],
            "phenotypes": [
                "Rubinstein-Taybi syndrome 2, MIM# 613684",
                "Menke-Hennekam syndrome , MIM#2 618333"
            ],
            "mode_of_inheritance": "MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted",
            "tags": [],
            "panel": {
                "id": 3631,
                "hash_id": null,
                "name": "Growth failure",
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                "description": "This panel contains genes associated with growth failure in infancy/early childhood, either isolated or as part of another disorder.\r\n\r\nConsider applying this panel in individuals with:\r\n -Height Standard Deviation Score (SDS) <-3 (very significant short stature - well below the 0.4th centile)\r\nAND at least one of:\r\n- History of small for gestational age (birth weight and/or length <-2SDS)\r\n- Body disproportion, e.g. discrepancy between stature and head size\r\n- Dysmorphic features and congenital anomalies\r\n- Abnormalities in the GH-IGF axis (evidence of GH insensitivity or deficiency) and/or other pituitary hormonal deficiencies\r\n- Family history of significant short stature (1st and 2nd degree relatives) and/or consanguinity\r\n\r\nPrior to genomic testing consider:\r\n-Chromosomal microarray analysis (e.g. Turner syndrome)\r\n-Methylation analysis for Russell-Silver syndrome and Temple syndrome\r\n-Skeletal survey\r\n\r\nAcquired causes of short stature are relatively common.\r\n\r\nDepending on the specific clinical features present, consider applying the Skeletal dysplasia, Intellectual Disability, and/or Pituitary Hormone deficiency panels.\r\n\r\nWith thanks to Genomics England for the original design of this panel.",
                "status": "public",
                "version": "1.102",
                "version_created": "2026-04-01T10:17:12.005431+11:00",
                "relevant_disorders": [
                    "Failure to thrive",
                    "HP:0001508; Growth delay",
                    "HP:0001510"
                ],
                "stats": {
                    "number_of_genes": 204,
                    "number_of_strs": 0,
                    "number_of_regions": 4
                },
                "types": [
                    {
                        "name": "Victorian Clinical Genetics Services",
                        "slug": "victorian-clinical-genetics-services",
                        "description": "Panel used by VCGS."
                    },
                    {
                        "name": "Genetic Health Queensland",
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                    {
                        "name": "Royal Melbourne Hospital",
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                        "description": "Royal Melbourne Hospital"
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                    {
                        "name": "Rare Disease",
                        "slug": "rare-disease",
                        "description": "Rare disease panels"
                    }
                ],
                "child_panel_ids": []
            },
            "transcript": null
        },
        {
            "gene_data": {
                "alias": [
                    "FLJ20274",
                    "Tan1"
                ],
                "biotype": "protein_coding",
                "hgnc_id": "HGNC:23807",
                "gene_name": "THUMP domain containing 1",
                "omim_gene": [
                    "616662"
                ],
                "alias_name": null,
                "gene_symbol": "THUMPD1",
                "hgnc_symbol": "THUMPD1",
                "hgnc_release": "2017-11-03",
                "ensembl_genes": {
                    "GRch37": {
                        "82": {
                            "location": "16:20744986-20753406",
                            "ensembl_id": "ENSG00000066654"
                        }
                    },
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                            "location": "16:20702816-20742084",
                            "ensembl_id": "ENSG00000066654"
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                    }
                },
                "hgnc_date_symbol_changed": "2004-06-04"
            },
            "entity_type": "gene",
            "entity_name": "THUMPD1",
            "confidence_level": "3",
            "penetrance": null,
            "mode_of_pathogenicity": null,
            "publications": [],
            "evidence": [
                "Expert Review Green",
                "Other"
            ],
            "phenotypes": [
                "Syndromic disease, MONDO:0002254, THUMPD1-related"
            ],
            "mode_of_inheritance": "BIALLELIC, autosomal or pseudoautosomal",
            "tags": [],
            "panel": {
                "id": 3631,
                "hash_id": null,
                "name": "Growth failure",
                "disease_group": "",
                "disease_sub_group": "",
                "description": "This panel contains genes associated with growth failure in infancy/early childhood, either isolated or as part of another disorder.\r\n\r\nConsider applying this panel in individuals with:\r\n -Height Standard Deviation Score (SDS) <-3 (very significant short stature - well below the 0.4th centile)\r\nAND at least one of:\r\n- History of small for gestational age (birth weight and/or length <-2SDS)\r\n- Body disproportion, e.g. discrepancy between stature and head size\r\n- Dysmorphic features and congenital anomalies\r\n- Abnormalities in the GH-IGF axis (evidence of GH insensitivity or deficiency) and/or other pituitary hormonal deficiencies\r\n- Family history of significant short stature (1st and 2nd degree relatives) and/or consanguinity\r\n\r\nPrior to genomic testing consider:\r\n-Chromosomal microarray analysis (e.g. Turner syndrome)\r\n-Methylation analysis for Russell-Silver syndrome and Temple syndrome\r\n-Skeletal survey\r\n\r\nAcquired causes of short stature are relatively common.\r\n\r\nDepending on the specific clinical features present, consider applying the Skeletal dysplasia, Intellectual Disability, and/or Pituitary Hormone deficiency panels.\r\n\r\nWith thanks to Genomics England for the original design of this panel.",
                "status": "public",
                "version": "1.102",
                "version_created": "2026-04-01T10:17:12.005431+11:00",
                "relevant_disorders": [
                    "Failure to thrive",
                    "HP:0001508; Growth delay",
                    "HP:0001510"
                ],
                "stats": {
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                    "number_of_strs": 0,
                    "number_of_regions": 4
                },
                "types": [
                    {
                        "name": "Victorian Clinical Genetics Services",
                        "slug": "victorian-clinical-genetics-services",
                        "description": "Panel used by VCGS."
                    },
                    {
                        "name": "Genetic Health Queensland",
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                    {
                        "name": "Royal Melbourne Hospital",
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                    },
                    {
                        "name": "Rare Disease",
                        "slug": "rare-disease",
                        "description": "Rare disease panels"
                    }
                ],
                "child_panel_ids": []
            },
            "transcript": null
        },
        {
            "gene_data": {
                "alias": [
                    "CSB",
                    "RAD26",
                    "ARMD5"
                ],
                "biotype": "protein_coding",
                "hgnc_id": "HGNC:3438",
                "gene_name": "ERCC excision repair 6, chromatin remodeling factor",
                "omim_gene": [
                    "609413"
                ],
                "alias_name": [
                    "Cockayne syndrome B protein"
                ],
                "gene_symbol": "ERCC6",
                "hgnc_symbol": "ERCC6",
                "hgnc_release": "2017-11-03",
                "ensembl_genes": {
                    "GRch37": {
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                            "location": "10:50663414-50747584",
                            "ensembl_id": "ENSG00000225830"
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                    },
                    "GRch38": {
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                            "location": "10:49455368-49539538",
                            "ensembl_id": "ENSG00000225830"
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                    }
                },
                "hgnc_date_symbol_changed": "1989-06-30"
            },
            "entity_type": "gene",
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            "mode_of_pathogenicity": "",
            "publications": [],
            "evidence": [
                "Expert Review Green",
                "Genomics England PanelApp",
                "Victorian Clinical Genetics Services"
            ],
            "phenotypes": [
                "Cerebrooculofacioskeletal syndrome 1, MIM# 214150",
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                "Cockayne syndrome, type B, MIM# 133540",
                "MONDO:0019570"
            ],
            "mode_of_inheritance": "BIALLELIC, autosomal or pseudoautosomal",
            "tags": [],
            "panel": {
                "id": 3631,
                "hash_id": null,
                "name": "Growth failure",
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                "disease_sub_group": "",
                "description": "This panel contains genes associated with growth failure in infancy/early childhood, either isolated or as part of another disorder.\r\n\r\nConsider applying this panel in individuals with:\r\n -Height Standard Deviation Score (SDS) <-3 (very significant short stature - well below the 0.4th centile)\r\nAND at least one of:\r\n- History of small for gestational age (birth weight and/or length <-2SDS)\r\n- Body disproportion, e.g. discrepancy between stature and head size\r\n- Dysmorphic features and congenital anomalies\r\n- Abnormalities in the GH-IGF axis (evidence of GH insensitivity or deficiency) and/or other pituitary hormonal deficiencies\r\n- Family history of significant short stature (1st and 2nd degree relatives) and/or consanguinity\r\n\r\nPrior to genomic testing consider:\r\n-Chromosomal microarray analysis (e.g. Turner syndrome)\r\n-Methylation analysis for Russell-Silver syndrome and Temple syndrome\r\n-Skeletal survey\r\n\r\nAcquired causes of short stature are relatively common.\r\n\r\nDepending on the specific clinical features present, consider applying the Skeletal dysplasia, Intellectual Disability, and/or Pituitary Hormone deficiency panels.\r\n\r\nWith thanks to Genomics England for the original design of this panel.",
                "status": "public",
                "version": "1.102",
                "version_created": "2026-04-01T10:17:12.005431+11:00",
                "relevant_disorders": [
                    "Failure to thrive",
                    "HP:0001508; Growth delay",
                    "HP:0001510"
                ],
                "stats": {
                    "number_of_genes": 204,
                    "number_of_strs": 0,
                    "number_of_regions": 4
                },
                "types": [
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                        "name": "Victorian Clinical Genetics Services",
                        "slug": "victorian-clinical-genetics-services",
                        "description": "Panel used by VCGS."
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                    {
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                        "name": "Rare Disease",
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                    }
                ],
                "child_panel_ids": []
            },
            "transcript": null
        },
        {
            "gene_data": {
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                    "LZ16",
                    "T13"
                ],
                "biotype": "protein_coding",
                "hgnc_id": "HGNC:21316",
                "gene_name": "ankyrin repeat domain 11",
                "omim_gene": [
                    "611192"
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                "alias_name": null,
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                "hgnc_symbol": "ANKRD11",
                "hgnc_release": "2017-11-03",
                "ensembl_genes": {
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                            "location": "16:89334038-89556969",
                            "ensembl_id": "ENSG00000167522"
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                            "ensembl_id": "ENSG00000167522"
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                    }
                },
                "hgnc_date_symbol_changed": "2004-01-15"
            },
            "entity_type": "gene",
            "entity_name": "ANKRD11",
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            "mode_of_pathogenicity": "",
            "publications": [
                "21782149",
                "33955014",
                "32258089",
                "32124548",
                "31191201",
                "29565525",
                "28449295"
            ],
            "evidence": [
                "Expert Review Green",
                "Genomics England PanelApp"
            ],
            "phenotypes": [
                "KBG syndrome, MIM# 148050"
            ],
            "mode_of_inheritance": "MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted",
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            "panel": {
                "id": 3631,
                "hash_id": null,
                "name": "Growth failure",
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                "description": "This panel contains genes associated with growth failure in infancy/early childhood, either isolated or as part of another disorder.\r\n\r\nConsider applying this panel in individuals with:\r\n -Height Standard Deviation Score (SDS) <-3 (very significant short stature - well below the 0.4th centile)\r\nAND at least one of:\r\n- History of small for gestational age (birth weight and/or length <-2SDS)\r\n- Body disproportion, e.g. discrepancy between stature and head size\r\n- Dysmorphic features and congenital anomalies\r\n- Abnormalities in the GH-IGF axis (evidence of GH insensitivity or deficiency) and/or other pituitary hormonal deficiencies\r\n- Family history of significant short stature (1st and 2nd degree relatives) and/or consanguinity\r\n\r\nPrior to genomic testing consider:\r\n-Chromosomal microarray analysis (e.g. Turner syndrome)\r\n-Methylation analysis for Russell-Silver syndrome and Temple syndrome\r\n-Skeletal survey\r\n\r\nAcquired causes of short stature are relatively common.\r\n\r\nDepending on the specific clinical features present, consider applying the Skeletal dysplasia, Intellectual Disability, and/or Pituitary Hormone deficiency panels.\r\n\r\nWith thanks to Genomics England for the original design of this panel.",
                "status": "public",
                "version": "1.102",
                "version_created": "2026-04-01T10:17:12.005431+11:00",
                "relevant_disorders": [
                    "Failure to thrive",
                    "HP:0001508; Growth delay",
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                "stats": {
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                    "number_of_strs": 0,
                    "number_of_regions": 4
                },
                "types": [
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                        "description": "Panel used by VCGS."
                    },
                    {
                        "name": "Genetic Health Queensland",
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                    {
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                    {
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                    }
                ],
                "child_panel_ids": []
            },
            "transcript": null
        },
        {
            "gene_data": {
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                    "CSA"
                ],
                "biotype": "protein_coding",
                "hgnc_id": "HGNC:3439",
                "gene_name": "ERCC excision repair 8, CSA ubiquitin ligase complex subunit",
                "omim_gene": [
                    "609412"
                ],
                "alias_name": null,
                "gene_symbol": "ERCC8",
                "hgnc_symbol": "ERCC8",
                "hgnc_release": "2017-11-03",
                "ensembl_genes": {
                    "GRch37": {
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                            "location": "5:60169658-60240900",
                            "ensembl_id": "ENSG00000049167"
                        }
                    },
                    "GRch38": {
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                            "location": "5:60873831-60945073",
                            "ensembl_id": "ENSG00000049167"
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                    }
                },
                "hgnc_date_symbol_changed": "1995-02-07"
            },
            "entity_type": "gene",
            "entity_name": "ERCC8",
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            "mode_of_pathogenicity": "",
            "publications": [
                "7664335",
                "19894250"
            ],
            "evidence": [
                "Expert Review Green",
                "Genomics England PanelApp",
                "Victorian Clinical Genetics Services"
            ],
            "phenotypes": [
                "Cockayne syndrome, type A, MIM# 216400",
                "MONDO:0019569"
            ],
            "mode_of_inheritance": "BIALLELIC, autosomal or pseudoautosomal",
            "tags": [],
            "panel": {
                "id": 3631,
                "hash_id": null,
                "name": "Growth failure",
                "disease_group": "",
                "disease_sub_group": "",
                "description": "This panel contains genes associated with growth failure in infancy/early childhood, either isolated or as part of another disorder.\r\n\r\nConsider applying this panel in individuals with:\r\n -Height Standard Deviation Score (SDS) <-3 (very significant short stature - well below the 0.4th centile)\r\nAND at least one of:\r\n- History of small for gestational age (birth weight and/or length <-2SDS)\r\n- Body disproportion, e.g. discrepancy between stature and head size\r\n- Dysmorphic features and congenital anomalies\r\n- Abnormalities in the GH-IGF axis (evidence of GH insensitivity or deficiency) and/or other pituitary hormonal deficiencies\r\n- Family history of significant short stature (1st and 2nd degree relatives) and/or consanguinity\r\n\r\nPrior to genomic testing consider:\r\n-Chromosomal microarray analysis (e.g. Turner syndrome)\r\n-Methylation analysis for Russell-Silver syndrome and Temple syndrome\r\n-Skeletal survey\r\n\r\nAcquired causes of short stature are relatively common.\r\n\r\nDepending on the specific clinical features present, consider applying the Skeletal dysplasia, Intellectual Disability, and/or Pituitary Hormone deficiency panels.\r\n\r\nWith thanks to Genomics England for the original design of this panel.",
                "status": "public",
                "version": "1.102",
                "version_created": "2026-04-01T10:17:12.005431+11:00",
                "relevant_disorders": [
                    "Failure to thrive",
                    "HP:0001508; Growth delay",
                    "HP:0001510"
                ],
                "stats": {
                    "number_of_genes": 204,
                    "number_of_strs": 0,
                    "number_of_regions": 4
                },
                "types": [
                    {
                        "name": "Victorian Clinical Genetics Services",
                        "slug": "victorian-clinical-genetics-services",
                        "description": "Panel used by VCGS."
                    },
                    {
                        "name": "Genetic Health Queensland",
                        "slug": "genetic-health-queensland",
                        "description": "Panel used by GHQ."
                    },
                    {
                        "name": "Royal Melbourne Hospital",
                        "slug": "royal-melbourne-hospital",
                        "description": "Royal Melbourne Hospital"
                    },
                    {
                        "name": "Rare Disease",
                        "slug": "rare-disease",
                        "description": "Rare disease panels"
                    }
                ],
                "child_panel_ids": []
            },
            "transcript": null
        }
    ]
}