Search Genes

GET /api/v1/genes/?format=api&page=171
HTTP 200 OK
Allow: GET, HEAD, OPTIONS
Content-Type: application/json
Vary: Accept

{
    "count": 35560,
    "next": "https://panelapp-aus.org/api/v1/genes/?format=api&page=172",
    "previous": "https://panelapp-aus.org/api/v1/genes/?format=api&page=170",
    "results": [
        {
            "gene_data": {
                "alias": [
                    "IL1F2",
                    "IL-1B",
                    "IL1-BETA"
                ],
                "biotype": "protein_coding",
                "hgnc_id": "HGNC:5992",
                "gene_name": "interleukin 1 beta",
                "omim_gene": [
                    "147720"
                ],
                "alias_name": null,
                "gene_symbol": "IL1B",
                "hgnc_symbol": "IL1B",
                "hgnc_release": "2017-11-03",
                "ensembl_genes": {
                    "GRch37": {
                        "82": {
                            "location": "2:113587328-113594480",
                            "ensembl_id": "ENSG00000125538"
                        }
                    },
                    "GRch38": {
                        "90": {
                            "location": "2:112829751-112836903",
                            "ensembl_id": "ENSG00000125538"
                        }
                    }
                },
                "hgnc_date_symbol_changed": "1989-03-31"
            },
            "entity_type": "gene",
            "entity_name": "IL1B",
            "confidence_level": "3",
            "penetrance": null,
            "mode_of_pathogenicity": "",
            "publications": [],
            "evidence": [
                "Expert list",
                "Expert Review Green"
            ],
            "phenotypes": [],
            "mode_of_inheritance": "Unknown",
            "tags": [
                "umccr"
            ],
            "panel": {
                "id": 243,
                "hash_id": null,
                "name": "Immune_markers_WTS_UMCCR",
                "disease_group": "Cancer",
                "disease_sub_group": "",
                "description": "Author: Jacek Marzec, jacek.marzec@unimelb.edu.au\r\n\r\nPurpose: panel of immune markers used to assess pre-existing anti-cancer immunity and likelihood of response to immunotherapy. This set of genes is used in UMCCR WTS report \"Immune markers\" section\r\n\r\nSource: https://www.omniseq.com\r\n\r\nGithub: https://github.com/umccr/RNAsum",
                "status": "public",
                "version": "0.77",
                "version_created": "2025-11-03T15:30:48.145923+11:00",
                "relevant_disorders": [],
                "stats": {
                    "number_of_genes": 71,
                    "number_of_strs": 0,
                    "number_of_regions": 0
                },
                "types": [],
                "child_panel_ids": []
            },
            "transcript": null
        },
        {
            "gene_data": {
                "alias": [
                    "CSIF",
                    "TGIF",
                    "IL10A",
                    "IL-10"
                ],
                "biotype": "protein_coding",
                "hgnc_id": "HGNC:5962",
                "gene_name": "interleukin 10",
                "omim_gene": [
                    "124092"
                ],
                "alias_name": [
                    "cytokine synthesis inhibitory factor",
                    "T-cell growth inhibitory factor"
                ],
                "gene_symbol": "IL10",
                "hgnc_symbol": "IL10",
                "hgnc_release": "2017-11-03",
                "ensembl_genes": {
                    "GRch37": {
                        "82": {
                            "location": "1:206940947-206945839",
                            "ensembl_id": "ENSG00000136634"
                        }
                    },
                    "GRch38": {
                        "90": {
                            "location": "1:206767602-206772494",
                            "ensembl_id": "ENSG00000136634"
                        }
                    }
                },
                "hgnc_date_symbol_changed": "1991-10-31"
            },
            "entity_type": "gene",
            "entity_name": "IL10",
            "confidence_level": "3",
            "penetrance": null,
            "mode_of_pathogenicity": "",
            "publications": [],
            "evidence": [
                "Expert list",
                "Expert Review Green"
            ],
            "phenotypes": [],
            "mode_of_inheritance": "Unknown",
            "tags": [
                "umccr"
            ],
            "panel": {
                "id": 243,
                "hash_id": null,
                "name": "Immune_markers_WTS_UMCCR",
                "disease_group": "Cancer",
                "disease_sub_group": "",
                "description": "Author: Jacek Marzec, jacek.marzec@unimelb.edu.au\r\n\r\nPurpose: panel of immune markers used to assess pre-existing anti-cancer immunity and likelihood of response to immunotherapy. This set of genes is used in UMCCR WTS report \"Immune markers\" section\r\n\r\nSource: https://www.omniseq.com\r\n\r\nGithub: https://github.com/umccr/RNAsum",
                "status": "public",
                "version": "0.77",
                "version_created": "2025-11-03T15:30:48.145923+11:00",
                "relevant_disorders": [],
                "stats": {
                    "number_of_genes": 71,
                    "number_of_strs": 0,
                    "number_of_regions": 0
                },
                "types": [],
                "child_panel_ids": []
            },
            "transcript": null
        },
        {
            "gene_data": {
                "alias": [],
                "biotype": "protein_coding",
                "hgnc_id": "HGNC:5438",
                "gene_name": "interferon gamma",
                "omim_gene": [
                    "147570"
                ],
                "alias_name": null,
                "gene_symbol": "IFNG",
                "hgnc_symbol": "IFNG",
                "hgnc_release": "2017-11-03",
                "ensembl_genes": {
                    "GRch37": {
                        "82": {
                            "location": "12:68548548-68553527",
                            "ensembl_id": "ENSG00000111537"
                        }
                    },
                    "GRch38": {
                        "90": {
                            "location": "12:68154768-68159747",
                            "ensembl_id": "ENSG00000111537"
                        }
                    }
                },
                "hgnc_date_symbol_changed": "1986-01-01"
            },
            "entity_type": "gene",
            "entity_name": "IFNG",
            "confidence_level": "3",
            "penetrance": null,
            "mode_of_pathogenicity": "",
            "publications": [],
            "evidence": [
                "Expert list",
                "Expert Review Green"
            ],
            "phenotypes": [],
            "mode_of_inheritance": "Unknown",
            "tags": [
                "umccr"
            ],
            "panel": {
                "id": 243,
                "hash_id": null,
                "name": "Immune_markers_WTS_UMCCR",
                "disease_group": "Cancer",
                "disease_sub_group": "",
                "description": "Author: Jacek Marzec, jacek.marzec@unimelb.edu.au\r\n\r\nPurpose: panel of immune markers used to assess pre-existing anti-cancer immunity and likelihood of response to immunotherapy. This set of genes is used in UMCCR WTS report \"Immune markers\" section\r\n\r\nSource: https://www.omniseq.com\r\n\r\nGithub: https://github.com/umccr/RNAsum",
                "status": "public",
                "version": "0.77",
                "version_created": "2025-11-03T15:30:48.145923+11:00",
                "relevant_disorders": [],
                "stats": {
                    "number_of_genes": 71,
                    "number_of_strs": 0,
                    "number_of_regions": 0
                },
                "types": [],
                "child_panel_ids": []
            },
            "transcript": null
        },
        {
            "gene_data": {
                "alias": [
                    "KIAA0653",
                    "GL50",
                    "B7-H2",
                    "B7RP-1",
                    "B7H2",
                    "B7RP1",
                    "ICOS-L",
                    "CD275"
                ],
                "biotype": "protein_coding",
                "hgnc_id": "HGNC:17087",
                "gene_name": "inducible T-cell costimulator ligand",
                "omim_gene": [
                    "605717"
                ],
                "alias_name": [
                    "B7-related protein 1",
                    "B7 homologue 2",
                    "B7 homolog 2"
                ],
                "gene_symbol": "ICOSLG",
                "hgnc_symbol": "ICOSLG",
                "hgnc_release": "2017-11-03",
                "ensembl_genes": {
                    "GRch37": {
                        "82": {
                            "location": "21:45642874-45660849",
                            "ensembl_id": "ENSG00000160223"
                        }
                    },
                    "GRch38": {
                        "90": {
                            "location": "21:44222991-44240966",
                            "ensembl_id": "ENSG00000160223"
                        }
                    }
                },
                "hgnc_date_symbol_changed": "2005-01-12"
            },
            "entity_type": "gene",
            "entity_name": "ICOSLG",
            "confidence_level": "3",
            "penetrance": null,
            "mode_of_pathogenicity": "",
            "publications": [],
            "evidence": [
                "Expert list",
                "Expert Review Green"
            ],
            "phenotypes": [],
            "mode_of_inheritance": "Unknown",
            "tags": [
                "umccr"
            ],
            "panel": {
                "id": 243,
                "hash_id": null,
                "name": "Immune_markers_WTS_UMCCR",
                "disease_group": "Cancer",
                "disease_sub_group": "",
                "description": "Author: Jacek Marzec, jacek.marzec@unimelb.edu.au\r\n\r\nPurpose: panel of immune markers used to assess pre-existing anti-cancer immunity and likelihood of response to immunotherapy. This set of genes is used in UMCCR WTS report \"Immune markers\" section\r\n\r\nSource: https://www.omniseq.com\r\n\r\nGithub: https://github.com/umccr/RNAsum",
                "status": "public",
                "version": "0.77",
                "version_created": "2025-11-03T15:30:48.145923+11:00",
                "relevant_disorders": [],
                "stats": {
                    "number_of_genes": 71,
                    "number_of_strs": 0,
                    "number_of_regions": 0
                },
                "types": [],
                "child_panel_ids": []
            },
            "transcript": null
        },
        {
            "gene_data": {
                "alias": [],
                "biotype": "protein_coding",
                "hgnc_id": "HGNC:6059",
                "gene_name": "indoleamine 2,3-dioxygenase 1",
                "omim_gene": [
                    "147435"
                ],
                "alias_name": null,
                "gene_symbol": "IDO1",
                "hgnc_symbol": "IDO1",
                "hgnc_release": "2017-11-03",
                "ensembl_genes": {
                    "GRch37": {
                        "82": {
                            "location": "8:39759794-39785963",
                            "ensembl_id": "ENSG00000131203"
                        }
                    },
                    "GRch38": {
                        "90": {
                            "location": "8:39902275-39928444",
                            "ensembl_id": "ENSG00000131203"
                        }
                    }
                },
                "hgnc_date_symbol_changed": "2009-01-07"
            },
            "entity_type": "gene",
            "entity_name": "IDO1",
            "confidence_level": "3",
            "penetrance": null,
            "mode_of_pathogenicity": "",
            "publications": [],
            "evidence": [
                "Expert list",
                "Expert Review Green"
            ],
            "phenotypes": [],
            "mode_of_inheritance": "Unknown",
            "tags": [
                "umccr"
            ],
            "panel": {
                "id": 243,
                "hash_id": null,
                "name": "Immune_markers_WTS_UMCCR",
                "disease_group": "Cancer",
                "disease_sub_group": "",
                "description": "Author: Jacek Marzec, jacek.marzec@unimelb.edu.au\r\n\r\nPurpose: panel of immune markers used to assess pre-existing anti-cancer immunity and likelihood of response to immunotherapy. This set of genes is used in UMCCR WTS report \"Immune markers\" section\r\n\r\nSource: https://www.omniseq.com\r\n\r\nGithub: https://github.com/umccr/RNAsum",
                "status": "public",
                "version": "0.77",
                "version_created": "2025-11-03T15:30:48.145923+11:00",
                "relevant_disorders": [],
                "stats": {
                    "number_of_genes": 71,
                    "number_of_strs": 0,
                    "number_of_regions": 0
                },
                "types": [],
                "child_panel_ids": []
            },
            "transcript": null
        },
        {
            "gene_data": {
                "alias": [
                    "AILIM",
                    "CD278"
                ],
                "biotype": "protein_coding",
                "hgnc_id": "HGNC:5351",
                "gene_name": "inducible T-cell costimulator",
                "omim_gene": [
                    "604558"
                ],
                "alias_name": [
                    "activation-inducible lymphocyte immunomediatory molecule"
                ],
                "gene_symbol": "ICOS",
                "hgnc_symbol": "ICOS",
                "hgnc_release": "2017-11-03",
                "ensembl_genes": {
                    "GRch37": {
                        "82": {
                            "location": "2:204801471-204826300",
                            "ensembl_id": "ENSG00000163600"
                        }
                    },
                    "GRch38": {
                        "90": {
                            "location": "2:203936748-203961577",
                            "ensembl_id": "ENSG00000163600"
                        }
                    }
                },
                "hgnc_date_symbol_changed": "2000-02-29"
            },
            "entity_type": "gene",
            "entity_name": "ICOS",
            "confidence_level": "3",
            "penetrance": null,
            "mode_of_pathogenicity": "",
            "publications": [],
            "evidence": [
                "Expert list",
                "Expert Review Green"
            ],
            "phenotypes": [],
            "mode_of_inheritance": "Unknown",
            "tags": [
                "umccr"
            ],
            "panel": {
                "id": 243,
                "hash_id": null,
                "name": "Immune_markers_WTS_UMCCR",
                "disease_group": "Cancer",
                "disease_sub_group": "",
                "description": "Author: Jacek Marzec, jacek.marzec@unimelb.edu.au\r\n\r\nPurpose: panel of immune markers used to assess pre-existing anti-cancer immunity and likelihood of response to immunotherapy. This set of genes is used in UMCCR WTS report \"Immune markers\" section\r\n\r\nSource: https://www.omniseq.com\r\n\r\nGithub: https://github.com/umccr/RNAsum",
                "status": "public",
                "version": "0.77",
                "version_created": "2025-11-03T15:30:48.145923+11:00",
                "relevant_disorders": [],
                "stats": {
                    "number_of_genes": 71,
                    "number_of_strs": 0,
                    "number_of_regions": 0
                },
                "types": [],
                "child_panel_ids": []
            },
            "transcript": null
        },
        {
            "gene_data": {
                "alias": [
                    "Tim-3",
                    "TIM3",
                    "FLJ14428",
                    "TIMD3",
                    "CD366"
                ],
                "biotype": "protein_coding",
                "hgnc_id": "HGNC:18437",
                "gene_name": "hepatitis A virus cellular receptor 2",
                "omim_gene": [
                    "606652"
                ],
                "alias_name": [
                    "T-cell immunoglobulin mucin family member 3"
                ],
                "gene_symbol": "HAVCR2",
                "hgnc_symbol": "HAVCR2",
                "hgnc_release": "2017-11-03",
                "ensembl_genes": {
                    "GRch37": {
                        "82": {
                            "location": "5:156512843-156569880",
                            "ensembl_id": "ENSG00000135077"
                        }
                    },
                    "GRch38": {
                        "90": {
                            "location": "5:157085832-157142869",
                            "ensembl_id": "ENSG00000135077"
                        }
                    }
                },
                "hgnc_date_symbol_changed": "2002-12-04"
            },
            "entity_type": "gene",
            "entity_name": "HAVCR2",
            "confidence_level": "3",
            "penetrance": null,
            "mode_of_pathogenicity": "",
            "publications": [],
            "evidence": [
                "Expert list",
                "Expert Review Green"
            ],
            "phenotypes": [],
            "mode_of_inheritance": "Unknown",
            "tags": [
                "umccr"
            ],
            "panel": {
                "id": 243,
                "hash_id": null,
                "name": "Immune_markers_WTS_UMCCR",
                "disease_group": "Cancer",
                "disease_sub_group": "",
                "description": "Author: Jacek Marzec, jacek.marzec@unimelb.edu.au\r\n\r\nPurpose: panel of immune markers used to assess pre-existing anti-cancer immunity and likelihood of response to immunotherapy. This set of genes is used in UMCCR WTS report \"Immune markers\" section\r\n\r\nSource: https://www.omniseq.com\r\n\r\nGithub: https://github.com/umccr/RNAsum",
                "status": "public",
                "version": "0.77",
                "version_created": "2025-11-03T15:30:48.145923+11:00",
                "relevant_disorders": [],
                "stats": {
                    "number_of_genes": 71,
                    "number_of_strs": 0,
                    "number_of_regions": 0
                },
                "types": [],
                "child_panel_ids": []
            },
            "transcript": null
        },
        {
            "gene_data": {
                "alias": [
                    "CCPI",
                    "CGL-1",
                    "CSP-B",
                    "CGL1",
                    "CTSGL1",
                    "HLP",
                    "SECT"
                ],
                "biotype": "protein_coding",
                "hgnc_id": "HGNC:4709",
                "gene_name": "granzyme B",
                "omim_gene": [
                    "123910"
                ],
                "alias_name": [
                    "fragmentin 2",
                    "cytotoxic serine protease B",
                    "cathepsin G-like 1",
                    "T-cell serine protease 1-3E",
                    "granzyme 2",
                    "cytotoxic T-lymphocyte-associated serine esterase 1"
                ],
                "gene_symbol": "GZMB",
                "hgnc_symbol": "GZMB",
                "hgnc_release": "2017-11-03",
                "ensembl_genes": {
                    "GRch37": {
                        "82": {
                            "location": "14:25100160-25103473",
                            "ensembl_id": "ENSG00000100453"
                        }
                    },
                    "GRch38": {
                        "90": {
                            "location": "14:24630954-24634267",
                            "ensembl_id": "ENSG00000100453"
                        }
                    }
                },
                "hgnc_date_symbol_changed": "1989-05-12"
            },
            "entity_type": "gene",
            "entity_name": "GZMB",
            "confidence_level": "3",
            "penetrance": null,
            "mode_of_pathogenicity": "",
            "publications": [],
            "evidence": [
                "Expert list",
                "Expert Review Green"
            ],
            "phenotypes": [],
            "mode_of_inheritance": "Unknown",
            "tags": [
                "umccr"
            ],
            "panel": {
                "id": 243,
                "hash_id": null,
                "name": "Immune_markers_WTS_UMCCR",
                "disease_group": "Cancer",
                "disease_sub_group": "",
                "description": "Author: Jacek Marzec, jacek.marzec@unimelb.edu.au\r\n\r\nPurpose: panel of immune markers used to assess pre-existing anti-cancer immunity and likelihood of response to immunotherapy. This set of genes is used in UMCCR WTS report \"Immune markers\" section\r\n\r\nSource: https://www.omniseq.com\r\n\r\nGithub: https://github.com/umccr/RNAsum",
                "status": "public",
                "version": "0.77",
                "version_created": "2025-11-03T15:30:48.145923+11:00",
                "relevant_disorders": [],
                "stats": {
                    "number_of_genes": 71,
                    "number_of_strs": 0,
                    "number_of_regions": 0
                },
                "types": [],
                "child_panel_ids": []
            },
            "transcript": null
        },
        {
            "gene_data": {
                "alias": [],
                "biotype": "protein_coding",
                "hgnc_id": "HGNC:4708",
                "gene_name": "granzyme A",
                "omim_gene": [
                    "140050"
                ],
                "alias_name": [
                    "CTL tryptase",
                    "Cytotoxic T-lymphocyte-associated serine esterase-3",
                    "Hanukah factor serine protease)",
                    "granzyme 1"
                ],
                "gene_symbol": "GZMA",
                "hgnc_symbol": "GZMA",
                "hgnc_release": "2017-11-03",
                "ensembl_genes": {
                    "GRch37": {
                        "82": {
                            "location": "5:54398476-54406080",
                            "ensembl_id": "ENSG00000145649"
                        }
                    },
                    "GRch38": {
                        "90": {
                            "location": "5:55102648-55110252",
                            "ensembl_id": "ENSG00000145649"
                        }
                    }
                },
                "hgnc_date_symbol_changed": "1988-05-31"
            },
            "entity_type": "gene",
            "entity_name": "GZMA",
            "confidence_level": "3",
            "penetrance": null,
            "mode_of_pathogenicity": "",
            "publications": [],
            "evidence": [
                "Expert list",
                "Expert Review Green"
            ],
            "phenotypes": [],
            "mode_of_inheritance": "Unknown",
            "tags": [
                "umccr"
            ],
            "panel": {
                "id": 243,
                "hash_id": null,
                "name": "Immune_markers_WTS_UMCCR",
                "disease_group": "Cancer",
                "disease_sub_group": "",
                "description": "Author: Jacek Marzec, jacek.marzec@unimelb.edu.au\r\n\r\nPurpose: panel of immune markers used to assess pre-existing anti-cancer immunity and likelihood of response to immunotherapy. This set of genes is used in UMCCR WTS report \"Immune markers\" section\r\n\r\nSource: https://www.omniseq.com\r\n\r\nGithub: https://github.com/umccr/RNAsum",
                "status": "public",
                "version": "0.77",
                "version_created": "2025-11-03T15:30:48.145923+11:00",
                "relevant_disorders": [],
                "stats": {
                    "number_of_genes": 71,
                    "number_of_strs": 0,
                    "number_of_regions": 0
                },
                "types": [],
                "child_panel_ids": []
            },
            "transcript": null
        },
        {
            "gene_data": {
                "alias": [
                    "HDR"
                ],
                "biotype": "protein_coding",
                "hgnc_id": "HGNC:4172",
                "gene_name": "GATA binding protein 3",
                "omim_gene": [
                    "131320"
                ],
                "alias_name": null,
                "gene_symbol": "GATA3",
                "hgnc_symbol": "GATA3",
                "hgnc_release": "2017-11-03",
                "ensembl_genes": {
                    "GRch37": {
                        "82": {
                            "location": "10:8095567-8117161",
                            "ensembl_id": "ENSG00000107485"
                        }
                    },
                    "GRch38": {
                        "90": {
                            "location": "10:8053604-8075198",
                            "ensembl_id": "ENSG00000107485"
                        }
                    }
                },
                "hgnc_date_symbol_changed": "1992-11-03"
            },
            "entity_type": "gene",
            "entity_name": "GATA3",
            "confidence_level": "3",
            "penetrance": null,
            "mode_of_pathogenicity": "",
            "publications": [],
            "evidence": [
                "Expert list",
                "Expert Review Green"
            ],
            "phenotypes": [],
            "mode_of_inheritance": "Unknown",
            "tags": [
                "umccr"
            ],
            "panel": {
                "id": 243,
                "hash_id": null,
                "name": "Immune_markers_WTS_UMCCR",
                "disease_group": "Cancer",
                "disease_sub_group": "",
                "description": "Author: Jacek Marzec, jacek.marzec@unimelb.edu.au\r\n\r\nPurpose: panel of immune markers used to assess pre-existing anti-cancer immunity and likelihood of response to immunotherapy. This set of genes is used in UMCCR WTS report \"Immune markers\" section\r\n\r\nSource: https://www.omniseq.com\r\n\r\nGithub: https://github.com/umccr/RNAsum",
                "status": "public",
                "version": "0.77",
                "version_created": "2025-11-03T15:30:48.145923+11:00",
                "relevant_disorders": [],
                "stats": {
                    "number_of_genes": 71,
                    "number_of_strs": 0,
                    "number_of_regions": 0
                },
                "types": [],
                "child_panel_ids": []
            },
            "transcript": null
        },
        {
            "gene_data": {
                "alias": [
                    "JM2",
                    "XPID",
                    "AIID",
                    "PIDX",
                    "DIETER",
                    "SCURFIN"
                ],
                "biotype": "protein_coding",
                "hgnc_id": "HGNC:6106",
                "gene_name": "forkhead box P3",
                "omim_gene": [
                    "300292"
                ],
                "alias_name": null,
                "gene_symbol": "FOXP3",
                "hgnc_symbol": "FOXP3",
                "hgnc_release": "2017-11-03",
                "ensembl_genes": {
                    "GRch37": {
                        "82": {
                            "location": "X:49106897-49121288",
                            "ensembl_id": "ENSG00000049768"
                        }
                    },
                    "GRch38": {
                        "90": {
                            "location": "X:49250436-49264826",
                            "ensembl_id": "ENSG00000049768"
                        }
                    }
                },
                "hgnc_date_symbol_changed": "2002-09-20"
            },
            "entity_type": "gene",
            "entity_name": "FOXP3",
            "confidence_level": "3",
            "penetrance": null,
            "mode_of_pathogenicity": "",
            "publications": [],
            "evidence": [
                "Expert list",
                "Expert Review Green"
            ],
            "phenotypes": [],
            "mode_of_inheritance": "Unknown",
            "tags": [
                "umccr"
            ],
            "panel": {
                "id": 243,
                "hash_id": null,
                "name": "Immune_markers_WTS_UMCCR",
                "disease_group": "Cancer",
                "disease_sub_group": "",
                "description": "Author: Jacek Marzec, jacek.marzec@unimelb.edu.au\r\n\r\nPurpose: panel of immune markers used to assess pre-existing anti-cancer immunity and likelihood of response to immunotherapy. This set of genes is used in UMCCR WTS report \"Immune markers\" section\r\n\r\nSource: https://www.omniseq.com\r\n\r\nGithub: https://github.com/umccr/RNAsum",
                "status": "public",
                "version": "0.77",
                "version_created": "2025-11-03T15:30:48.145923+11:00",
                "relevant_disorders": [],
                "stats": {
                    "number_of_genes": 71,
                    "number_of_strs": 0,
                    "number_of_regions": 0
                },
                "types": [],
                "child_panel_ids": []
            },
            "transcript": null
        },
        {
            "gene_data": {
                "alias": [
                    "DPPIV"
                ],
                "biotype": "protein_coding",
                "hgnc_id": "HGNC:3590",
                "gene_name": "fibroblast activation protein alpha",
                "omim_gene": [
                    "600403"
                ],
                "alias_name": [
                    "seprase"
                ],
                "gene_symbol": "FAP",
                "hgnc_symbol": "FAP",
                "hgnc_release": "2017-11-03",
                "ensembl_genes": {
                    "GRch37": {
                        "82": {
                            "location": "2:163027194-163101661",
                            "ensembl_id": "ENSG00000078098"
                        }
                    },
                    "GRch38": {
                        "90": {
                            "location": "2:162170684-162245151",
                            "ensembl_id": "ENSG00000078098"
                        }
                    }
                },
                "hgnc_date_symbol_changed": "1995-03-28"
            },
            "entity_type": "gene",
            "entity_name": "FAP",
            "confidence_level": "3",
            "penetrance": null,
            "mode_of_pathogenicity": "",
            "publications": [],
            "evidence": [
                "Expert list",
                "Expert Review Green"
            ],
            "phenotypes": [],
            "mode_of_inheritance": "Unknown",
            "tags": [
                "umccr"
            ],
            "panel": {
                "id": 243,
                "hash_id": null,
                "name": "Immune_markers_WTS_UMCCR",
                "disease_group": "Cancer",
                "disease_sub_group": "",
                "description": "Author: Jacek Marzec, jacek.marzec@unimelb.edu.au\r\n\r\nPurpose: panel of immune markers used to assess pre-existing anti-cancer immunity and likelihood of response to immunotherapy. This set of genes is used in UMCCR WTS report \"Immune markers\" section\r\n\r\nSource: https://www.omniseq.com\r\n\r\nGithub: https://github.com/umccr/RNAsum",
                "status": "public",
                "version": "0.77",
                "version_created": "2025-11-03T15:30:48.145923+11:00",
                "relevant_disorders": [],
                "stats": {
                    "number_of_genes": 71,
                    "number_of_strs": 0,
                    "number_of_regions": 0
                },
                "types": [],
                "child_panel_ids": []
            },
            "transcript": null
        },
        {
            "gene_data": {
                "alias": [],
                "biotype": "protein_coding",
                "hgnc_id": "HGNC:3466",
                "gene_name": "endothelial cell specific molecule 1",
                "omim_gene": [
                    "601521"
                ],
                "alias_name": null,
                "gene_symbol": "ESM1",
                "hgnc_symbol": "ESM1",
                "hgnc_release": "2017-11-03",
                "ensembl_genes": {
                    "GRch37": {
                        "82": {
                            "location": "5:54273692-54318499",
                            "ensembl_id": "ENSG00000164283"
                        }
                    },
                    "GRch38": {
                        "90": {
                            "location": "5:54977864-55022671",
                            "ensembl_id": "ENSG00000164283"
                        }
                    }
                },
                "hgnc_date_symbol_changed": "2000-01-07"
            },
            "entity_type": "gene",
            "entity_name": "ESM1",
            "confidence_level": "3",
            "penetrance": null,
            "mode_of_pathogenicity": "",
            "publications": [],
            "evidence": [
                "Expert list",
                "Expert Review Green"
            ],
            "phenotypes": [],
            "mode_of_inheritance": "Unknown",
            "tags": [
                "umccr"
            ],
            "panel": {
                "id": 243,
                "hash_id": null,
                "name": "Immune_markers_WTS_UMCCR",
                "disease_group": "Cancer",
                "disease_sub_group": "",
                "description": "Author: Jacek Marzec, jacek.marzec@unimelb.edu.au\r\n\r\nPurpose: panel of immune markers used to assess pre-existing anti-cancer immunity and likelihood of response to immunotherapy. This set of genes is used in UMCCR WTS report \"Immune markers\" section\r\n\r\nSource: https://www.omniseq.com\r\n\r\nGithub: https://github.com/umccr/RNAsum",
                "status": "public",
                "version": "0.77",
                "version_created": "2025-11-03T15:30:48.145923+11:00",
                "relevant_disorders": [],
                "stats": {
                    "number_of_genes": 71,
                    "number_of_strs": 0,
                    "number_of_regions": 0
                },
                "types": [],
                "child_panel_ids": []
            },
            "transcript": null
        },
        {
            "gene_data": {
                "alias": [
                    "TBR2"
                ],
                "biotype": "protein_coding",
                "hgnc_id": "HGNC:3372",
                "gene_name": "eomesodermin",
                "omim_gene": [
                    "604615"
                ],
                "alias_name": [
                    "T-box brain2"
                ],
                "gene_symbol": "EOMES",
                "hgnc_symbol": "EOMES",
                "hgnc_release": "2017-11-03",
                "ensembl_genes": {
                    "GRch37": {
                        "82": {
                            "location": "3:27757440-27764206",
                            "ensembl_id": "ENSG00000163508"
                        }
                    },
                    "GRch38": {
                        "90": {
                            "location": "3:27715949-27722711",
                            "ensembl_id": "ENSG00000163508"
                        }
                    }
                },
                "hgnc_date_symbol_changed": "1998-09-15"
            },
            "entity_type": "gene",
            "entity_name": "EOMES",
            "confidence_level": "3",
            "penetrance": null,
            "mode_of_pathogenicity": "",
            "publications": [],
            "evidence": [
                "Expert list",
                "Expert Review Green"
            ],
            "phenotypes": [],
            "mode_of_inheritance": "Unknown",
            "tags": [
                "umccr"
            ],
            "panel": {
                "id": 243,
                "hash_id": null,
                "name": "Immune_markers_WTS_UMCCR",
                "disease_group": "Cancer",
                "disease_sub_group": "",
                "description": "Author: Jacek Marzec, jacek.marzec@unimelb.edu.au\r\n\r\nPurpose: panel of immune markers used to assess pre-existing anti-cancer immunity and likelihood of response to immunotherapy. This set of genes is used in UMCCR WTS report \"Immune markers\" section\r\n\r\nSource: https://www.omniseq.com\r\n\r\nGithub: https://github.com/umccr/RNAsum",
                "status": "public",
                "version": "0.77",
                "version_created": "2025-11-03T15:30:48.145923+11:00",
                "relevant_disorders": [],
                "stats": {
                    "number_of_genes": 71,
                    "number_of_strs": 0,
                    "number_of_regions": 0
                },
                "types": [],
                "child_panel_ids": []
            },
            "transcript": null
        },
        {
            "gene_data": {
                "alias": [
                    "NTPDase-1",
                    "ATPDase",
                    "SPG64"
                ],
                "biotype": "protein_coding",
                "hgnc_id": "HGNC:3363",
                "gene_name": "ectonucleoside triphosphate diphosphohydrolase 1",
                "omim_gene": [
                    "601752"
                ],
                "alias_name": null,
                "gene_symbol": "ENTPD1",
                "hgnc_symbol": "ENTPD1",
                "hgnc_release": "2017-11-03",
                "ensembl_genes": {
                    "GRch37": {
                        "82": {
                            "location": "10:97471536-97637023",
                            "ensembl_id": "ENSG00000138185"
                        }
                    },
                    "GRch38": {
                        "90": {
                            "location": "10:95711779-95869695",
                            "ensembl_id": "ENSG00000138185"
                        }
                    }
                },
                "hgnc_date_symbol_changed": "1994-12-09"
            },
            "entity_type": "gene",
            "entity_name": "ENTPD1",
            "confidence_level": "3",
            "penetrance": null,
            "mode_of_pathogenicity": "",
            "publications": [],
            "evidence": [
                "Expert list",
                "Expert Review Green"
            ],
            "phenotypes": [],
            "mode_of_inheritance": "Unknown",
            "tags": [
                "umccr"
            ],
            "panel": {
                "id": 243,
                "hash_id": null,
                "name": "Immune_markers_WTS_UMCCR",
                "disease_group": "Cancer",
                "disease_sub_group": "",
                "description": "Author: Jacek Marzec, jacek.marzec@unimelb.edu.au\r\n\r\nPurpose: panel of immune markers used to assess pre-existing anti-cancer immunity and likelihood of response to immunotherapy. This set of genes is used in UMCCR WTS report \"Immune markers\" section\r\n\r\nSource: https://www.omniseq.com\r\n\r\nGithub: https://github.com/umccr/RNAsum",
                "status": "public",
                "version": "0.77",
                "version_created": "2025-11-03T15:30:48.145923+11:00",
                "relevant_disorders": [],
                "stats": {
                    "number_of_genes": 71,
                    "number_of_strs": 0,
                    "number_of_regions": 0
                },
                "types": [],
                "child_panel_ids": []
            },
            "transcript": null
        },
        {
            "gene_data": {
                "alias": [
                    "RIG-I",
                    "FLJ13599",
                    "DKFZp434J1111"
                ],
                "biotype": "protein_coding",
                "hgnc_id": "HGNC:19102",
                "gene_name": "DExD/H-box helicase 58",
                "omim_gene": [
                    "609631"
                ],
                "alias_name": [
                    "RNA helicase RIG-I",
                    "retinoic acid inducible gene I"
                ],
                "gene_symbol": "DDX58",
                "hgnc_symbol": "DDX58",
                "hgnc_release": "2017-11-03",
                "ensembl_genes": {
                    "GRch37": {
                        "82": {
                            "location": "9:32455300-32526322",
                            "ensembl_id": "ENSG00000107201"
                        }
                    },
                    "GRch38": {
                        "90": {
                            "location": "9:32455705-32526324",
                            "ensembl_id": "ENSG00000107201"
                        }
                    }
                },
                "hgnc_date_symbol_changed": "2004-05-10"
            },
            "entity_type": "gene",
            "entity_name": "DDX58",
            "confidence_level": "3",
            "penetrance": null,
            "mode_of_pathogenicity": "",
            "publications": [],
            "evidence": [
                "Expert list",
                "Expert Review Green"
            ],
            "phenotypes": [],
            "mode_of_inheritance": "Unknown",
            "tags": [
                "umccr"
            ],
            "panel": {
                "id": 243,
                "hash_id": null,
                "name": "Immune_markers_WTS_UMCCR",
                "disease_group": "Cancer",
                "disease_sub_group": "",
                "description": "Author: Jacek Marzec, jacek.marzec@unimelb.edu.au\r\n\r\nPurpose: panel of immune markers used to assess pre-existing anti-cancer immunity and likelihood of response to immunotherapy. This set of genes is used in UMCCR WTS report \"Immune markers\" section\r\n\r\nSource: https://www.omniseq.com\r\n\r\nGithub: https://github.com/umccr/RNAsum",
                "status": "public",
                "version": "0.77",
                "version_created": "2025-11-03T15:30:48.145923+11:00",
                "relevant_disorders": [],
                "stats": {
                    "number_of_genes": 71,
                    "number_of_strs": 0,
                    "number_of_regions": 0
                },
                "types": [],
                "child_panel_ids": []
            },
            "transcript": null
        },
        {
            "gene_data": {
                "alias": [
                    "TYMSTR",
                    "STRL33",
                    "BONZO",
                    "CD186"
                ],
                "biotype": "protein_coding",
                "hgnc_id": "HGNC:16647",
                "gene_name": "C-X-C motif chemokine receptor 6",
                "omim_gene": [
                    "605163"
                ],
                "alias_name": null,
                "gene_symbol": "CXCR6",
                "hgnc_symbol": "CXCR6",
                "hgnc_release": "2017-11-03",
                "ensembl_genes": {
                    "GRch37": {
                        "82": {
                            "location": "3:45982425-45989845",
                            "ensembl_id": "ENSG00000172215"
                        }
                    },
                    "GRch38": {
                        "90": {
                            "location": "3:45940933-45948353",
                            "ensembl_id": "ENSG00000172215"
                        }
                    }
                },
                "hgnc_date_symbol_changed": "2002-08-23"
            },
            "entity_type": "gene",
            "entity_name": "CXCR6",
            "confidence_level": "3",
            "penetrance": null,
            "mode_of_pathogenicity": "",
            "publications": [],
            "evidence": [
                "Expert list",
                "Expert Review Green"
            ],
            "phenotypes": [],
            "mode_of_inheritance": "Unknown",
            "tags": [
                "umccr"
            ],
            "panel": {
                "id": 243,
                "hash_id": null,
                "name": "Immune_markers_WTS_UMCCR",
                "disease_group": "Cancer",
                "disease_sub_group": "",
                "description": "Author: Jacek Marzec, jacek.marzec@unimelb.edu.au\r\n\r\nPurpose: panel of immune markers used to assess pre-existing anti-cancer immunity and likelihood of response to immunotherapy. This set of genes is used in UMCCR WTS report \"Immune markers\" section\r\n\r\nSource: https://www.omniseq.com\r\n\r\nGithub: https://github.com/umccr/RNAsum",
                "status": "public",
                "version": "0.77",
                "version_created": "2025-11-03T15:30:48.145923+11:00",
                "relevant_disorders": [],
                "stats": {
                    "number_of_genes": 71,
                    "number_of_strs": 0,
                    "number_of_regions": 0
                },
                "types": [],
                "child_panel_ids": []
            },
            "transcript": null
        },
        {
            "gene_data": {
                "alias": [
                    "SCYB9",
                    "Humig",
                    "crg-10"
                ],
                "biotype": "protein_coding",
                "hgnc_id": "HGNC:7098",
                "gene_name": "C-X-C motif chemokine ligand 9",
                "omim_gene": [
                    "601704"
                ],
                "alias_name": null,
                "gene_symbol": "CXCL9",
                "hgnc_symbol": "CXCL9",
                "hgnc_release": "2017-11-03",
                "ensembl_genes": {
                    "GRch37": {
                        "82": {
                            "location": "4:76922428-76928641",
                            "ensembl_id": "ENSG00000138755"
                        }
                    },
                    "GRch38": {
                        "90": {
                            "location": "4:76001275-76007488",
                            "ensembl_id": "ENSG00000138755"
                        }
                    }
                },
                "hgnc_date_symbol_changed": "2002-08-23"
            },
            "entity_type": "gene",
            "entity_name": "CXCL9",
            "confidence_level": "3",
            "penetrance": null,
            "mode_of_pathogenicity": "",
            "publications": [],
            "evidence": [
                "Expert list",
                "Expert Review Green"
            ],
            "phenotypes": [],
            "mode_of_inheritance": "Unknown",
            "tags": [
                "umccr"
            ],
            "panel": {
                "id": 243,
                "hash_id": null,
                "name": "Immune_markers_WTS_UMCCR",
                "disease_group": "Cancer",
                "disease_sub_group": "",
                "description": "Author: Jacek Marzec, jacek.marzec@unimelb.edu.au\r\n\r\nPurpose: panel of immune markers used to assess pre-existing anti-cancer immunity and likelihood of response to immunotherapy. This set of genes is used in UMCCR WTS report \"Immune markers\" section\r\n\r\nSource: https://www.omniseq.com\r\n\r\nGithub: https://github.com/umccr/RNAsum",
                "status": "public",
                "version": "0.77",
                "version_created": "2025-11-03T15:30:48.145923+11:00",
                "relevant_disorders": [],
                "stats": {
                    "number_of_genes": 71,
                    "number_of_strs": 0,
                    "number_of_regions": 0
                },
                "types": [],
                "child_panel_ids": []
            },
            "transcript": null
        },
        {
            "gene_data": {
                "alias": [
                    "SCYB8",
                    "LUCT",
                    "LECT",
                    "MDNCF",
                    "TSG-1",
                    "IL-8",
                    "NAP-1",
                    "3-10C",
                    "MONAP",
                    "AMCF-I",
                    "LYNAP",
                    "NAF",
                    "b-ENAP",
                    "GCP-1",
                    "K60",
                    "GCP1",
                    "NAP1"
                ],
                "biotype": "protein_coding",
                "hgnc_id": "HGNC:6025",
                "gene_name": "C-X-C motif chemokine ligand 8",
                "omim_gene": [
                    "146930"
                ],
                "alias_name": [
                    "neutrophil-activating peptide 1",
                    "granulocyte chemotactic protein 1",
                    "monocyte-derived neutrophil chemotactic factor",
                    "lung giant cell carcinoma-derived chemotactic protein",
                    "tumor necrosis factor-induced gene 1",
                    "monocyte-derived neutrophil-activating peptide",
                    "lymphocyte derived neutrophil activating peptide",
                    "beta endothelial cell-derived neutrophil activating peptide",
                    "alveolar macrophage chemotactic factor I"
                ],
                "gene_symbol": "CXCL8",
                "hgnc_symbol": "CXCL8",
                "hgnc_release": "2017-11-03",
                "ensembl_genes": {
                    "GRch37": {
                        "82": {
                            "location": "4:74606223-74609433",
                            "ensembl_id": "ENSG00000169429"
                        }
                    },
                    "GRch38": {
                        "90": {
                            "location": "4:73740506-73743716",
                            "ensembl_id": "ENSG00000169429"
                        }
                    }
                },
                "hgnc_date_symbol_changed": "2014-04-10"
            },
            "entity_type": "gene",
            "entity_name": "CXCL8",
            "confidence_level": "3",
            "penetrance": null,
            "mode_of_pathogenicity": "",
            "publications": [],
            "evidence": [
                "Expert list",
                "Expert Review Green"
            ],
            "phenotypes": [],
            "mode_of_inheritance": "Unknown",
            "tags": [
                "umccr"
            ],
            "panel": {
                "id": 243,
                "hash_id": null,
                "name": "Immune_markers_WTS_UMCCR",
                "disease_group": "Cancer",
                "disease_sub_group": "",
                "description": "Author: Jacek Marzec, jacek.marzec@unimelb.edu.au\r\n\r\nPurpose: panel of immune markers used to assess pre-existing anti-cancer immunity and likelihood of response to immunotherapy. This set of genes is used in UMCCR WTS report \"Immune markers\" section\r\n\r\nSource: https://www.omniseq.com\r\n\r\nGithub: https://github.com/umccr/RNAsum",
                "status": "public",
                "version": "0.77",
                "version_created": "2025-11-03T15:30:48.145923+11:00",
                "relevant_disorders": [],
                "stats": {
                    "number_of_genes": 71,
                    "number_of_strs": 0,
                    "number_of_regions": 0
                },
                "types": [],
                "child_panel_ids": []
            },
            "transcript": null
        },
        {
            "gene_data": {
                "alias": [
                    "IFI10",
                    "IP-10",
                    "crg-2",
                    "mob-1",
                    "C7",
                    "gIP-10"
                ],
                "biotype": "protein_coding",
                "hgnc_id": "HGNC:10637",
                "gene_name": "C-X-C motif chemokine ligand 10",
                "omim_gene": [
                    "147310"
                ],
                "alias_name": null,
                "gene_symbol": "CXCL10",
                "hgnc_symbol": "CXCL10",
                "hgnc_release": "2017-11-03",
                "ensembl_genes": {
                    "GRch37": {
                        "82": {
                            "location": "4:76942273-76944650",
                            "ensembl_id": "ENSG00000169245"
                        }
                    },
                    "GRch38": {
                        "90": {
                            "location": "4:76021117-76023497",
                            "ensembl_id": "ENSG00000169245"
                        }
                    }
                },
                "hgnc_date_symbol_changed": "2002-08-23"
            },
            "entity_type": "gene",
            "entity_name": "CXCL10",
            "confidence_level": "3",
            "penetrance": null,
            "mode_of_pathogenicity": "",
            "publications": [],
            "evidence": [
                "Expert list",
                "Expert Review Green"
            ],
            "phenotypes": [],
            "mode_of_inheritance": "Unknown",
            "tags": [
                "umccr"
            ],
            "panel": {
                "id": 243,
                "hash_id": null,
                "name": "Immune_markers_WTS_UMCCR",
                "disease_group": "Cancer",
                "disease_sub_group": "",
                "description": "Author: Jacek Marzec, jacek.marzec@unimelb.edu.au\r\n\r\nPurpose: panel of immune markers used to assess pre-existing anti-cancer immunity and likelihood of response to immunotherapy. This set of genes is used in UMCCR WTS report \"Immune markers\" section\r\n\r\nSource: https://www.omniseq.com\r\n\r\nGithub: https://github.com/umccr/RNAsum",
                "status": "public",
                "version": "0.77",
                "version_created": "2025-11-03T15:30:48.145923+11:00",
                "relevant_disorders": [],
                "stats": {
                    "number_of_genes": 71,
                    "number_of_strs": 0,
                    "number_of_regions": 0
                },
                "types": [],
                "child_panel_ids": []
            },
            "transcript": null
        },
        {
            "gene_data": {
                "alias": [
                    "CD152",
                    "CD",
                    "GSE"
                ],
                "biotype": "protein_coding",
                "hgnc_id": "HGNC:2505",
                "gene_name": "cytotoxic T-lymphocyte associated protein 4",
                "omim_gene": [
                    "123890"
                ],
                "alias_name": null,
                "gene_symbol": "CTLA4",
                "hgnc_symbol": "CTLA4",
                "hgnc_release": "2017-11-03",
                "ensembl_genes": {
                    "GRch37": {
                        "82": {
                            "location": "2:204732509-204738683",
                            "ensembl_id": "ENSG00000163599"
                        }
                    },
                    "GRch38": {
                        "90": {
                            "location": "2:203867786-203873960",
                            "ensembl_id": "ENSG00000163599"
                        }
                    }
                },
                "hgnc_date_symbol_changed": "1989-05-25"
            },
            "entity_type": "gene",
            "entity_name": "CTLA4",
            "confidence_level": "3",
            "penetrance": null,
            "mode_of_pathogenicity": "",
            "publications": [],
            "evidence": [
                "Expert list",
                "Expert Review Green"
            ],
            "phenotypes": [],
            "mode_of_inheritance": "Unknown",
            "tags": [
                "umccr"
            ],
            "panel": {
                "id": 243,
                "hash_id": null,
                "name": "Immune_markers_WTS_UMCCR",
                "disease_group": "Cancer",
                "disease_sub_group": "",
                "description": "Author: Jacek Marzec, jacek.marzec@unimelb.edu.au\r\n\r\nPurpose: panel of immune markers used to assess pre-existing anti-cancer immunity and likelihood of response to immunotherapy. This set of genes is used in UMCCR WTS report \"Immune markers\" section\r\n\r\nSource: https://www.omniseq.com\r\n\r\nGithub: https://github.com/umccr/RNAsum",
                "status": "public",
                "version": "0.77",
                "version_created": "2025-11-03T15:30:48.145923+11:00",
                "relevant_disorders": [],
                "stats": {
                    "number_of_genes": 71,
                    "number_of_strs": 0,
                    "number_of_regions": 0
                },
                "types": [],
                "child_panel_ids": []
            },
            "transcript": null
        },
        {
            "gene_data": {
                "alias": [
                    "IGFBP8",
                    "CCN2"
                ],
                "biotype": "protein_coding",
                "hgnc_id": "HGNC:2500",
                "gene_name": "connective tissue growth factor",
                "omim_gene": [
                    "121009"
                ],
                "alias_name": null,
                "gene_symbol": "CTGF",
                "hgnc_symbol": "CTGF",
                "hgnc_release": "2017-11-03",
                "ensembl_genes": {
                    "GRch37": {
                        "82": {
                            "location": "6:132269316-132272513",
                            "ensembl_id": "ENSG00000118523"
                        }
                    },
                    "GRch38": {
                        "90": {
                            "location": "6:131948176-131951373",
                            "ensembl_id": "ENSG00000118523"
                        }
                    }
                },
                "hgnc_date_symbol_changed": "1992-12-01"
            },
            "entity_type": "gene",
            "entity_name": "CTGF",
            "confidence_level": "3",
            "penetrance": null,
            "mode_of_pathogenicity": "",
            "publications": [],
            "evidence": [
                "Expert list",
                "Expert Review Green"
            ],
            "phenotypes": [],
            "mode_of_inheritance": "Unknown",
            "tags": [
                "umccr"
            ],
            "panel": {
                "id": 243,
                "hash_id": null,
                "name": "Immune_markers_WTS_UMCCR",
                "disease_group": "Cancer",
                "disease_sub_group": "",
                "description": "Author: Jacek Marzec, jacek.marzec@unimelb.edu.au\r\n\r\nPurpose: panel of immune markers used to assess pre-existing anti-cancer immunity and likelihood of response to immunotherapy. This set of genes is used in UMCCR WTS report \"Immune markers\" section\r\n\r\nSource: https://www.omniseq.com\r\n\r\nGithub: https://github.com/umccr/RNAsum",
                "status": "public",
                "version": "0.77",
                "version_created": "2025-11-03T15:30:48.145923+11:00",
                "relevant_disorders": [],
                "stats": {
                    "number_of_genes": 71,
                    "number_of_strs": 0,
                    "number_of_regions": 0
                },
                "types": [],
                "child_panel_ids": []
            },
            "transcript": null
        },
        {
            "gene_data": {
                "alias": [
                    "C-FMS",
                    "CSFR",
                    "CD115"
                ],
                "biotype": "protein_coding",
                "hgnc_id": "HGNC:2433",
                "gene_name": "colony stimulating factor 1 receptor",
                "omim_gene": [
                    "164770"
                ],
                "alias_name": null,
                "gene_symbol": "CSF1R",
                "hgnc_symbol": "CSF1R",
                "hgnc_release": "2017-11-03",
                "ensembl_genes": {
                    "GRch37": {
                        "82": {
                            "location": "5:149432854-149492935",
                            "ensembl_id": "ENSG00000182578"
                        }
                    },
                    "GRch38": {
                        "90": {
                            "location": "5:150053291-150113372",
                            "ensembl_id": "ENSG00000182578"
                        }
                    }
                },
                "hgnc_date_symbol_changed": "2001-06-22"
            },
            "entity_type": "gene",
            "entity_name": "CSF1R",
            "confidence_level": "3",
            "penetrance": null,
            "mode_of_pathogenicity": "",
            "publications": [],
            "evidence": [
                "Expert list",
                "Expert Review Green"
            ],
            "phenotypes": [],
            "mode_of_inheritance": "Unknown",
            "tags": [
                "umccr"
            ],
            "panel": {
                "id": 243,
                "hash_id": null,
                "name": "Immune_markers_WTS_UMCCR",
                "disease_group": "Cancer",
                "disease_sub_group": "",
                "description": "Author: Jacek Marzec, jacek.marzec@unimelb.edu.au\r\n\r\nPurpose: panel of immune markers used to assess pre-existing anti-cancer immunity and likelihood of response to immunotherapy. This set of genes is used in UMCCR WTS report \"Immune markers\" section\r\n\r\nSource: https://www.omniseq.com\r\n\r\nGithub: https://github.com/umccr/RNAsum",
                "status": "public",
                "version": "0.77",
                "version_created": "2025-11-03T15:30:48.145923+11:00",
                "relevant_disorders": [],
                "stats": {
                    "number_of_genes": 71,
                    "number_of_strs": 0,
                    "number_of_regions": 0
                },
                "types": [],
                "child_panel_ids": []
            },
            "transcript": null
        },
        {
            "gene_data": {
                "alias": [
                    "OI4"
                ],
                "biotype": "protein_coding",
                "hgnc_id": "HGNC:2197",
                "gene_name": "collagen type I alpha 1 chain",
                "omim_gene": [
                    "120150"
                ],
                "alias_name": null,
                "gene_symbol": "COL1A1",
                "hgnc_symbol": "COL1A1",
                "hgnc_release": "2017-11-03",
                "ensembl_genes": {
                    "GRch37": {
                        "82": {
                            "location": "17:48260650-48278993",
                            "ensembl_id": "ENSG00000108821"
                        }
                    },
                    "GRch38": {
                        "90": {
                            "location": "17:50183289-50201632",
                            "ensembl_id": "ENSG00000108821"
                        }
                    }
                },
                "hgnc_date_symbol_changed": "2001-06-22"
            },
            "entity_type": "gene",
            "entity_name": "COL1A1",
            "confidence_level": "3",
            "penetrance": null,
            "mode_of_pathogenicity": "",
            "publications": [],
            "evidence": [
                "Expert list",
                "Expert Review Green"
            ],
            "phenotypes": [],
            "mode_of_inheritance": "Unknown",
            "tags": [
                "umccr"
            ],
            "panel": {
                "id": 243,
                "hash_id": null,
                "name": "Immune_markers_WTS_UMCCR",
                "disease_group": "Cancer",
                "disease_sub_group": "",
                "description": "Author: Jacek Marzec, jacek.marzec@unimelb.edu.au\r\n\r\nPurpose: panel of immune markers used to assess pre-existing anti-cancer immunity and likelihood of response to immunotherapy. This set of genes is used in UMCCR WTS report \"Immune markers\" section\r\n\r\nSource: https://www.omniseq.com\r\n\r\nGithub: https://github.com/umccr/RNAsum",
                "status": "public",
                "version": "0.77",
                "version_created": "2025-11-03T15:30:48.145923+11:00",
                "relevant_disorders": [],
                "stats": {
                    "number_of_genes": 71,
                    "number_of_strs": 0,
                    "number_of_regions": 0
                },
                "types": [],
                "child_panel_ids": []
            },
            "transcript": null
        },
        {
            "gene_data": {
                "alias": [],
                "biotype": "protein_coding",
                "hgnc_id": "HGNC:1707",
                "gene_name": "CD8b molecule",
                "omim_gene": [
                    "186730"
                ],
                "alias_name": null,
                "gene_symbol": "CD8B",
                "hgnc_symbol": "CD8B",
                "hgnc_release": "2017-11-03",
                "ensembl_genes": {
                    "GRch37": {
                        "82": {
                            "location": "2:87042462-87089047",
                            "ensembl_id": "ENSG00000172116"
                        }
                    },
                    "GRch38": {
                        "90": {
                            "location": "2:86815339-86861924",
                            "ensembl_id": "ENSG00000172116"
                        }
                    }
                },
                "hgnc_date_symbol_changed": "2006-03-09"
            },
            "entity_type": "gene",
            "entity_name": "CD8B",
            "confidence_level": "3",
            "penetrance": null,
            "mode_of_pathogenicity": "",
            "publications": [],
            "evidence": [
                "Expert list",
                "Expert Review Green"
            ],
            "phenotypes": [],
            "mode_of_inheritance": "Unknown",
            "tags": [
                "umccr"
            ],
            "panel": {
                "id": 243,
                "hash_id": null,
                "name": "Immune_markers_WTS_UMCCR",
                "disease_group": "Cancer",
                "disease_sub_group": "",
                "description": "Author: Jacek Marzec, jacek.marzec@unimelb.edu.au\r\n\r\nPurpose: panel of immune markers used to assess pre-existing anti-cancer immunity and likelihood of response to immunotherapy. This set of genes is used in UMCCR WTS report \"Immune markers\" section\r\n\r\nSource: https://www.omniseq.com\r\n\r\nGithub: https://github.com/umccr/RNAsum",
                "status": "public",
                "version": "0.77",
                "version_created": "2025-11-03T15:30:48.145923+11:00",
                "relevant_disorders": [],
                "stats": {
                    "number_of_genes": 71,
                    "number_of_strs": 0,
                    "number_of_regions": 0
                },
                "types": [],
                "child_panel_ids": []
            },
            "transcript": null
        },
        {
            "gene_data": {
                "alias": [],
                "biotype": "protein_coding",
                "hgnc_id": "HGNC:1706",
                "gene_name": "CD8a molecule",
                "omim_gene": [
                    "186910"
                ],
                "alias_name": null,
                "gene_symbol": "CD8A",
                "hgnc_symbol": "CD8A",
                "hgnc_release": "2017-11-03",
                "ensembl_genes": {
                    "GRch37": {
                        "82": {
                            "location": "2:87011729-87035519",
                            "ensembl_id": "ENSG00000153563"
                        }
                    },
                    "GRch38": {
                        "90": {
                            "location": "2:86784610-86808396",
                            "ensembl_id": "ENSG00000153563"
                        }
                    }
                },
                "hgnc_date_symbol_changed": "1986-01-01"
            },
            "entity_type": "gene",
            "entity_name": "CD8A",
            "confidence_level": "3",
            "penetrance": null,
            "mode_of_pathogenicity": "",
            "publications": [],
            "evidence": [
                "Expert list",
                "Expert Review Green"
            ],
            "phenotypes": [],
            "mode_of_inheritance": "Unknown",
            "tags": [
                "umccr"
            ],
            "panel": {
                "id": 243,
                "hash_id": null,
                "name": "Immune_markers_WTS_UMCCR",
                "disease_group": "Cancer",
                "disease_sub_group": "",
                "description": "Author: Jacek Marzec, jacek.marzec@unimelb.edu.au\r\n\r\nPurpose: panel of immune markers used to assess pre-existing anti-cancer immunity and likelihood of response to immunotherapy. This set of genes is used in UMCCR WTS report \"Immune markers\" section\r\n\r\nSource: https://www.omniseq.com\r\n\r\nGithub: https://github.com/umccr/RNAsum",
                "status": "public",
                "version": "0.77",
                "version_created": "2025-11-03T15:30:48.145923+11:00",
                "relevant_disorders": [],
                "stats": {
                    "number_of_genes": 71,
                    "number_of_strs": 0,
                    "number_of_regions": 0
                },
                "types": [],
                "child_panel_ids": []
            },
            "transcript": null
        },
        {
            "gene_data": {
                "alias": [
                    "B7.2",
                    "B7-2"
                ],
                "biotype": "protein_coding",
                "hgnc_id": "HGNC:1705",
                "gene_name": "CD86 molecule",
                "omim_gene": [
                    "601020"
                ],
                "alias_name": [
                    "B-lymphocyte antigen B7-2"
                ],
                "gene_symbol": "CD86",
                "hgnc_symbol": "CD86",
                "hgnc_release": "2017-11-03",
                "ensembl_genes": {
                    "GRch37": {
                        "82": {
                            "location": "3:121774213-121839983",
                            "ensembl_id": "ENSG00000114013"
                        }
                    },
                    "GRch38": {
                        "90": {
                            "location": "3:122055366-122121139",
                            "ensembl_id": "ENSG00000114013"
                        }
                    }
                },
                "hgnc_date_symbol_changed": "1994-12-07"
            },
            "entity_type": "gene",
            "entity_name": "CD86",
            "confidence_level": "3",
            "penetrance": null,
            "mode_of_pathogenicity": "",
            "publications": [],
            "evidence": [
                "Expert list",
                "Expert Review Green"
            ],
            "phenotypes": [],
            "mode_of_inheritance": "Unknown",
            "tags": [
                "umccr"
            ],
            "panel": {
                "id": 243,
                "hash_id": null,
                "name": "Immune_markers_WTS_UMCCR",
                "disease_group": "Cancer",
                "disease_sub_group": "",
                "description": "Author: Jacek Marzec, jacek.marzec@unimelb.edu.au\r\n\r\nPurpose: panel of immune markers used to assess pre-existing anti-cancer immunity and likelihood of response to immunotherapy. This set of genes is used in UMCCR WTS report \"Immune markers\" section\r\n\r\nSource: https://www.omniseq.com\r\n\r\nGithub: https://github.com/umccr/RNAsum",
                "status": "public",
                "version": "0.77",
                "version_created": "2025-11-03T15:30:48.145923+11:00",
                "relevant_disorders": [],
                "stats": {
                    "number_of_genes": 71,
                    "number_of_strs": 0,
                    "number_of_regions": 0
                },
                "types": [],
                "child_panel_ids": []
            },
            "transcript": null
        },
        {
            "gene_data": {
                "alias": [
                    "B7.1",
                    "B7-1"
                ],
                "biotype": "protein_coding",
                "hgnc_id": "HGNC:1700",
                "gene_name": "CD80 molecule",
                "omim_gene": [
                    "112203"
                ],
                "alias_name": [
                    "B-lymphocyte activation antigen B7"
                ],
                "gene_symbol": "CD80",
                "hgnc_symbol": "CD80",
                "hgnc_release": "2017-11-03",
                "ensembl_genes": {
                    "GRch37": {
                        "82": {
                            "location": "3:119243140-119278449",
                            "ensembl_id": "ENSG00000121594"
                        }
                    },
                    "GRch38": {
                        "90": {
                            "location": "3:119524293-119559602",
                            "ensembl_id": "ENSG00000121594"
                        }
                    }
                },
                "hgnc_date_symbol_changed": "1993-12-14"
            },
            "entity_type": "gene",
            "entity_name": "CD80",
            "confidence_level": "3",
            "penetrance": null,
            "mode_of_pathogenicity": "",
            "publications": [],
            "evidence": [
                "Expert list",
                "Expert Review Green"
            ],
            "phenotypes": [],
            "mode_of_inheritance": "Unknown",
            "tags": [
                "umccr"
            ],
            "panel": {
                "id": 243,
                "hash_id": null,
                "name": "Immune_markers_WTS_UMCCR",
                "disease_group": "Cancer",
                "disease_sub_group": "",
                "description": "Author: Jacek Marzec, jacek.marzec@unimelb.edu.au\r\n\r\nPurpose: panel of immune markers used to assess pre-existing anti-cancer immunity and likelihood of response to immunotherapy. This set of genes is used in UMCCR WTS report \"Immune markers\" section\r\n\r\nSource: https://www.omniseq.com\r\n\r\nGithub: https://github.com/umccr/RNAsum",
                "status": "public",
                "version": "0.77",
                "version_created": "2025-11-03T15:30:48.145923+11:00",
                "relevant_disorders": [],
                "stats": {
                    "number_of_genes": 71,
                    "number_of_strs": 0,
                    "number_of_regions": 0
                },
                "types": [],
                "child_panel_ids": []
            },
            "transcript": null
        },
        {
            "gene_data": {
                "alias": [
                    "B29"
                ],
                "biotype": "protein_coding",
                "hgnc_id": "HGNC:1699",
                "gene_name": "CD79b molecule",
                "omim_gene": [
                    "147245"
                ],
                "alias_name": null,
                "gene_symbol": "CD79B",
                "hgnc_symbol": "CD79B",
                "hgnc_release": "2017-11-03",
                "ensembl_genes": {
                    "GRch37": {
                        "82": {
                            "location": "17:62006100-62009714",
                            "ensembl_id": "ENSG00000007312"
                        }
                    },
                    "GRch38": {
                        "90": {
                            "location": "17:63928740-63932354",
                            "ensembl_id": "ENSG00000007312"
                        }
                    }
                },
                "hgnc_date_symbol_changed": "1992-08-04"
            },
            "entity_type": "gene",
            "entity_name": "CD79B",
            "confidence_level": "3",
            "penetrance": null,
            "mode_of_pathogenicity": "",
            "publications": [],
            "evidence": [
                "Expert list",
                "Expert Review Green"
            ],
            "phenotypes": [],
            "mode_of_inheritance": "Unknown",
            "tags": [
                "umccr"
            ],
            "panel": {
                "id": 243,
                "hash_id": null,
                "name": "Immune_markers_WTS_UMCCR",
                "disease_group": "Cancer",
                "disease_sub_group": "",
                "description": "Author: Jacek Marzec, jacek.marzec@unimelb.edu.au\r\n\r\nPurpose: panel of immune markers used to assess pre-existing anti-cancer immunity and likelihood of response to immunotherapy. This set of genes is used in UMCCR WTS report \"Immune markers\" section\r\n\r\nSource: https://www.omniseq.com\r\n\r\nGithub: https://github.com/umccr/RNAsum",
                "status": "public",
                "version": "0.77",
                "version_created": "2025-11-03T15:30:48.145923+11:00",
                "relevant_disorders": [],
                "stats": {
                    "number_of_genes": 71,
                    "number_of_strs": 0,
                    "number_of_regions": 0
                },
                "types": [],
                "child_panel_ids": []
            },
            "transcript": null
        },
        {
            "gene_data": {
                "alias": [
                    "CD40L",
                    "TRAP",
                    "gp39",
                    "hCD40L",
                    "CD154"
                ],
                "biotype": "protein_coding",
                "hgnc_id": "HGNC:11935",
                "gene_name": "CD40 ligand",
                "omim_gene": [
                    "300386"
                ],
                "alias_name": [
                    "CD40 antigen ligand",
                    "tumor necrosis factor (ligand) superfamily member 5",
                    "T-B cell-activating molecule",
                    "TNF-related activation protein",
                    "hyper-IgM syndrome"
                ],
                "gene_symbol": "CD40LG",
                "hgnc_symbol": "CD40LG",
                "hgnc_release": "2017-11-03",
                "ensembl_genes": {
                    "GRch37": {
                        "82": {
                            "location": "X:135730352-135742549",
                            "ensembl_id": "ENSG00000102245"
                        }
                    },
                    "GRch38": {
                        "90": {
                            "location": "X:136648193-136660390",
                            "ensembl_id": "ENSG00000102245"
                        }
                    }
                },
                "hgnc_date_symbol_changed": "2005-01-14"
            },
            "entity_type": "gene",
            "entity_name": "CD40LG",
            "confidence_level": "3",
            "penetrance": null,
            "mode_of_pathogenicity": "",
            "publications": [],
            "evidence": [
                "Expert list",
                "Expert Review Green"
            ],
            "phenotypes": [],
            "mode_of_inheritance": "Unknown",
            "tags": [
                "umccr"
            ],
            "panel": {
                "id": 243,
                "hash_id": null,
                "name": "Immune_markers_WTS_UMCCR",
                "disease_group": "Cancer",
                "disease_sub_group": "",
                "description": "Author: Jacek Marzec, jacek.marzec@unimelb.edu.au\r\n\r\nPurpose: panel of immune markers used to assess pre-existing anti-cancer immunity and likelihood of response to immunotherapy. This set of genes is used in UMCCR WTS report \"Immune markers\" section\r\n\r\nSource: https://www.omniseq.com\r\n\r\nGithub: https://github.com/umccr/RNAsum",
                "status": "public",
                "version": "0.77",
                "version_created": "2025-11-03T15:30:48.145923+11:00",
                "relevant_disorders": [],
                "stats": {
                    "number_of_genes": 71,
                    "number_of_strs": 0,
                    "number_of_regions": 0
                },
                "types": [],
                "child_panel_ids": []
            },
            "transcript": null
        },
        {
            "gene_data": {
                "alias": [
                    "p50",
                    "Bp50"
                ],
                "biotype": "protein_coding",
                "hgnc_id": "HGNC:11919",
                "gene_name": "CD40 molecule",
                "omim_gene": [
                    "109535"
                ],
                "alias_name": null,
                "gene_symbol": "CD40",
                "hgnc_symbol": "CD40",
                "hgnc_release": "2017-11-03",
                "ensembl_genes": {
                    "GRch37": {
                        "82": {
                            "location": "20:44746911-44758502",
                            "ensembl_id": "ENSG00000101017"
                        }
                    },
                    "GRch38": {
                        "90": {
                            "location": "20:46118272-46129863",
                            "ensembl_id": "ENSG00000101017"
                        }
                    }
                },
                "hgnc_date_symbol_changed": "2005-01-14"
            },
            "entity_type": "gene",
            "entity_name": "CD40",
            "confidence_level": "3",
            "penetrance": null,
            "mode_of_pathogenicity": "",
            "publications": [],
            "evidence": [
                "Expert list",
                "Expert Review Green"
            ],
            "phenotypes": [],
            "mode_of_inheritance": "Unknown",
            "tags": [
                "umccr"
            ],
            "panel": {
                "id": 243,
                "hash_id": null,
                "name": "Immune_markers_WTS_UMCCR",
                "disease_group": "Cancer",
                "disease_sub_group": "",
                "description": "Author: Jacek Marzec, jacek.marzec@unimelb.edu.au\r\n\r\nPurpose: panel of immune markers used to assess pre-existing anti-cancer immunity and likelihood of response to immunotherapy. This set of genes is used in UMCCR WTS report \"Immune markers\" section\r\n\r\nSource: https://www.omniseq.com\r\n\r\nGithub: https://github.com/umccr/RNAsum",
                "status": "public",
                "version": "0.77",
                "version_created": "2025-11-03T15:30:48.145923+11:00",
                "relevant_disorders": [],
                "stats": {
                    "number_of_genes": 71,
                    "number_of_strs": 0,
                    "number_of_regions": 0
                },
                "types": [],
                "child_panel_ids": []
            },
            "transcript": null
        },
        {
            "gene_data": {
                "alias": [],
                "biotype": "protein_coding",
                "hgnc_id": "HGNC:1678",
                "gene_name": "CD4 molecule",
                "omim_gene": [
                    "186940"
                ],
                "alias_name": null,
                "gene_symbol": "CD4",
                "hgnc_symbol": "CD4",
                "hgnc_release": "2017-11-03",
                "ensembl_genes": {
                    "GRch37": {
                        "82": {
                            "location": "12:6896024-6929974",
                            "ensembl_id": "ENSG00000010610"
                        }
                    },
                    "GRch38": {
                        "90": {
                            "location": "12:6786858-6820808",
                            "ensembl_id": "ENSG00000010610"
                        }
                    }
                },
                "hgnc_date_symbol_changed": "1986-01-01"
            },
            "entity_type": "gene",
            "entity_name": "CD4",
            "confidence_level": "3",
            "penetrance": null,
            "mode_of_pathogenicity": "",
            "publications": [],
            "evidence": [
                "Expert list",
                "Expert Review Green"
            ],
            "phenotypes": [],
            "mode_of_inheritance": "Unknown",
            "tags": [
                "umccr"
            ],
            "panel": {
                "id": 243,
                "hash_id": null,
                "name": "Immune_markers_WTS_UMCCR",
                "disease_group": "Cancer",
                "disease_sub_group": "",
                "description": "Author: Jacek Marzec, jacek.marzec@unimelb.edu.au\r\n\r\nPurpose: panel of immune markers used to assess pre-existing anti-cancer immunity and likelihood of response to immunotherapy. This set of genes is used in UMCCR WTS report \"Immune markers\" section\r\n\r\nSource: https://www.omniseq.com\r\n\r\nGithub: https://github.com/umccr/RNAsum",
                "status": "public",
                "version": "0.77",
                "version_created": "2025-11-03T15:30:48.145923+11:00",
                "relevant_disorders": [],
                "stats": {
                    "number_of_genes": 71,
                    "number_of_strs": 0,
                    "number_of_regions": 0
                },
                "types": [],
                "child_panel_ids": []
            },
            "transcript": null
        },
        {
            "gene_data": {
                "alias": [],
                "biotype": "protein_coding",
                "hgnc_id": "HGNC:1675",
                "gene_name": "CD3g molecule",
                "omim_gene": [
                    "186740"
                ],
                "alias_name": null,
                "gene_symbol": "CD3G",
                "hgnc_symbol": "CD3G",
                "hgnc_release": "2017-11-03",
                "ensembl_genes": {
                    "GRch37": {
                        "82": {
                            "location": "11:118215059-118225876",
                            "ensembl_id": "ENSG00000160654"
                        }
                    },
                    "GRch38": {
                        "90": {
                            "location": "11:118344344-118355161",
                            "ensembl_id": "ENSG00000160654"
                        }
                    }
                },
                "hgnc_date_symbol_changed": "1988-05-11"
            },
            "entity_type": "gene",
            "entity_name": "CD3G",
            "confidence_level": "3",
            "penetrance": null,
            "mode_of_pathogenicity": "",
            "publications": [],
            "evidence": [
                "Expert list",
                "Expert Review Green"
            ],
            "phenotypes": [],
            "mode_of_inheritance": "Unknown",
            "tags": [
                "umccr"
            ],
            "panel": {
                "id": 243,
                "hash_id": null,
                "name": "Immune_markers_WTS_UMCCR",
                "disease_group": "Cancer",
                "disease_sub_group": "",
                "description": "Author: Jacek Marzec, jacek.marzec@unimelb.edu.au\r\n\r\nPurpose: panel of immune markers used to assess pre-existing anti-cancer immunity and likelihood of response to immunotherapy. This set of genes is used in UMCCR WTS report \"Immune markers\" section\r\n\r\nSource: https://www.omniseq.com\r\n\r\nGithub: https://github.com/umccr/RNAsum",
                "status": "public",
                "version": "0.77",
                "version_created": "2025-11-03T15:30:48.145923+11:00",
                "relevant_disorders": [],
                "stats": {
                    "number_of_genes": 71,
                    "number_of_strs": 0,
                    "number_of_regions": 0
                },
                "types": [],
                "child_panel_ids": []
            },
            "transcript": null
        },
        {
            "gene_data": {
                "alias": [],
                "biotype": "protein_coding",
                "hgnc_id": "HGNC:1674",
                "gene_name": "CD3e molecule",
                "omim_gene": [
                    "186830"
                ],
                "alias_name": null,
                "gene_symbol": "CD3E",
                "hgnc_symbol": "CD3E",
                "hgnc_release": "2017-11-03",
                "ensembl_genes": {
                    "GRch37": {
                        "82": {
                            "location": "11:118175260-118186890",
                            "ensembl_id": "ENSG00000198851"
                        }
                    },
                    "GRch38": {
                        "90": {
                            "location": "11:118304545-118316175",
                            "ensembl_id": "ENSG00000198851"
                        }
                    }
                },
                "hgnc_date_symbol_changed": "1986-01-01"
            },
            "entity_type": "gene",
            "entity_name": "CD3E",
            "confidence_level": "3",
            "penetrance": null,
            "mode_of_pathogenicity": "",
            "publications": [],
            "evidence": [
                "Expert list",
                "Expert Review Green"
            ],
            "phenotypes": [],
            "mode_of_inheritance": "Unknown",
            "tags": [
                "umccr"
            ],
            "panel": {
                "id": 243,
                "hash_id": null,
                "name": "Immune_markers_WTS_UMCCR",
                "disease_group": "Cancer",
                "disease_sub_group": "",
                "description": "Author: Jacek Marzec, jacek.marzec@unimelb.edu.au\r\n\r\nPurpose: panel of immune markers used to assess pre-existing anti-cancer immunity and likelihood of response to immunotherapy. This set of genes is used in UMCCR WTS report \"Immune markers\" section\r\n\r\nSource: https://www.omniseq.com\r\n\r\nGithub: https://github.com/umccr/RNAsum",
                "status": "public",
                "version": "0.77",
                "version_created": "2025-11-03T15:30:48.145923+11:00",
                "relevant_disorders": [],
                "stats": {
                    "number_of_genes": 71,
                    "number_of_strs": 0,
                    "number_of_regions": 0
                },
                "types": [],
                "child_panel_ids": []
            },
            "transcript": null
        },
        {
            "gene_data": {
                "alias": [],
                "biotype": "protein_coding",
                "hgnc_id": "HGNC:1673",
                "gene_name": "CD3d molecule",
                "omim_gene": [
                    "186790"
                ],
                "alias_name": null,
                "gene_symbol": "CD3D",
                "hgnc_symbol": "CD3D",
                "hgnc_release": "2017-11-03",
                "ensembl_genes": {
                    "GRch37": {
                        "82": {
                            "location": "11:118209669-118213459",
                            "ensembl_id": "ENSG00000167286"
                        }
                    },
                    "GRch38": {
                        "90": {
                            "location": "11:118338954-118342744",
                            "ensembl_id": "ENSG00000167286"
                        }
                    }
                },
                "hgnc_date_symbol_changed": "1986-01-01"
            },
            "entity_type": "gene",
            "entity_name": "CD3D",
            "confidence_level": "3",
            "penetrance": null,
            "mode_of_pathogenicity": "",
            "publications": [],
            "evidence": [
                "Expert list",
                "Expert Review Green"
            ],
            "phenotypes": [],
            "mode_of_inheritance": "Unknown",
            "tags": [
                "umccr"
            ],
            "panel": {
                "id": 243,
                "hash_id": null,
                "name": "Immune_markers_WTS_UMCCR",
                "disease_group": "Cancer",
                "disease_sub_group": "",
                "description": "Author: Jacek Marzec, jacek.marzec@unimelb.edu.au\r\n\r\nPurpose: panel of immune markers used to assess pre-existing anti-cancer immunity and likelihood of response to immunotherapy. This set of genes is used in UMCCR WTS report \"Immune markers\" section\r\n\r\nSource: https://www.omniseq.com\r\n\r\nGithub: https://github.com/umccr/RNAsum",
                "status": "public",
                "version": "0.77",
                "version_created": "2025-11-03T15:30:48.145923+11:00",
                "relevant_disorders": [],
                "stats": {
                    "number_of_genes": 71,
                    "number_of_strs": 0,
                    "number_of_regions": 0
                },
                "types": [],
                "child_panel_ids": []
            },
            "transcript": null
        },
        {
            "gene_data": {
                "alias": [],
                "biotype": "protein_coding",
                "hgnc_id": "HGNC:1667",
                "gene_name": "CD38 molecule",
                "omim_gene": [
                    "107270"
                ],
                "alias_name": [
                    "ADP-ribosyl cyclase 1",
                    "NAD(+) nucleosidase"
                ],
                "gene_symbol": "CD38",
                "hgnc_symbol": "CD38",
                "hgnc_release": "2017-11-03",
                "ensembl_genes": {
                    "GRch37": {
                        "82": {
                            "location": "4:15779898-15854853",
                            "ensembl_id": "ENSG00000004468"
                        }
                    },
                    "GRch38": {
                        "90": {
                            "location": "4:15778275-15853230",
                            "ensembl_id": "ENSG00000004468"
                        }
                    }
                },
                "hgnc_date_symbol_changed": "1986-01-01"
            },
            "entity_type": "gene",
            "entity_name": "CD38",
            "confidence_level": "3",
            "penetrance": null,
            "mode_of_pathogenicity": "",
            "publications": [],
            "evidence": [
                "Expert list",
                "Expert Review Green"
            ],
            "phenotypes": [],
            "mode_of_inheritance": "Unknown",
            "tags": [
                "umccr"
            ],
            "panel": {
                "id": 243,
                "hash_id": null,
                "name": "Immune_markers_WTS_UMCCR",
                "disease_group": "Cancer",
                "disease_sub_group": "",
                "description": "Author: Jacek Marzec, jacek.marzec@unimelb.edu.au\r\n\r\nPurpose: panel of immune markers used to assess pre-existing anti-cancer immunity and likelihood of response to immunotherapy. This set of genes is used in UMCCR WTS report \"Immune markers\" section\r\n\r\nSource: https://www.omniseq.com\r\n\r\nGithub: https://github.com/umccr/RNAsum",
                "status": "public",
                "version": "0.77",
                "version_created": "2025-11-03T15:30:48.145923+11:00",
                "relevant_disorders": [],
                "stats": {
                    "number_of_genes": 71,
                    "number_of_strs": 0,
                    "number_of_regions": 0
                },
                "types": [],
                "child_panel_ids": []
            },
            "transcript": null
        },
        {
            "gene_data": {
                "alias": [],
                "biotype": "protein_coding",
                "hgnc_id": "HGNC:1653",
                "gene_name": "CD28 molecule",
                "omim_gene": [
                    "186760"
                ],
                "alias_name": [
                    "T-cell-specific surface glycoprotein"
                ],
                "gene_symbol": "CD28",
                "hgnc_symbol": "CD28",
                "hgnc_release": "2017-11-03",
                "ensembl_genes": {
                    "GRch37": {
                        "82": {
                            "location": "2:204571198-204603635",
                            "ensembl_id": "ENSG00000178562"
                        }
                    },
                    "GRch38": {
                        "90": {
                            "location": "2:203706475-203738912",
                            "ensembl_id": "ENSG00000178562"
                        }
                    }
                },
                "hgnc_date_symbol_changed": "1988-05-11"
            },
            "entity_type": "gene",
            "entity_name": "CD28",
            "confidence_level": "3",
            "penetrance": null,
            "mode_of_pathogenicity": "",
            "publications": [],
            "evidence": [
                "Expert list",
                "Expert Review Green"
            ],
            "phenotypes": [],
            "mode_of_inheritance": "Unknown",
            "tags": [
                "umccr"
            ],
            "panel": {
                "id": 243,
                "hash_id": null,
                "name": "Immune_markers_WTS_UMCCR",
                "disease_group": "Cancer",
                "disease_sub_group": "",
                "description": "Author: Jacek Marzec, jacek.marzec@unimelb.edu.au\r\n\r\nPurpose: panel of immune markers used to assess pre-existing anti-cancer immunity and likelihood of response to immunotherapy. This set of genes is used in UMCCR WTS report \"Immune markers\" section\r\n\r\nSource: https://www.omniseq.com\r\n\r\nGithub: https://github.com/umccr/RNAsum",
                "status": "public",
                "version": "0.77",
                "version_created": "2025-11-03T15:30:48.145923+11:00",
                "relevant_disorders": [],
                "stats": {
                    "number_of_genes": 71,
                    "number_of_strs": 0,
                    "number_of_regions": 0
                },
                "types": [],
                "child_panel_ids": []
            },
            "transcript": null
        },
        {
            "gene_data": {
                "alias": [
                    "B7-H",
                    "B7H1",
                    "PD-L1",
                    "PDL1",
                    "B7-H1"
                ],
                "biotype": "protein_coding",
                "hgnc_id": "HGNC:17635",
                "gene_name": "CD274 molecule",
                "omim_gene": [
                    "605402"
                ],
                "alias_name": [
                    "B7 homolog 1"
                ],
                "gene_symbol": "CD274",
                "hgnc_symbol": "CD274",
                "hgnc_release": "2017-11-03",
                "ensembl_genes": {
                    "GRch37": {
                        "82": {
                            "location": "9:5450503-5470566",
                            "ensembl_id": "ENSG00000120217"
                        }
                    },
                    "GRch38": {
                        "90": {
                            "location": "9:5450503-5470566",
                            "ensembl_id": "ENSG00000120217"
                        }
                    }
                },
                "hgnc_date_symbol_changed": "2005-02-25"
            },
            "entity_type": "gene",
            "entity_name": "CD274",
            "confidence_level": "3",
            "penetrance": null,
            "mode_of_pathogenicity": "",
            "publications": [],
            "evidence": [
                "Expert list",
                "Expert Review Green"
            ],
            "phenotypes": [],
            "mode_of_inheritance": "Unknown",
            "tags": [
                "umccr"
            ],
            "panel": {
                "id": 243,
                "hash_id": null,
                "name": "Immune_markers_WTS_UMCCR",
                "disease_group": "Cancer",
                "disease_sub_group": "",
                "description": "Author: Jacek Marzec, jacek.marzec@unimelb.edu.au\r\n\r\nPurpose: panel of immune markers used to assess pre-existing anti-cancer immunity and likelihood of response to immunotherapy. This set of genes is used in UMCCR WTS report \"Immune markers\" section\r\n\r\nSource: https://www.omniseq.com\r\n\r\nGithub: https://github.com/umccr/RNAsum",
                "status": "public",
                "version": "0.77",
                "version_created": "2025-11-03T15:30:48.145923+11:00",
                "relevant_disorders": [],
                "stats": {
                    "number_of_genes": 71,
                    "number_of_strs": 0,
                    "number_of_regions": 0
                },
                "types": [],
                "child_panel_ids": []
            },
            "transcript": null
        },
        {
            "gene_data": {
                "alias": [
                    "S152",
                    "Tp55"
                ],
                "biotype": "protein_coding",
                "hgnc_id": "HGNC:11922",
                "gene_name": "CD27 molecule",
                "omim_gene": [
                    "186711"
                ],
                "alias_name": null,
                "gene_symbol": "CD27",
                "hgnc_symbol": "CD27",
                "hgnc_release": "2017-11-03",
                "ensembl_genes": {
                    "GRch37": {
                        "82": {
                            "location": "12:6554033-6560884",
                            "ensembl_id": "ENSG00000139193"
                        }
                    },
                    "GRch38": {
                        "90": {
                            "location": "12:6444867-6451718",
                            "ensembl_id": "ENSG00000139193"
                        }
                    }
                },
                "hgnc_date_symbol_changed": "2006-10-27"
            },
            "entity_type": "gene",
            "entity_name": "CD27",
            "confidence_level": "3",
            "penetrance": null,
            "mode_of_pathogenicity": "",
            "publications": [],
            "evidence": [
                "Expert list",
                "Expert Review Green"
            ],
            "phenotypes": [],
            "mode_of_inheritance": "Unknown",
            "tags": [
                "umccr"
            ],
            "panel": {
                "id": 243,
                "hash_id": null,
                "name": "Immune_markers_WTS_UMCCR",
                "disease_group": "Cancer",
                "disease_sub_group": "",
                "description": "Author: Jacek Marzec, jacek.marzec@unimelb.edu.au\r\n\r\nPurpose: panel of immune markers used to assess pre-existing anti-cancer immunity and likelihood of response to immunotherapy. This set of genes is used in UMCCR WTS report \"Immune markers\" section\r\n\r\nSource: https://www.omniseq.com\r\n\r\nGithub: https://github.com/umccr/RNAsum",
                "status": "public",
                "version": "0.77",
                "version_created": "2025-11-03T15:30:48.145923+11:00",
                "relevant_disorders": [],
                "stats": {
                    "number_of_genes": 71,
                    "number_of_strs": 0,
                    "number_of_regions": 0
                },
                "types": [],
                "child_panel_ids": []
            },
            "transcript": null
        },
        {
            "gene_data": {
                "alias": [
                    "2B4",
                    "NAIL",
                    "NKR2B4",
                    "Nmrk",
                    "SLAMF4"
                ],
                "biotype": "protein_coding",
                "hgnc_id": "HGNC:18171",
                "gene_name": "CD244 molecule",
                "omim_gene": [
                    "605554"
                ],
                "alias_name": null,
                "gene_symbol": "CD244",
                "hgnc_symbol": "CD244",
                "hgnc_release": "2017-11-03",
                "ensembl_genes": {
                    "GRch37": {
                        "82": {
                            "location": "1:160799950-160832692",
                            "ensembl_id": "ENSG00000122223"
                        }
                    },
                    "GRch38": {
                        "90": {
                            "location": "1:160830160-160862855",
                            "ensembl_id": "ENSG00000122223"
                        }
                    }
                },
                "hgnc_date_symbol_changed": "2003-10-23"
            },
            "entity_type": "gene",
            "entity_name": "CD244",
            "confidence_level": "3",
            "penetrance": null,
            "mode_of_pathogenicity": "",
            "publications": [],
            "evidence": [
                "Expert list",
                "Expert Review Green"
            ],
            "phenotypes": [],
            "mode_of_inheritance": "Unknown",
            "tags": [
                "umccr"
            ],
            "panel": {
                "id": 243,
                "hash_id": null,
                "name": "Immune_markers_WTS_UMCCR",
                "disease_group": "Cancer",
                "disease_sub_group": "",
                "description": "Author: Jacek Marzec, jacek.marzec@unimelb.edu.au\r\n\r\nPurpose: panel of immune markers used to assess pre-existing anti-cancer immunity and likelihood of response to immunotherapy. This set of genes is used in UMCCR WTS report \"Immune markers\" section\r\n\r\nSource: https://www.omniseq.com\r\n\r\nGithub: https://github.com/umccr/RNAsum",
                "status": "public",
                "version": "0.77",
                "version_created": "2025-11-03T15:30:48.145923+11:00",
                "relevant_disorders": [],
                "stats": {
                    "number_of_genes": 71,
                    "number_of_strs": 0,
                    "number_of_regions": 0
                },
                "types": [],
                "child_panel_ids": []
            },
            "transcript": null
        },
        {
            "gene_data": {
                "alias": [
                    "MCD",
                    "hMCD"
                ],
                "biotype": "protein_coding",
                "hgnc_id": "HGNC:7150",
                "gene_name": "malonyl-CoA decarboxylase",
                "omim_gene": [
                    "606761"
                ],
                "alias_name": null,
                "gene_symbol": "MLYCD",
                "hgnc_symbol": "MLYCD",
                "hgnc_release": "2017-11-03",
                "ensembl_genes": {
                    "GRch37": {
                        "82": {
                            "location": "16:83932731-83949787",
                            "ensembl_id": "ENSG00000103150"
                        }
                    },
                    "GRch38": {
                        "90": {
                            "location": "16:83899126-83927026",
                            "ensembl_id": "ENSG00000103150"
                        }
                    }
                },
                "hgnc_date_symbol_changed": "2000-02-11"
            },
            "entity_type": "gene",
            "entity_name": "MLYCD",
            "confidence_level": "3",
            "penetrance": null,
            "mode_of_pathogenicity": "",
            "publications": [
                "12955715"
            ],
            "evidence": [
                "Expert Review Green",
                "Genetic Health Queensland"
            ],
            "phenotypes": [
                "Malonyl-CoA decarboxylase deficiency, MIM# 248360"
            ],
            "mode_of_inheritance": "BIALLELIC, autosomal or pseudoautosomal",
            "tags": [
                "treatable"
            ],
            "panel": {
                "id": 250,
                "hash_id": null,
                "name": "Intellectual disability syndromic and non-syndromic",
                "disease_group": "Neurology and neurodevelopmental disorders",
                "disease_sub_group": "",
                "description": "This panel was created by merging the ID panels used by Genetic Health Queensland and by the Victorian Clinical Genetics Services. Discrepant gene classifications reviewed and resolved by Chirag Patel and Zornitza Stark.\r\n\r\nThis is a consensus panel used by VCGS, GHQ and RMH.\r\n\r\nThis panel has been compared against the Genomics England PanelApp Intellectual Disability panel, and all discrepancies have been resolved, with reciprocal reviews provided to Genomics England, 11/3/2020.",
                "status": "public",
                "version": "1.760",
                "version_created": "2026-04-26T17:50:23.271073+10:00",
                "relevant_disorders": [
                    "Intellectual disability",
                    "HP:0001249; Neurodevelopmental delay",
                    "HP:0012758"
                ],
                "stats": {
                    "number_of_genes": 2524,
                    "number_of_strs": 10,
                    "number_of_regions": 57
                },
                "types": [
                    {
                        "name": "Genetic Health Queensland",
                        "slug": "genetic-health-queensland",
                        "description": "Panel used by GHQ."
                    },
                    {
                        "name": "Victorian Clinical Genetics Services",
                        "slug": "victorian-clinical-genetics-services",
                        "description": "Panel used by VCGS."
                    },
                    {
                        "name": "Rare Disease",
                        "slug": "rare-disease",
                        "description": "Rare disease panels"
                    },
                    {
                        "name": "Royal Melbourne Hospital",
                        "slug": "royal-melbourne-hospital",
                        "description": "Royal Melbourne Hospital"
                    }
                ],
                "child_panel_ids": []
            },
            "transcript": null
        },
        {
            "gene_data": {
                "alias": [
                    "cblA"
                ],
                "biotype": "protein_coding",
                "hgnc_id": "HGNC:18871",
                "gene_name": "methylmalonic aciduria (cobalamin deficiency) cblA type",
                "omim_gene": [
                    "607481"
                ],
                "alias_name": null,
                "gene_symbol": "MMAA",
                "hgnc_symbol": "MMAA",
                "hgnc_release": "2017-11-03",
                "ensembl_genes": {
                    "GRch37": {
                        "82": {
                            "location": "4:146539415-146581187",
                            "ensembl_id": "ENSG00000151611"
                        }
                    },
                    "GRch38": {
                        "90": {
                            "location": "4:145618263-145660035",
                            "ensembl_id": "ENSG00000151611"
                        }
                    }
                },
                "hgnc_date_symbol_changed": "2003-02-11"
            },
            "entity_type": "gene",
            "entity_name": "MMAA",
            "confidence_level": "3",
            "penetrance": null,
            "mode_of_pathogenicity": "",
            "publications": [
                "20301409",
                "37420116"
            ],
            "evidence": [
                "Expert Review Green",
                "Genetic Health Queensland"
            ],
            "phenotypes": [
                "Methylmalonic aciduria, vitamin B12-responsive, cblA type, MIM# 251100"
            ],
            "mode_of_inheritance": "BIALLELIC, autosomal or pseudoautosomal",
            "tags": [
                "treatable"
            ],
            "panel": {
                "id": 250,
                "hash_id": null,
                "name": "Intellectual disability syndromic and non-syndromic",
                "disease_group": "Neurology and neurodevelopmental disorders",
                "disease_sub_group": "",
                "description": "This panel was created by merging the ID panels used by Genetic Health Queensland and by the Victorian Clinical Genetics Services. Discrepant gene classifications reviewed and resolved by Chirag Patel and Zornitza Stark.\r\n\r\nThis is a consensus panel used by VCGS, GHQ and RMH.\r\n\r\nThis panel has been compared against the Genomics England PanelApp Intellectual Disability panel, and all discrepancies have been resolved, with reciprocal reviews provided to Genomics England, 11/3/2020.",
                "status": "public",
                "version": "1.760",
                "version_created": "2026-04-26T17:50:23.271073+10:00",
                "relevant_disorders": [
                    "Intellectual disability",
                    "HP:0001249; Neurodevelopmental delay",
                    "HP:0012758"
                ],
                "stats": {
                    "number_of_genes": 2524,
                    "number_of_strs": 10,
                    "number_of_regions": 57
                },
                "types": [
                    {
                        "name": "Genetic Health Queensland",
                        "slug": "genetic-health-queensland",
                        "description": "Panel used by GHQ."
                    },
                    {
                        "name": "Victorian Clinical Genetics Services",
                        "slug": "victorian-clinical-genetics-services",
                        "description": "Panel used by VCGS."
                    },
                    {
                        "name": "Rare Disease",
                        "slug": "rare-disease",
                        "description": "Rare disease panels"
                    },
                    {
                        "name": "Royal Melbourne Hospital",
                        "slug": "royal-melbourne-hospital",
                        "description": "Royal Melbourne Hospital"
                    }
                ],
                "child_panel_ids": []
            },
            "transcript": null
        },
        {
            "gene_data": {
                "alias": [
                    "cblB",
                    "CFAP23"
                ],
                "biotype": "protein_coding",
                "hgnc_id": "HGNC:19331",
                "gene_name": "methylmalonic aciduria (cobalamin deficiency) cblB type",
                "omim_gene": [
                    "607568"
                ],
                "alias_name": [
                    "ATP:cob(I)alamin adenosyltransferase",
                    "cilia and flagella associated protein 23"
                ],
                "gene_symbol": "MMAB",
                "hgnc_symbol": "MMAB",
                "hgnc_release": "2017-11-03",
                "ensembl_genes": {
                    "GRch37": {
                        "82": {
                            "location": "12:109991542-110011679",
                            "ensembl_id": "ENSG00000139428"
                        }
                    },
                    "GRch38": {
                        "90": {
                            "location": "12:109553737-109573874",
                            "ensembl_id": "ENSG00000139428"
                        }
                    }
                },
                "hgnc_date_symbol_changed": "2003-02-11"
            },
            "entity_type": "gene",
            "entity_name": "MMAB",
            "confidence_level": "3",
            "penetrance": null,
            "mode_of_pathogenicity": "",
            "publications": [
                "20301409",
                "37420116"
            ],
            "evidence": [
                "Expert Review Green",
                "Genetic Health Queensland"
            ],
            "phenotypes": [
                "Methylmalonic aciduria, vitamin B12-responsive, cblB type, MIM# 251110"
            ],
            "mode_of_inheritance": "BIALLELIC, autosomal or pseudoautosomal",
            "tags": [
                "treatable"
            ],
            "panel": {
                "id": 250,
                "hash_id": null,
                "name": "Intellectual disability syndromic and non-syndromic",
                "disease_group": "Neurology and neurodevelopmental disorders",
                "disease_sub_group": "",
                "description": "This panel was created by merging the ID panels used by Genetic Health Queensland and by the Victorian Clinical Genetics Services. Discrepant gene classifications reviewed and resolved by Chirag Patel and Zornitza Stark.\r\n\r\nThis is a consensus panel used by VCGS, GHQ and RMH.\r\n\r\nThis panel has been compared against the Genomics England PanelApp Intellectual Disability panel, and all discrepancies have been resolved, with reciprocal reviews provided to Genomics England, 11/3/2020.",
                "status": "public",
                "version": "1.760",
                "version_created": "2026-04-26T17:50:23.271073+10:00",
                "relevant_disorders": [
                    "Intellectual disability",
                    "HP:0001249; Neurodevelopmental delay",
                    "HP:0012758"
                ],
                "stats": {
                    "number_of_genes": 2524,
                    "number_of_strs": 10,
                    "number_of_regions": 57
                },
                "types": [
                    {
                        "name": "Genetic Health Queensland",
                        "slug": "genetic-health-queensland",
                        "description": "Panel used by GHQ."
                    },
                    {
                        "name": "Victorian Clinical Genetics Services",
                        "slug": "victorian-clinical-genetics-services",
                        "description": "Panel used by VCGS."
                    },
                    {
                        "name": "Rare Disease",
                        "slug": "rare-disease",
                        "description": "Rare disease panels"
                    },
                    {
                        "name": "Royal Melbourne Hospital",
                        "slug": "royal-melbourne-hospital",
                        "description": "Royal Melbourne Hospital"
                    }
                ],
                "child_panel_ids": []
            },
            "transcript": null
        },
        {
            "gene_data": {
                "alias": [
                    "DKFZP564I122",
                    "cblC"
                ],
                "biotype": "protein_coding",
                "hgnc_id": "HGNC:24525",
                "gene_name": "methylmalonic aciduria (cobalamin deficiency) cblC type, with homocystinuria",
                "omim_gene": [
                    "609831"
                ],
                "alias_name": null,
                "gene_symbol": "MMACHC",
                "hgnc_symbol": "MMACHC",
                "hgnc_release": "2017-11-03",
                "ensembl_genes": {
                    "GRch37": {
                        "82": {
                            "location": "1:45965725-45976739",
                            "ensembl_id": "ENSG00000132763"
                        }
                    },
                    "GRch38": {
                        "90": {
                            "location": "1:45500053-45513382",
                            "ensembl_id": "ENSG00000132763"
                        }
                    }
                },
                "hgnc_date_symbol_changed": "2006-01-12"
            },
            "entity_type": "gene",
            "entity_name": "MMACHC",
            "confidence_level": "3",
            "penetrance": null,
            "mode_of_pathogenicity": "",
            "publications": [],
            "evidence": [
                "Expert Review Green",
                "Genetic Health Queensland"
            ],
            "phenotypes": [
                "Methylmalonic aciduria and homocystinuria, cblC type, MIM#277400"
            ],
            "mode_of_inheritance": "BIALLELIC, autosomal or pseudoautosomal",
            "tags": [
                "treatable"
            ],
            "panel": {
                "id": 250,
                "hash_id": null,
                "name": "Intellectual disability syndromic and non-syndromic",
                "disease_group": "Neurology and neurodevelopmental disorders",
                "disease_sub_group": "",
                "description": "This panel was created by merging the ID panels used by Genetic Health Queensland and by the Victorian Clinical Genetics Services. Discrepant gene classifications reviewed and resolved by Chirag Patel and Zornitza Stark.\r\n\r\nThis is a consensus panel used by VCGS, GHQ and RMH.\r\n\r\nThis panel has been compared against the Genomics England PanelApp Intellectual Disability panel, and all discrepancies have been resolved, with reciprocal reviews provided to Genomics England, 11/3/2020.",
                "status": "public",
                "version": "1.760",
                "version_created": "2026-04-26T17:50:23.271073+10:00",
                "relevant_disorders": [
                    "Intellectual disability",
                    "HP:0001249; Neurodevelopmental delay",
                    "HP:0012758"
                ],
                "stats": {
                    "number_of_genes": 2524,
                    "number_of_strs": 10,
                    "number_of_regions": 57
                },
                "types": [
                    {
                        "name": "Genetic Health Queensland",
                        "slug": "genetic-health-queensland",
                        "description": "Panel used by GHQ."
                    },
                    {
                        "name": "Victorian Clinical Genetics Services",
                        "slug": "victorian-clinical-genetics-services",
                        "description": "Panel used by VCGS."
                    },
                    {
                        "name": "Rare Disease",
                        "slug": "rare-disease",
                        "description": "Rare disease panels"
                    },
                    {
                        "name": "Royal Melbourne Hospital",
                        "slug": "royal-melbourne-hospital",
                        "description": "Royal Melbourne Hospital"
                    }
                ],
                "child_panel_ids": []
            },
            "transcript": null
        },
        {
            "gene_data": {
                "alias": [
                    "CL25022",
                    "cblD"
                ],
                "biotype": "protein_coding",
                "hgnc_id": "HGNC:25221",
                "gene_name": "methylmalonic aciduria and homocystinuria, cblD type",
                "omim_gene": [
                    "611935"
                ],
                "alias_name": null,
                "gene_symbol": "MMADHC",
                "hgnc_symbol": "MMADHC",
                "hgnc_release": "2017-11-03",
                "ensembl_genes": {
                    "GRch37": {
                        "82": {
                            "location": "2:150426148-150444330",
                            "ensembl_id": "ENSG00000168288"
                        }
                    },
                    "GRch38": {
                        "90": {
                            "location": "2:149569634-149587816",
                            "ensembl_id": "ENSG00000168288"
                        }
                    }
                },
                "hgnc_date_symbol_changed": "2009-01-08"
            },
            "entity_type": "gene",
            "entity_name": "MMADHC",
            "confidence_level": "3",
            "penetrance": null,
            "mode_of_pathogenicity": "",
            "publications": [
                "20301409",
                "37420116",
                "27604308",
                "18385497"
            ],
            "evidence": [
                "Expert Review Green",
                "Genetic Health Queensland"
            ],
            "phenotypes": [
                "Homocystinuria, cblD type, variant 1 MIM#277410",
                "Methylmalonic aciduria and homocystinuria, cblD type MIM#277410",
                "Methylmalonic aciduria, cblD type, variant 2 MIM#277410",
                "Disorders of cobalamin absorption, transport and metabolism"
            ],
            "mode_of_inheritance": "BIALLELIC, autosomal or pseudoautosomal",
            "tags": [
                "treatable"
            ],
            "panel": {
                "id": 250,
                "hash_id": null,
                "name": "Intellectual disability syndromic and non-syndromic",
                "disease_group": "Neurology and neurodevelopmental disorders",
                "disease_sub_group": "",
                "description": "This panel was created by merging the ID panels used by Genetic Health Queensland and by the Victorian Clinical Genetics Services. Discrepant gene classifications reviewed and resolved by Chirag Patel and Zornitza Stark.\r\n\r\nThis is a consensus panel used by VCGS, GHQ and RMH.\r\n\r\nThis panel has been compared against the Genomics England PanelApp Intellectual Disability panel, and all discrepancies have been resolved, with reciprocal reviews provided to Genomics England, 11/3/2020.",
                "status": "public",
                "version": "1.760",
                "version_created": "2026-04-26T17:50:23.271073+10:00",
                "relevant_disorders": [
                    "Intellectual disability",
                    "HP:0001249; Neurodevelopmental delay",
                    "HP:0012758"
                ],
                "stats": {
                    "number_of_genes": 2524,
                    "number_of_strs": 10,
                    "number_of_regions": 57
                },
                "types": [
                    {
                        "name": "Genetic Health Queensland",
                        "slug": "genetic-health-queensland",
                        "description": "Panel used by GHQ."
                    },
                    {
                        "name": "Victorian Clinical Genetics Services",
                        "slug": "victorian-clinical-genetics-services",
                        "description": "Panel used by VCGS."
                    },
                    {
                        "name": "Rare Disease",
                        "slug": "rare-disease",
                        "description": "Rare disease panels"
                    },
                    {
                        "name": "Royal Melbourne Hospital",
                        "slug": "royal-melbourne-hospital",
                        "description": "Royal Melbourne Hospital"
                    }
                ],
                "child_panel_ids": []
            },
            "transcript": null
        },
        {
            "gene_data": {
                "alias": [
                    "HB9",
                    "HOXHB9",
                    "SCRA1"
                ],
                "biotype": "protein_coding",
                "hgnc_id": "HGNC:4979",
                "gene_name": "motor neuron and pancreas homeobox 1",
                "omim_gene": [
                    "142994"
                ],
                "alias_name": null,
                "gene_symbol": "MNX1",
                "hgnc_symbol": "MNX1",
                "hgnc_release": "2017-11-03",
                "ensembl_genes": {
                    "GRch37": {
                        "82": {
                            "location": "7:156786745-156803345",
                            "ensembl_id": "ENSG00000130675"
                        }
                    },
                    "GRch38": {
                        "90": {
                            "location": "7:156994051-157010651",
                            "ensembl_id": "ENSG00000130675"
                        }
                    }
                },
                "hgnc_date_symbol_changed": "2007-08-09"
            },
            "entity_type": "gene",
            "entity_name": "MNX1",
            "confidence_level": "1",
            "penetrance": null,
            "mode_of_pathogenicity": "",
            "publications": [],
            "evidence": [
                "Expert Review Red",
                "Expert list"
            ],
            "phenotypes": [
                "Currarino syndrome",
                "OMIM #176450"
            ],
            "mode_of_inheritance": "MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted",
            "tags": [],
            "panel": {
                "id": 250,
                "hash_id": null,
                "name": "Intellectual disability syndromic and non-syndromic",
                "disease_group": "Neurology and neurodevelopmental disorders",
                "disease_sub_group": "",
                "description": "This panel was created by merging the ID panels used by Genetic Health Queensland and by the Victorian Clinical Genetics Services. Discrepant gene classifications reviewed and resolved by Chirag Patel and Zornitza Stark.\r\n\r\nThis is a consensus panel used by VCGS, GHQ and RMH.\r\n\r\nThis panel has been compared against the Genomics England PanelApp Intellectual Disability panel, and all discrepancies have been resolved, with reciprocal reviews provided to Genomics England, 11/3/2020.",
                "status": "public",
                "version": "1.760",
                "version_created": "2026-04-26T17:50:23.271073+10:00",
                "relevant_disorders": [
                    "Intellectual disability",
                    "HP:0001249; Neurodevelopmental delay",
                    "HP:0012758"
                ],
                "stats": {
                    "number_of_genes": 2524,
                    "number_of_strs": 10,
                    "number_of_regions": 57
                },
                "types": [
                    {
                        "name": "Genetic Health Queensland",
                        "slug": "genetic-health-queensland",
                        "description": "Panel used by GHQ."
                    },
                    {
                        "name": "Victorian Clinical Genetics Services",
                        "slug": "victorian-clinical-genetics-services",
                        "description": "Panel used by VCGS."
                    },
                    {
                        "name": "Rare Disease",
                        "slug": "rare-disease",
                        "description": "Rare disease panels"
                    },
                    {
                        "name": "Royal Melbourne Hospital",
                        "slug": "royal-melbourne-hospital",
                        "description": "Royal Melbourne Hospital"
                    }
                ],
                "child_panel_ids": []
            },
            "transcript": null
        },
        {
            "gene_data": {
                "alias": [
                    "MOCOD"
                ],
                "biotype": "protein_coding",
                "hgnc_id": "HGNC:7190",
                "gene_name": "molybdenum cofactor synthesis 1",
                "omim_gene": [
                    "603707"
                ],
                "alias_name": null,
                "gene_symbol": "MOCS1",
                "hgnc_symbol": "MOCS1",
                "hgnc_release": "2017-11-03",
                "ensembl_genes": {
                    "GRch37": {
                        "82": {
                            "location": "6:39867354-39902290",
                            "ensembl_id": "ENSG00000124615"
                        }
                    },
                    "GRch38": {
                        "90": {
                            "location": "6:39899578-39934551",
                            "ensembl_id": "ENSG00000124615"
                        }
                    }
                },
                "hgnc_date_symbol_changed": "1998-07-23"
            },
            "entity_type": "gene",
            "entity_name": "MOCS1",
            "confidence_level": "3",
            "penetrance": null,
            "mode_of_pathogenicity": "",
            "publications": [
                "9921896",
                "12754701",
                "21031595"
            ],
            "evidence": [
                "Expert Review Green",
                "Genetic Health Queensland"
            ],
            "phenotypes": [
                "Molybdenum cofactor deficiency A, MIM# 252150"
            ],
            "mode_of_inheritance": "BIALLELIC, autosomal or pseudoautosomal",
            "tags": [
                "treatable"
            ],
            "panel": {
                "id": 250,
                "hash_id": null,
                "name": "Intellectual disability syndromic and non-syndromic",
                "disease_group": "Neurology and neurodevelopmental disorders",
                "disease_sub_group": "",
                "description": "This panel was created by merging the ID panels used by Genetic Health Queensland and by the Victorian Clinical Genetics Services. Discrepant gene classifications reviewed and resolved by Chirag Patel and Zornitza Stark.\r\n\r\nThis is a consensus panel used by VCGS, GHQ and RMH.\r\n\r\nThis panel has been compared against the Genomics England PanelApp Intellectual Disability panel, and all discrepancies have been resolved, with reciprocal reviews provided to Genomics England, 11/3/2020.",
                "status": "public",
                "version": "1.760",
                "version_created": "2026-04-26T17:50:23.271073+10:00",
                "relevant_disorders": [
                    "Intellectual disability",
                    "HP:0001249; Neurodevelopmental delay",
                    "HP:0012758"
                ],
                "stats": {
                    "number_of_genes": 2524,
                    "number_of_strs": 10,
                    "number_of_regions": 57
                },
                "types": [
                    {
                        "name": "Genetic Health Queensland",
                        "slug": "genetic-health-queensland",
                        "description": "Panel used by GHQ."
                    },
                    {
                        "name": "Victorian Clinical Genetics Services",
                        "slug": "victorian-clinical-genetics-services",
                        "description": "Panel used by VCGS."
                    },
                    {
                        "name": "Rare Disease",
                        "slug": "rare-disease",
                        "description": "Rare disease panels"
                    },
                    {
                        "name": "Royal Melbourne Hospital",
                        "slug": "royal-melbourne-hospital",
                        "description": "Royal Melbourne Hospital"
                    }
                ],
                "child_panel_ids": []
            },
            "transcript": null
        },
        {
            "gene_data": {
                "alias": [
                    "MOCO1"
                ],
                "biotype": "protein_coding",
                "hgnc_id": "HGNC:7193",
                "gene_name": "molybdenum cofactor synthesis 2",
                "omim_gene": [
                    "603708"
                ],
                "alias_name": null,
                "gene_symbol": "MOCS2",
                "hgnc_symbol": "MOCS2",
                "hgnc_release": "2017-11-03",
                "ensembl_genes": {
                    "GRch37": {
                        "82": {
                            "location": "5:52391509-52405893",
                            "ensembl_id": "ENSG00000164172"
                        }
                    },
                    "GRch38": {
                        "90": {
                            "location": "5:53095679-53110063",
                            "ensembl_id": "ENSG00000164172"
                        }
                    }
                },
                "hgnc_date_symbol_changed": "1998-07-23"
            },
            "entity_type": "gene",
            "entity_name": "MOCS2",
            "confidence_level": "3",
            "penetrance": null,
            "mode_of_pathogenicity": "",
            "publications": [
                "27604308",
                "10053004"
            ],
            "evidence": [
                "Expert Review Green",
                "Genetic Health Queensland"
            ],
            "phenotypes": [
                "Molybdenum cofactor deficiency B MIM#252160",
                "Disorders of molybdenum cofactor metabolism"
            ],
            "mode_of_inheritance": "BIALLELIC, autosomal or pseudoautosomal",
            "tags": [],
            "panel": {
                "id": 250,
                "hash_id": null,
                "name": "Intellectual disability syndromic and non-syndromic",
                "disease_group": "Neurology and neurodevelopmental disorders",
                "disease_sub_group": "",
                "description": "This panel was created by merging the ID panels used by Genetic Health Queensland and by the Victorian Clinical Genetics Services. Discrepant gene classifications reviewed and resolved by Chirag Patel and Zornitza Stark.\r\n\r\nThis is a consensus panel used by VCGS, GHQ and RMH.\r\n\r\nThis panel has been compared against the Genomics England PanelApp Intellectual Disability panel, and all discrepancies have been resolved, with reciprocal reviews provided to Genomics England, 11/3/2020.",
                "status": "public",
                "version": "1.760",
                "version_created": "2026-04-26T17:50:23.271073+10:00",
                "relevant_disorders": [
                    "Intellectual disability",
                    "HP:0001249; Neurodevelopmental delay",
                    "HP:0012758"
                ],
                "stats": {
                    "number_of_genes": 2524,
                    "number_of_strs": 10,
                    "number_of_regions": 57
                },
                "types": [
                    {
                        "name": "Genetic Health Queensland",
                        "slug": "genetic-health-queensland",
                        "description": "Panel used by GHQ."
                    },
                    {
                        "name": "Victorian Clinical Genetics Services",
                        "slug": "victorian-clinical-genetics-services",
                        "description": "Panel used by VCGS."
                    },
                    {
                        "name": "Rare Disease",
                        "slug": "rare-disease",
                        "description": "Rare disease panels"
                    },
                    {
                        "name": "Royal Melbourne Hospital",
                        "slug": "royal-melbourne-hospital",
                        "description": "Royal Melbourne Hospital"
                    }
                ],
                "child_panel_ids": []
            },
            "transcript": null
        },
        {
            "gene_data": {
                "alias": [
                    "GCS1",
                    "CWH41",
                    "DER7"
                ],
                "biotype": "protein_coding",
                "hgnc_id": "HGNC:24862",
                "gene_name": "mannosyl-oligosaccharide glucosidase",
                "omim_gene": [
                    "601336"
                ],
                "alias_name": [
                    "glucosidase I",
                    "processing A-glucosidase I"
                ],
                "gene_symbol": "MOGS",
                "hgnc_symbol": "MOGS",
                "hgnc_release": "2017-11-03",
                "ensembl_genes": {
                    "GRch37": {
                        "82": {
                            "location": "2:74688184-74692537",
                            "ensembl_id": "ENSG00000115275"
                        }
                    },
                    "GRch38": {
                        "90": {
                            "location": "2:74461057-74465410",
                            "ensembl_id": "ENSG00000115275"
                        }
                    }
                },
                "hgnc_date_symbol_changed": "2009-03-24"
            },
            "entity_type": "gene",
            "entity_name": "MOGS",
            "confidence_level": "3",
            "penetrance": null,
            "mode_of_pathogenicity": "",
            "publications": [
                "31925597",
                "30587846",
                "33058492"
            ],
            "evidence": [
                "Expert Review Green",
                "Genetic Health Queensland"
            ],
            "phenotypes": [
                "Congenital disorder of glycosylation, type IIb, MIM# 606056"
            ],
            "mode_of_inheritance": "BIALLELIC, autosomal or pseudoautosomal",
            "tags": [],
            "panel": {
                "id": 250,
                "hash_id": null,
                "name": "Intellectual disability syndromic and non-syndromic",
                "disease_group": "Neurology and neurodevelopmental disorders",
                "disease_sub_group": "",
                "description": "This panel was created by merging the ID panels used by Genetic Health Queensland and by the Victorian Clinical Genetics Services. Discrepant gene classifications reviewed and resolved by Chirag Patel and Zornitza Stark.\r\n\r\nThis is a consensus panel used by VCGS, GHQ and RMH.\r\n\r\nThis panel has been compared against the Genomics England PanelApp Intellectual Disability panel, and all discrepancies have been resolved, with reciprocal reviews provided to Genomics England, 11/3/2020.",
                "status": "public",
                "version": "1.760",
                "version_created": "2026-04-26T17:50:23.271073+10:00",
                "relevant_disorders": [
                    "Intellectual disability",
                    "HP:0001249; Neurodevelopmental delay",
                    "HP:0012758"
                ],
                "stats": {
                    "number_of_genes": 2524,
                    "number_of_strs": 10,
                    "number_of_regions": 57
                },
                "types": [
                    {
                        "name": "Genetic Health Queensland",
                        "slug": "genetic-health-queensland",
                        "description": "Panel used by GHQ."
                    },
                    {
                        "name": "Victorian Clinical Genetics Services",
                        "slug": "victorian-clinical-genetics-services",
                        "description": "Panel used by VCGS."
                    },
                    {
                        "name": "Rare Disease",
                        "slug": "rare-disease",
                        "description": "Rare disease panels"
                    },
                    {
                        "name": "Royal Melbourne Hospital",
                        "slug": "royal-melbourne-hospital",
                        "description": "Royal Melbourne Hospital"
                    }
                ],
                "child_panel_ids": []
            },
            "transcript": null
        },
        {
            "gene_data": {
                "alias": [
                    "SL15",
                    "Lec35",
                    "PQLC5",
                    "CDGIf"
                ],
                "biotype": "protein_coding",
                "hgnc_id": "HGNC:7207",
                "gene_name": "mannose-P-dolichol utilization defect 1",
                "omim_gene": [
                    "604041"
                ],
                "alias_name": null,
                "gene_symbol": "MPDU1",
                "hgnc_symbol": "MPDU1",
                "hgnc_release": "2017-11-03",
                "ensembl_genes": {
                    "GRch37": {
                        "82": {
                            "location": "17:7486847-7496107",
                            "ensembl_id": "ENSG00000129255"
                        }
                    },
                    "GRch38": {
                        "90": {
                            "location": "17:7583529-7592789",
                            "ensembl_id": "ENSG00000129255"
                        }
                    }
                },
                "hgnc_date_symbol_changed": "1999-05-25"
            },
            "entity_type": "gene",
            "entity_name": "MPDU1",
            "confidence_level": "3",
            "penetrance": null,
            "mode_of_pathogenicity": "",
            "publications": [
                "11733564",
                "11733556",
                "31741824",
                "29721919"
            ],
            "evidence": [
                "Expert Review Green",
                "Genetic Health Queensland"
            ],
            "phenotypes": [
                "Congenital disorder of glycosylation, type If, MIM# 609180",
                "MPDU1-CDG, MONDO:0012211"
            ],
            "mode_of_inheritance": "BIALLELIC, autosomal or pseudoautosomal",
            "tags": [],
            "panel": {
                "id": 250,
                "hash_id": null,
                "name": "Intellectual disability syndromic and non-syndromic",
                "disease_group": "Neurology and neurodevelopmental disorders",
                "disease_sub_group": "",
                "description": "This panel was created by merging the ID panels used by Genetic Health Queensland and by the Victorian Clinical Genetics Services. Discrepant gene classifications reviewed and resolved by Chirag Patel and Zornitza Stark.\r\n\r\nThis is a consensus panel used by VCGS, GHQ and RMH.\r\n\r\nThis panel has been compared against the Genomics England PanelApp Intellectual Disability panel, and all discrepancies have been resolved, with reciprocal reviews provided to Genomics England, 11/3/2020.",
                "status": "public",
                "version": "1.760",
                "version_created": "2026-04-26T17:50:23.271073+10:00",
                "relevant_disorders": [
                    "Intellectual disability",
                    "HP:0001249; Neurodevelopmental delay",
                    "HP:0012758"
                ],
                "stats": {
                    "number_of_genes": 2524,
                    "number_of_strs": 10,
                    "number_of_regions": 57
                },
                "types": [
                    {
                        "name": "Genetic Health Queensland",
                        "slug": "genetic-health-queensland",
                        "description": "Panel used by GHQ."
                    },
                    {
                        "name": "Victorian Clinical Genetics Services",
                        "slug": "victorian-clinical-genetics-services",
                        "description": "Panel used by VCGS."
                    },
                    {
                        "name": "Rare Disease",
                        "slug": "rare-disease",
                        "description": "Rare disease panels"
                    },
                    {
                        "name": "Royal Melbourne Hospital",
                        "slug": "royal-melbourne-hospital",
                        "description": "Royal Melbourne Hospital"
                    }
                ],
                "child_panel_ids": []
            },
            "transcript": null
        },
        {
            "gene_data": {
                "alias": [
                    "MUPP1"
                ],
                "biotype": "protein_coding",
                "hgnc_id": "HGNC:7208",
                "gene_name": "multiple PDZ domain crumbs cell polarity complex component",
                "omim_gene": [
                    "603785"
                ],
                "alias_name": null,
                "gene_symbol": "MPDZ",
                "hgnc_symbol": "MPDZ",
                "hgnc_release": "2017-11-03",
                "ensembl_genes": {
                    "GRch37": {
                        "82": {
                            "location": "9:13105703-13279589",
                            "ensembl_id": "ENSG00000107186"
                        }
                    },
                    "GRch38": {
                        "90": {
                            "location": "9:13105704-13279590",
                            "ensembl_id": "ENSG00000107186"
                        }
                    }
                },
                "hgnc_date_symbol_changed": "1998-12-16"
            },
            "entity_type": "gene",
            "entity_name": "MPDZ",
            "confidence_level": "3",
            "penetrance": null,
            "mode_of_pathogenicity": "",
            "publications": [
                "PubMed: 28556411",
                "23240096"
            ],
            "evidence": [
                "Expert Review Green",
                "Expert list"
            ],
            "phenotypes": [
                "Hydrocephalus, congenital, 2, with or without brain or eye anomalies",
                "OMIM #615219"
            ],
            "mode_of_inheritance": "BIALLELIC, autosomal or pseudoautosomal",
            "tags": [],
            "panel": {
                "id": 250,
                "hash_id": null,
                "name": "Intellectual disability syndromic and non-syndromic",
                "disease_group": "Neurology and neurodevelopmental disorders",
                "disease_sub_group": "",
                "description": "This panel was created by merging the ID panels used by Genetic Health Queensland and by the Victorian Clinical Genetics Services. Discrepant gene classifications reviewed and resolved by Chirag Patel and Zornitza Stark.\r\n\r\nThis is a consensus panel used by VCGS, GHQ and RMH.\r\n\r\nThis panel has been compared against the Genomics England PanelApp Intellectual Disability panel, and all discrepancies have been resolved, with reciprocal reviews provided to Genomics England, 11/3/2020.",
                "status": "public",
                "version": "1.760",
                "version_created": "2026-04-26T17:50:23.271073+10:00",
                "relevant_disorders": [
                    "Intellectual disability",
                    "HP:0001249; Neurodevelopmental delay",
                    "HP:0012758"
                ],
                "stats": {
                    "number_of_genes": 2524,
                    "number_of_strs": 10,
                    "number_of_regions": 57
                },
                "types": [
                    {
                        "name": "Genetic Health Queensland",
                        "slug": "genetic-health-queensland",
                        "description": "Panel used by GHQ."
                    },
                    {
                        "name": "Victorian Clinical Genetics Services",
                        "slug": "victorian-clinical-genetics-services",
                        "description": "Panel used by VCGS."
                    },
                    {
                        "name": "Rare Disease",
                        "slug": "rare-disease",
                        "description": "Rare disease panels"
                    },
                    {
                        "name": "Royal Melbourne Hospital",
                        "slug": "royal-melbourne-hospital",
                        "description": "Royal Melbourne Hospital"
                    }
                ],
                "child_panel_ids": []
            },
            "transcript": null
        },
        {
            "gene_data": {
                "alias": [],
                "biotype": "protein_coding",
                "hgnc_id": "HGNC:7216",
                "gene_name": "mannose phosphate isomerase",
                "omim_gene": [
                    "154550"
                ],
                "alias_name": [
                    "mannose-6-phosphate isomerase"
                ],
                "gene_symbol": "MPI",
                "hgnc_symbol": "MPI",
                "hgnc_release": "2017-11-03",
                "ensembl_genes": {
                    "GRch37": {
                        "82": {
                            "location": "15:75182346-75191798",
                            "ensembl_id": "ENSG00000178802"
                        }
                    },
                    "GRch38": {
                        "90": {
                            "location": "15:74890005-74902219",
                            "ensembl_id": "ENSG00000178802"
                        }
                    }
                },
                "hgnc_date_symbol_changed": "2001-06-22"
            },
            "entity_type": "gene",
            "entity_name": "MPI",
            "confidence_level": "1",
            "penetrance": null,
            "mode_of_pathogenicity": "",
            "publications": [
                "12414827",
                "9585601",
                "10980531",
                "33098580",
                "33204592",
                "32905087",
                "32266963",
                "30242110"
            ],
            "evidence": [
                "Expert Review Red",
                "Genetic Health Queensland"
            ],
            "phenotypes": [
                "Congenital disorder of glycosylation, type Ib, MIM# 602579",
                "MPI-CDG MONDO:0011257"
            ],
            "mode_of_inheritance": "BIALLELIC, autosomal or pseudoautosomal",
            "tags": [],
            "panel": {
                "id": 250,
                "hash_id": null,
                "name": "Intellectual disability syndromic and non-syndromic",
                "disease_group": "Neurology and neurodevelopmental disorders",
                "disease_sub_group": "",
                "description": "This panel was created by merging the ID panels used by Genetic Health Queensland and by the Victorian Clinical Genetics Services. Discrepant gene classifications reviewed and resolved by Chirag Patel and Zornitza Stark.\r\n\r\nThis is a consensus panel used by VCGS, GHQ and RMH.\r\n\r\nThis panel has been compared against the Genomics England PanelApp Intellectual Disability panel, and all discrepancies have been resolved, with reciprocal reviews provided to Genomics England, 11/3/2020.",
                "status": "public",
                "version": "1.760",
                "version_created": "2026-04-26T17:50:23.271073+10:00",
                "relevant_disorders": [
                    "Intellectual disability",
                    "HP:0001249; Neurodevelopmental delay",
                    "HP:0012758"
                ],
                "stats": {
                    "number_of_genes": 2524,
                    "number_of_strs": 10,
                    "number_of_regions": 57
                },
                "types": [
                    {
                        "name": "Genetic Health Queensland",
                        "slug": "genetic-health-queensland",
                        "description": "Panel used by GHQ."
                    },
                    {
                        "name": "Victorian Clinical Genetics Services",
                        "slug": "victorian-clinical-genetics-services",
                        "description": "Panel used by VCGS."
                    },
                    {
                        "name": "Rare Disease",
                        "slug": "rare-disease",
                        "description": "Rare disease panels"
                    },
                    {
                        "name": "Royal Melbourne Hospital",
                        "slug": "royal-melbourne-hospital",
                        "description": "Royal Melbourne Hospital"
                    }
                ],
                "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"
                        }
                    }
                },
                "hgnc_date_symbol_changed": "2012-03-01"
            },
            "entity_type": "gene",
            "entity_name": "MPLKIP",
            "confidence_level": "3",
            "penetrance": null,
            "mode_of_pathogenicity": "",
            "publications": [
                "15645389",
                "16977596"
            ],
            "evidence": [
                "Expert Review Green",
                "Genetic Health Queensland"
            ],
            "phenotypes": [
                "Trichothiodystrophy 4, nonphotosensitive, MIM# 234050",
                "MONDO:0021013"
            ],
            "mode_of_inheritance": "BIALLELIC, autosomal or pseudoautosomal",
            "tags": [],
            "panel": {
                "id": 250,
                "hash_id": null,
                "name": "Intellectual disability syndromic and non-syndromic",
                "disease_group": "Neurology and neurodevelopmental disorders",
                "disease_sub_group": "",
                "description": "This panel was created by merging the ID panels used by Genetic Health Queensland and by the Victorian Clinical Genetics Services. Discrepant gene classifications reviewed and resolved by Chirag Patel and Zornitza Stark.\r\n\r\nThis is a consensus panel used by VCGS, GHQ and RMH.\r\n\r\nThis panel has been compared against the Genomics England PanelApp Intellectual Disability panel, and all discrepancies have been resolved, with reciprocal reviews provided to Genomics England, 11/3/2020.",
                "status": "public",
                "version": "1.760",
                "version_created": "2026-04-26T17:50:23.271073+10:00",
                "relevant_disorders": [
                    "Intellectual disability",
                    "HP:0001249; Neurodevelopmental delay",
                    "HP:0012758"
                ],
                "stats": {
                    "number_of_genes": 2524,
                    "number_of_strs": 10,
                    "number_of_regions": 57
                },
                "types": [
                    {
                        "name": "Genetic Health Queensland",
                        "slug": "genetic-health-queensland",
                        "description": "Panel used by GHQ."
                    },
                    {
                        "name": "Victorian Clinical Genetics Services",
                        "slug": "victorian-clinical-genetics-services",
                        "description": "Panel used by VCGS."
                    },
                    {
                        "name": "Rare Disease",
                        "slug": "rare-disease",
                        "description": "Rare disease panels"
                    },
                    {
                        "name": "Royal Melbourne Hospital",
                        "slug": "royal-melbourne-hospital",
                        "description": "Royal Melbourne Hospital"
                    }
                ],
                "child_panel_ids": []
            },
            "transcript": null
        },
        {
            "gene_data": {
                "alias": [
                    "SYM1"
                ],
                "biotype": "protein_coding",
                "hgnc_id": "HGNC:7224",
                "gene_name": "MPV17, mitochondrial inner membrane protein",
                "omim_gene": [
                    "137960"
                ],
                "alias_name": [
                    "glomerulosclerosis"
                ],
                "gene_symbol": "MPV17",
                "hgnc_symbol": "MPV17",
                "hgnc_release": "2017-11-03",
                "ensembl_genes": {
                    "GRch37": {
                        "82": {
                            "location": "2:27532360-27548547",
                            "ensembl_id": "ENSG00000115204"
                        }
                    },
                    "GRch38": {
                        "90": {
                            "location": "2:27309492-27325680",
                            "ensembl_id": "ENSG00000115204"
                        }
                    }
                },
                "hgnc_date_symbol_changed": "1994-03-21"
            },
            "entity_type": "gene",
            "entity_name": "MPV17",
            "confidence_level": "3",
            "penetrance": null,
            "mode_of_pathogenicity": "",
            "publications": [
                "PMID: 22593919"
            ],
            "evidence": [
                "Expert Review Green",
                "Expert list"
            ],
            "phenotypes": [
                "Charcot-Marie-Tooth disease, axonal, type 2EE, OMIM #618400",
                "Mitochondrial DNA depletion syndrome 6 (hepatocerebral type), OMIM #256810"
            ],
            "mode_of_inheritance": "BIALLELIC, autosomal or pseudoautosomal",
            "tags": [],
            "panel": {
                "id": 250,
                "hash_id": null,
                "name": "Intellectual disability syndromic and non-syndromic",
                "disease_group": "Neurology and neurodevelopmental disorders",
                "disease_sub_group": "",
                "description": "This panel was created by merging the ID panels used by Genetic Health Queensland and by the Victorian Clinical Genetics Services. Discrepant gene classifications reviewed and resolved by Chirag Patel and Zornitza Stark.\r\n\r\nThis is a consensus panel used by VCGS, GHQ and RMH.\r\n\r\nThis panel has been compared against the Genomics England PanelApp Intellectual Disability panel, and all discrepancies have been resolved, with reciprocal reviews provided to Genomics England, 11/3/2020.",
                "status": "public",
                "version": "1.760",
                "version_created": "2026-04-26T17:50:23.271073+10:00",
                "relevant_disorders": [
                    "Intellectual disability",
                    "HP:0001249; Neurodevelopmental delay",
                    "HP:0012758"
                ],
                "stats": {
                    "number_of_genes": 2524,
                    "number_of_strs": 10,
                    "number_of_regions": 57
                },
                "types": [
                    {
                        "name": "Genetic Health Queensland",
                        "slug": "genetic-health-queensland",
                        "description": "Panel used by GHQ."
                    },
                    {
                        "name": "Victorian Clinical Genetics Services",
                        "slug": "victorian-clinical-genetics-services",
                        "description": "Panel used by VCGS."
                    },
                    {
                        "name": "Rare Disease",
                        "slug": "rare-disease",
                        "description": "Rare disease panels"
                    },
                    {
                        "name": "Royal Melbourne Hospital",
                        "slug": "royal-melbourne-hospital",
                        "description": "Royal Melbourne Hospital"
                    }
                ],
                "child_panel_ids": []
            },
            "transcript": null
        },
        {
            "gene_data": {
                "alias": [
                    "HMSNIB",
                    "CMT2I",
                    "CMT2J"
                ],
                "biotype": "protein_coding",
                "hgnc_id": "HGNC:7225",
                "gene_name": "myelin protein zero",
                "omim_gene": [
                    "159440"
                ],
                "alias_name": null,
                "gene_symbol": "MPZ",
                "hgnc_symbol": "MPZ",
                "hgnc_release": "2017-11-03",
                "ensembl_genes": {
                    "GRch37": {
                        "82": {
                            "location": "1:161274525-161279762",
                            "ensembl_id": "ENSG00000158887"
                        }
                    },
                    "GRch38": {
                        "90": {
                            "location": "1:161304735-161309972",
                            "ensembl_id": "ENSG00000158887"
                        }
                    }
                },
                "hgnc_date_symbol_changed": "1990-04-27"
            },
            "entity_type": "gene",
            "entity_name": "MPZ",
            "confidence_level": "1",
            "penetrance": null,
            "mode_of_pathogenicity": "",
            "publications": [],
            "evidence": [
                "Expert Review Red",
                "Expert list"
            ],
            "phenotypes": [
                "Various CMT types"
            ],
            "mode_of_inheritance": "BOTH monoallelic and biallelic (but BIALLELIC mutations cause a more SEVERE disease form), autosomal or pseudoautosomal",
            "tags": [],
            "panel": {
                "id": 250,
                "hash_id": null,
                "name": "Intellectual disability syndromic and non-syndromic",
                "disease_group": "Neurology and neurodevelopmental disorders",
                "disease_sub_group": "",
                "description": "This panel was created by merging the ID panels used by Genetic Health Queensland and by the Victorian Clinical Genetics Services. Discrepant gene classifications reviewed and resolved by Chirag Patel and Zornitza Stark.\r\n\r\nThis is a consensus panel used by VCGS, GHQ and RMH.\r\n\r\nThis panel has been compared against the Genomics England PanelApp Intellectual Disability panel, and all discrepancies have been resolved, with reciprocal reviews provided to Genomics England, 11/3/2020.",
                "status": "public",
                "version": "1.760",
                "version_created": "2026-04-26T17:50:23.271073+10:00",
                "relevant_disorders": [
                    "Intellectual disability",
                    "HP:0001249; Neurodevelopmental delay",
                    "HP:0012758"
                ],
                "stats": {
                    "number_of_genes": 2524,
                    "number_of_strs": 10,
                    "number_of_regions": 57
                },
                "types": [
                    {
                        "name": "Genetic Health Queensland",
                        "slug": "genetic-health-queensland",
                        "description": "Panel used by GHQ."
                    },
                    {
                        "name": "Victorian Clinical Genetics Services",
                        "slug": "victorian-clinical-genetics-services",
                        "description": "Panel used by VCGS."
                    },
                    {
                        "name": "Rare Disease",
                        "slug": "rare-disease",
                        "description": "Rare disease panels"
                    },
                    {
                        "name": "Royal Melbourne Hospital",
                        "slug": "royal-melbourne-hospital",
                        "description": "Royal Melbourne Hospital"
                    }
                ],
                "child_panel_ids": []
            },
            "transcript": null
        },
        {
            "gene_data": {
                "alias": [
                    "B27",
                    "FALP"
                ],
                "biotype": "protein_coding",
                "hgnc_id": "HGNC:1304",
                "gene_name": "melanocortin 2 receptor accessory protein",
                "omim_gene": [
                    "609196"
                ],
                "alias_name": null,
                "gene_symbol": "MRAP",
                "hgnc_symbol": "MRAP",
                "hgnc_release": "2017-11-03",
                "ensembl_genes": {
                    "GRch37": {
                        "82": {
                            "location": "21:33664124-33687095",
                            "ensembl_id": "ENSG00000170262"
                        }
                    },
                    "GRch38": {
                        "90": {
                            "location": "21:32291813-32314784",
                            "ensembl_id": "ENSG00000170262"
                        }
                    }
                },
                "hgnc_date_symbol_changed": "2005-02-07"
            },
            "entity_type": "gene",
            "entity_name": "MRAP",
            "confidence_level": "1",
            "penetrance": null,
            "mode_of_pathogenicity": "",
            "publications": [],
            "evidence": [
                "Expert Review Red",
                "Expert list"
            ],
            "phenotypes": [
                "Glucocorticoid deficiency 2",
                "OMIM #607398"
            ],
            "mode_of_inheritance": "BIALLELIC, autosomal or pseudoautosomal",
            "tags": [],
            "panel": {
                "id": 250,
                "hash_id": null,
                "name": "Intellectual disability syndromic and non-syndromic",
                "disease_group": "Neurology and neurodevelopmental disorders",
                "disease_sub_group": "",
                "description": "This panel was created by merging the ID panels used by Genetic Health Queensland and by the Victorian Clinical Genetics Services. Discrepant gene classifications reviewed and resolved by Chirag Patel and Zornitza Stark.\r\n\r\nThis is a consensus panel used by VCGS, GHQ and RMH.\r\n\r\nThis panel has been compared against the Genomics England PanelApp Intellectual Disability panel, and all discrepancies have been resolved, with reciprocal reviews provided to Genomics England, 11/3/2020.",
                "status": "public",
                "version": "1.760",
                "version_created": "2026-04-26T17:50:23.271073+10:00",
                "relevant_disorders": [
                    "Intellectual disability",
                    "HP:0001249; Neurodevelopmental delay",
                    "HP:0012758"
                ],
                "stats": {
                    "number_of_genes": 2524,
                    "number_of_strs": 10,
                    "number_of_regions": 57
                },
                "types": [
                    {
                        "name": "Genetic Health Queensland",
                        "slug": "genetic-health-queensland",
                        "description": "Panel used by GHQ."
                    },
                    {
                        "name": "Victorian Clinical Genetics Services",
                        "slug": "victorian-clinical-genetics-services",
                        "description": "Panel used by VCGS."
                    },
                    {
                        "name": "Rare Disease",
                        "slug": "rare-disease",
                        "description": "Rare disease panels"
                    },
                    {
                        "name": "Royal Melbourne Hospital",
                        "slug": "royal-melbourne-hospital",
                        "description": "Royal Melbourne Hospital"
                    }
                ],
                "child_panel_ids": []
            },
            "transcript": null
        },
        {
            "gene_data": {
                "alias": [
                    "MRL3"
                ],
                "biotype": "protein_coding",
                "hgnc_id": "HGNC:10379",
                "gene_name": "mitochondrial ribosomal protein L3",
                "omim_gene": [
                    "607118"
                ],
                "alias_name": null,
                "gene_symbol": "MRPL3",
                "hgnc_symbol": "MRPL3",
                "hgnc_release": "2017-11-03",
                "ensembl_genes": {
                    "GRch37": {
                        "82": {
                            "location": "3:131181056-131221827",
                            "ensembl_id": "ENSG00000114686"
                        }
                    },
                    "GRch38": {
                        "90": {
                            "location": "3:131462212-131502983",
                            "ensembl_id": "ENSG00000114686"
                        }
                    }
                },
                "hgnc_date_symbol_changed": "1999-09-16"
            },
            "entity_type": "gene",
            "entity_name": "MRPL3",
            "confidence_level": "2",
            "penetrance": null,
            "mode_of_pathogenicity": "",
            "publications": [
                "PubMed: 27815843",
                "21786366"
            ],
            "evidence": [
                "Expert Review Amber",
                "Expert list"
            ],
            "phenotypes": [
                "Combined oxidative phosphorylation deficiency 9",
                "OMIM #614582"
            ],
            "mode_of_inheritance": "BIALLELIC, autosomal or pseudoautosomal",
            "tags": [],
            "panel": {
                "id": 250,
                "hash_id": null,
                "name": "Intellectual disability syndromic and non-syndromic",
                "disease_group": "Neurology and neurodevelopmental disorders",
                "disease_sub_group": "",
                "description": "This panel was created by merging the ID panels used by Genetic Health Queensland and by the Victorian Clinical Genetics Services. Discrepant gene classifications reviewed and resolved by Chirag Patel and Zornitza Stark.\r\n\r\nThis is a consensus panel used by VCGS, GHQ and RMH.\r\n\r\nThis panel has been compared against the Genomics England PanelApp Intellectual Disability panel, and all discrepancies have been resolved, with reciprocal reviews provided to Genomics England, 11/3/2020.",
                "status": "public",
                "version": "1.760",
                "version_created": "2026-04-26T17:50:23.271073+10:00",
                "relevant_disorders": [
                    "Intellectual disability",
                    "HP:0001249; Neurodevelopmental delay",
                    "HP:0012758"
                ],
                "stats": {
                    "number_of_genes": 2524,
                    "number_of_strs": 10,
                    "number_of_regions": 57
                },
                "types": [
                    {
                        "name": "Genetic Health Queensland",
                        "slug": "genetic-health-queensland",
                        "description": "Panel used by GHQ."
                    },
                    {
                        "name": "Victorian Clinical Genetics Services",
                        "slug": "victorian-clinical-genetics-services",
                        "description": "Panel used by VCGS."
                    },
                    {
                        "name": "Rare Disease",
                        "slug": "rare-disease",
                        "description": "Rare disease panels"
                    },
                    {
                        "name": "Royal Melbourne Hospital",
                        "slug": "royal-melbourne-hospital",
                        "description": "Royal Melbourne Hospital"
                    }
                ],
                "child_panel_ids": []
            },
            "transcript": null
        },
        {
            "gene_data": {
                "alias": [
                    "CGI-132"
                ],
                "biotype": "protein_coding",
                "hgnc_id": "HGNC:14048",
                "gene_name": "mitochondrial ribosomal protein S16",
                "omim_gene": [
                    "609204"
                ],
                "alias_name": null,
                "gene_symbol": "MRPS16",
                "hgnc_symbol": "MRPS16",
                "hgnc_release": "2017-11-03",
                "ensembl_genes": {
                    "GRch37": {
                        "82": {
                            "location": "10:75006510-75012451",
                            "ensembl_id": "ENSG00000182180"
                        }
                    },
                    "GRch38": {
                        "90": {
                            "location": "10:73248843-73252693",
                            "ensembl_id": "ENSG00000182180"
                        }
                    }
                },
                "hgnc_date_symbol_changed": "2001-02-28"
            },
            "entity_type": "gene",
            "entity_name": "MRPS16",
            "confidence_level": "1",
            "penetrance": null,
            "mode_of_pathogenicity": "",
            "publications": [
                "PubMed: 15505824"
            ],
            "evidence": [
                "Expert Review Red",
                "Expert list"
            ],
            "phenotypes": [
                "Combined oxidative phosphorylation deficiency 2",
                "OMIM #610498"
            ],
            "mode_of_inheritance": "BIALLELIC, autosomal or pseudoautosomal",
            "tags": [],
            "panel": {
                "id": 250,
                "hash_id": null,
                "name": "Intellectual disability syndromic and non-syndromic",
                "disease_group": "Neurology and neurodevelopmental disorders",
                "disease_sub_group": "",
                "description": "This panel was created by merging the ID panels used by Genetic Health Queensland and by the Victorian Clinical Genetics Services. Discrepant gene classifications reviewed and resolved by Chirag Patel and Zornitza Stark.\r\n\r\nThis is a consensus panel used by VCGS, GHQ and RMH.\r\n\r\nThis panel has been compared against the Genomics England PanelApp Intellectual Disability panel, and all discrepancies have been resolved, with reciprocal reviews provided to Genomics England, 11/3/2020.",
                "status": "public",
                "version": "1.760",
                "version_created": "2026-04-26T17:50:23.271073+10:00",
                "relevant_disorders": [
                    "Intellectual disability",
                    "HP:0001249; Neurodevelopmental delay",
                    "HP:0012758"
                ],
                "stats": {
                    "number_of_genes": 2524,
                    "number_of_strs": 10,
                    "number_of_regions": 57
                },
                "types": [
                    {
                        "name": "Genetic Health Queensland",
                        "slug": "genetic-health-queensland",
                        "description": "Panel used by GHQ."
                    },
                    {
                        "name": "Victorian Clinical Genetics Services",
                        "slug": "victorian-clinical-genetics-services",
                        "description": "Panel used by VCGS."
                    },
                    {
                        "name": "Rare Disease",
                        "slug": "rare-disease",
                        "description": "Rare disease panels"
                    },
                    {
                        "name": "Royal Melbourne Hospital",
                        "slug": "royal-melbourne-hospital",
                        "description": "Royal Melbourne Hospital"
                    }
                ],
                "child_panel_ids": []
            },
            "transcript": null
        },
        {
            "gene_data": {
                "alias": [
                    "MRP-S22",
                    "GK002",
                    "C3orf5",
                    "GIBT"
                ],
                "biotype": "protein_coding",
                "hgnc_id": "HGNC:14508",
                "gene_name": "mitochondrial ribosomal protein S22",
                "omim_gene": [
                    "605810"
                ],
                "alias_name": null,
                "gene_symbol": "MRPS22",
                "hgnc_symbol": "MRPS22",
                "hgnc_release": "2017-11-03",
                "ensembl_genes": {
                    "GRch37": {
                        "82": {
                            "location": "3:138724648-139076065",
                            "ensembl_id": "ENSG00000175110"
                        }
                    },
                    "GRch38": {
                        "90": {
                            "location": "3:139005806-139357223",
                            "ensembl_id": "ENSG00000175110"
                        }
                    }
                },
                "hgnc_date_symbol_changed": "2001-01-26"
            },
            "entity_type": "gene",
            "entity_name": "MRPS22",
            "confidence_level": "3",
            "penetrance": null,
            "mode_of_pathogenicity": "",
            "publications": [
                "29566152",
                "17873122",
                "25663021",
                "28752220"
            ],
            "evidence": [
                "Expert Review Green",
                "Genetic Health Queensland"
            ],
            "phenotypes": [
                "Combined oxidative phosphorylation deficiency 5 MIM#611719"
            ],
            "mode_of_inheritance": "BIALLELIC, autosomal or pseudoautosomal",
            "tags": [],
            "panel": {
                "id": 250,
                "hash_id": null,
                "name": "Intellectual disability syndromic and non-syndromic",
                "disease_group": "Neurology and neurodevelopmental disorders",
                "disease_sub_group": "",
                "description": "This panel was created by merging the ID panels used by Genetic Health Queensland and by the Victorian Clinical Genetics Services. Discrepant gene classifications reviewed and resolved by Chirag Patel and Zornitza Stark.\r\n\r\nThis is a consensus panel used by VCGS, GHQ and RMH.\r\n\r\nThis panel has been compared against the Genomics England PanelApp Intellectual Disability panel, and all discrepancies have been resolved, with reciprocal reviews provided to Genomics England, 11/3/2020.",
                "status": "public",
                "version": "1.760",
                "version_created": "2026-04-26T17:50:23.271073+10:00",
                "relevant_disorders": [
                    "Intellectual disability",
                    "HP:0001249; Neurodevelopmental delay",
                    "HP:0012758"
                ],
                "stats": {
                    "number_of_genes": 2524,
                    "number_of_strs": 10,
                    "number_of_regions": 57
                },
                "types": [
                    {
                        "name": "Genetic Health Queensland",
                        "slug": "genetic-health-queensland",
                        "description": "Panel used by GHQ."
                    },
                    {
                        "name": "Victorian Clinical Genetics Services",
                        "slug": "victorian-clinical-genetics-services",
                        "description": "Panel used by VCGS."
                    },
                    {
                        "name": "Rare Disease",
                        "slug": "rare-disease",
                        "description": "Rare disease panels"
                    },
                    {
                        "name": "Royal Melbourne Hospital",
                        "slug": "royal-melbourne-hospital",
                        "description": "Royal Melbourne Hospital"
                    }
                ],
                "child_panel_ids": []
            },
            "transcript": null
        },
        {
            "gene_data": {
                "alias": [],
                "biotype": "protein_coding",
                "hgnc_id": "HGNC:7329",
                "gene_name": "mutS homolog 6",
                "omim_gene": [
                    "600678"
                ],
                "alias_name": null,
                "gene_symbol": "MSH6",
                "hgnc_symbol": "MSH6",
                "hgnc_release": "2017-11-03",
                "ensembl_genes": {
                    "GRch37": {
                        "82": {
                            "location": "2:47922669-48037240",
                            "ensembl_id": "ENSG00000116062"
                        }
                    },
                    "GRch38": {
                        "90": {
                            "location": "2:47695530-47810101",
                            "ensembl_id": "ENSG00000116062"
                        }
                    }
                },
                "hgnc_date_symbol_changed": "1995-08-29"
            },
            "entity_type": "gene",
            "entity_name": "MSH6",
            "confidence_level": "1",
            "penetrance": null,
            "mode_of_pathogenicity": "",
            "publications": [],
            "evidence": [
                "Expert Review Red",
                "Expert list"
            ],
            "phenotypes": [
                "Colorectal cancer, hereditary nonpolyposis, type 5, OMIM #614350",
                "Mismatch repair cancer syndrome, OMIM #276300"
            ],
            "mode_of_inheritance": "BOTH monoallelic and biallelic, autosomal or pseudoautosomal",
            "tags": [],
            "panel": {
                "id": 250,
                "hash_id": null,
                "name": "Intellectual disability syndromic and non-syndromic",
                "disease_group": "Neurology and neurodevelopmental disorders",
                "disease_sub_group": "",
                "description": "This panel was created by merging the ID panels used by Genetic Health Queensland and by the Victorian Clinical Genetics Services. Discrepant gene classifications reviewed and resolved by Chirag Patel and Zornitza Stark.\r\n\r\nThis is a consensus panel used by VCGS, GHQ and RMH.\r\n\r\nThis panel has been compared against the Genomics England PanelApp Intellectual Disability panel, and all discrepancies have been resolved, with reciprocal reviews provided to Genomics England, 11/3/2020.",
                "status": "public",
                "version": "1.760",
                "version_created": "2026-04-26T17:50:23.271073+10:00",
                "relevant_disorders": [
                    "Intellectual disability",
                    "HP:0001249; Neurodevelopmental delay",
                    "HP:0012758"
                ],
                "stats": {
                    "number_of_genes": 2524,
                    "number_of_strs": 10,
                    "number_of_regions": 57
                },
                "types": [
                    {
                        "name": "Genetic Health Queensland",
                        "slug": "genetic-health-queensland",
                        "description": "Panel used by GHQ."
                    },
                    {
                        "name": "Victorian Clinical Genetics Services",
                        "slug": "victorian-clinical-genetics-services",
                        "description": "Panel used by VCGS."
                    },
                    {
                        "name": "Rare Disease",
                        "slug": "rare-disease",
                        "description": "Rare disease panels"
                    },
                    {
                        "name": "Royal Melbourne Hospital",
                        "slug": "royal-melbourne-hospital",
                        "description": "Royal Melbourne Hospital"
                    }
                ],
                "child_panel_ids": []
            },
            "transcript": null
        },
        {
            "gene_data": {
                "alias": [
                    "FMT1"
                ],
                "biotype": "protein_coding",
                "hgnc_id": "HGNC:29666",
                "gene_name": "mitochondrial methionyl-tRNA formyltransferase",
                "omim_gene": [
                    "611766"
                ],
                "alias_name": null,
                "gene_symbol": "MTFMT",
                "hgnc_symbol": "MTFMT",
                "hgnc_release": "2017-11-03",
                "ensembl_genes": {
                    "GRch37": {
                        "82": {
                            "location": "15:65294845-65321977",
                            "ensembl_id": "ENSG00000103707"
                        }
                    },
                    "GRch38": {
                        "90": {
                            "location": "15:65001512-65029639",
                            "ensembl_id": "ENSG00000103707"
                        }
                    }
                },
                "hgnc_date_symbol_changed": "2005-08-09"
            },
            "entity_type": "gene",
            "entity_name": "MTFMT",
            "confidence_level": "3",
            "penetrance": null,
            "mode_of_pathogenicity": "",
            "publications": [
                "21907147",
                "23499752",
                "24461907",
                "22499348"
            ],
            "evidence": [
                "Expert Review Green",
                "Genetic Health Queensland"
            ],
            "phenotypes": [
                "Combined oxidative phosphorylation deficiency 15, MIM# 614947",
                "Mitochondrial complex I deficiency, nuclear type 27, MIM# 618248"
            ],
            "mode_of_inheritance": "BIALLELIC, autosomal or pseudoautosomal",
            "tags": [],
            "panel": {
                "id": 250,
                "hash_id": null,
                "name": "Intellectual disability syndromic and non-syndromic",
                "disease_group": "Neurology and neurodevelopmental disorders",
                "disease_sub_group": "",
                "description": "This panel was created by merging the ID panels used by Genetic Health Queensland and by the Victorian Clinical Genetics Services. Discrepant gene classifications reviewed and resolved by Chirag Patel and Zornitza Stark.\r\n\r\nThis is a consensus panel used by VCGS, GHQ and RMH.\r\n\r\nThis panel has been compared against the Genomics England PanelApp Intellectual Disability panel, and all discrepancies have been resolved, with reciprocal reviews provided to Genomics England, 11/3/2020.",
                "status": "public",
                "version": "1.760",
                "version_created": "2026-04-26T17:50:23.271073+10:00",
                "relevant_disorders": [
                    "Intellectual disability",
                    "HP:0001249; Neurodevelopmental delay",
                    "HP:0012758"
                ],
                "stats": {
                    "number_of_genes": 2524,
                    "number_of_strs": 10,
                    "number_of_regions": 57
                },
                "types": [
                    {
                        "name": "Genetic Health Queensland",
                        "slug": "genetic-health-queensland",
                        "description": "Panel used by GHQ."
                    },
                    {
                        "name": "Victorian Clinical Genetics Services",
                        "slug": "victorian-clinical-genetics-services",
                        "description": "Panel used by VCGS."
                    },
                    {
                        "name": "Rare Disease",
                        "slug": "rare-disease",
                        "description": "Rare disease panels"
                    },
                    {
                        "name": "Royal Melbourne Hospital",
                        "slug": "royal-melbourne-hospital",
                        "description": "Royal Melbourne Hospital"
                    }
                ],
                "child_panel_ids": []
            },
            "transcript": null
        },
        {
            "gene_data": {
                "alias": [],
                "biotype": "protein_coding",
                "hgnc_id": "HGNC:7436",
                "gene_name": "methylenetetrahydrofolate reductase",
                "omim_gene": [
                    "607093"
                ],
                "alias_name": null,
                "gene_symbol": "MTHFR",
                "hgnc_symbol": "MTHFR",
                "hgnc_release": "2017-11-03",
                "ensembl_genes": {
                    "GRch37": {
                        "82": {
                            "location": "1:11845780-11866977",
                            "ensembl_id": "ENSG00000177000"
                        }
                    },
                    "GRch38": {
                        "90": {
                            "location": "1:11785723-11806920",
                            "ensembl_id": "ENSG00000177000"
                        }
                    }
                },
                "hgnc_date_symbol_changed": "1994-07-15"
            },
            "entity_type": "gene",
            "entity_name": "MTHFR",
            "confidence_level": "3",
            "penetrance": null,
            "mode_of_pathogenicity": "",
            "publications": [
                "27604308",
                "7920641"
            ],
            "evidence": [
                "Expert Review Green",
                "Genetic Health Queensland"
            ],
            "phenotypes": [
                "Homocystinuria due to MTHFR deficiency MIM#236250",
                "Disorders of folate metabolism and transport"
            ],
            "mode_of_inheritance": "BIALLELIC, autosomal or pseudoautosomal",
            "tags": [],
            "panel": {
                "id": 250,
                "hash_id": null,
                "name": "Intellectual disability syndromic and non-syndromic",
                "disease_group": "Neurology and neurodevelopmental disorders",
                "disease_sub_group": "",
                "description": "This panel was created by merging the ID panels used by Genetic Health Queensland and by the Victorian Clinical Genetics Services. Discrepant gene classifications reviewed and resolved by Chirag Patel and Zornitza Stark.\r\n\r\nThis is a consensus panel used by VCGS, GHQ and RMH.\r\n\r\nThis panel has been compared against the Genomics England PanelApp Intellectual Disability panel, and all discrepancies have been resolved, with reciprocal reviews provided to Genomics England, 11/3/2020.",
                "status": "public",
                "version": "1.760",
                "version_created": "2026-04-26T17:50:23.271073+10:00",
                "relevant_disorders": [
                    "Intellectual disability",
                    "HP:0001249; Neurodevelopmental delay",
                    "HP:0012758"
                ],
                "stats": {
                    "number_of_genes": 2524,
                    "number_of_strs": 10,
                    "number_of_regions": 57
                },
                "types": [
                    {
                        "name": "Genetic Health Queensland",
                        "slug": "genetic-health-queensland",
                        "description": "Panel used by GHQ."
                    },
                    {
                        "name": "Victorian Clinical Genetics Services",
                        "slug": "victorian-clinical-genetics-services",
                        "description": "Panel used by VCGS."
                    },
                    {
                        "name": "Rare Disease",
                        "slug": "rare-disease",
                        "description": "Rare disease panels"
                    },
                    {
                        "name": "Royal Melbourne Hospital",
                        "slug": "royal-melbourne-hospital",
                        "description": "Royal Melbourne Hospital"
                    }
                ],
                "child_panel_ids": []
            },
            "transcript": null
        },
        {
            "gene_data": {
                "alias": [],
                "biotype": "protein_coding",
                "hgnc_id": "HGNC:7448",
                "gene_name": "myotubularin 1",
                "omim_gene": [
                    "300415"
                ],
                "alias_name": null,
                "gene_symbol": "MTM1",
                "hgnc_symbol": "MTM1",
                "hgnc_release": "2017-11-03",
                "ensembl_genes": {
                    "GRch37": {
                        "82": {
                            "location": "X:149737069-149841795",
                            "ensembl_id": "ENSG00000171100"
                        }
                    },
                    "GRch38": {
                        "90": {
                            "location": "X:150568619-150673322",
                            "ensembl_id": "ENSG00000171100"
                        }
                    }
                },
                "hgnc_date_symbol_changed": "2001-06-22"
            },
            "entity_type": "gene",
            "entity_name": "MTM1",
            "confidence_level": "1",
            "penetrance": null,
            "mode_of_pathogenicity": "",
            "publications": [],
            "evidence": [
                "Expert Review Red",
                "Expert list"
            ],
            "phenotypes": [
                "Myotubular myopathy, X-linked",
                "OMIM#310400"
            ],
            "mode_of_inheritance": "X-LINKED: hemizygous mutation in males, biallelic mutations in females",
            "tags": [],
            "panel": {
                "id": 250,
                "hash_id": null,
                "name": "Intellectual disability syndromic and non-syndromic",
                "disease_group": "Neurology and neurodevelopmental disorders",
                "disease_sub_group": "",
                "description": "This panel was created by merging the ID panels used by Genetic Health Queensland and by the Victorian Clinical Genetics Services. Discrepant gene classifications reviewed and resolved by Chirag Patel and Zornitza Stark.\r\n\r\nThis is a consensus panel used by VCGS, GHQ and RMH.\r\n\r\nThis panel has been compared against the Genomics England PanelApp Intellectual Disability panel, and all discrepancies have been resolved, with reciprocal reviews provided to Genomics England, 11/3/2020.",
                "status": "public",
                "version": "1.760",
                "version_created": "2026-04-26T17:50:23.271073+10:00",
                "relevant_disorders": [
                    "Intellectual disability",
                    "HP:0001249; Neurodevelopmental delay",
                    "HP:0012758"
                ],
                "stats": {
                    "number_of_genes": 2524,
                    "number_of_strs": 10,
                    "number_of_regions": 57
                },
                "types": [
                    {
                        "name": "Genetic Health Queensland",
                        "slug": "genetic-health-queensland",
                        "description": "Panel used by GHQ."
                    },
                    {
                        "name": "Victorian Clinical Genetics Services",
                        "slug": "victorian-clinical-genetics-services",
                        "description": "Panel used by VCGS."
                    },
                    {
                        "name": "Rare Disease",
                        "slug": "rare-disease",
                        "description": "Rare disease panels"
                    },
                    {
                        "name": "Royal Melbourne Hospital",
                        "slug": "royal-melbourne-hospital",
                        "description": "Royal Melbourne Hospital"
                    }
                ],
                "child_panel_ids": []
            },
            "transcript": null
        },
        {
            "gene_data": {
                "alias": [
                    "KIAA1073"
                ],
                "biotype": "protein_coding",
                "hgnc_id": "HGNC:7450",
                "gene_name": "myotubularin related protein 2",
                "omim_gene": [
                    "603557"
                ],
                "alias_name": [
                    "phosphatidylinositol-3-phosphatase",
                    "phosphoinositide-3-phosphatase"
                ],
                "gene_symbol": "MTMR2",
                "hgnc_symbol": "MTMR2",
                "hgnc_release": "2017-11-03",
                "ensembl_genes": {
                    "GRch37": {
                        "82": {
                            "location": "11:95566046-95658479",
                            "ensembl_id": "ENSG00000087053"
                        }
                    },
                    "GRch38": {
                        "90": {
                            "location": "11:95832882-95925315",
                            "ensembl_id": "ENSG00000087053"
                        }
                    }
                },
                "hgnc_date_symbol_changed": "1999-02-05"
            },
            "entity_type": "gene",
            "entity_name": "MTMR2",
            "confidence_level": "1",
            "penetrance": null,
            "mode_of_pathogenicity": "",
            "publications": [],
            "evidence": [
                "Expert Review Red",
                "Expert list"
            ],
            "phenotypes": [
                "Charcot-Marie-Tooth disease, type 4B1",
                "OMIM #601382"
            ],
            "mode_of_inheritance": "BIALLELIC, autosomal or pseudoautosomal",
            "tags": [],
            "panel": {
                "id": 250,
                "hash_id": null,
                "name": "Intellectual disability syndromic and non-syndromic",
                "disease_group": "Neurology and neurodevelopmental disorders",
                "disease_sub_group": "",
                "description": "This panel was created by merging the ID panels used by Genetic Health Queensland and by the Victorian Clinical Genetics Services. Discrepant gene classifications reviewed and resolved by Chirag Patel and Zornitza Stark.\r\n\r\nThis is a consensus panel used by VCGS, GHQ and RMH.\r\n\r\nThis panel has been compared against the Genomics England PanelApp Intellectual Disability panel, and all discrepancies have been resolved, with reciprocal reviews provided to Genomics England, 11/3/2020.",
                "status": "public",
                "version": "1.760",
                "version_created": "2026-04-26T17:50:23.271073+10:00",
                "relevant_disorders": [
                    "Intellectual disability",
                    "HP:0001249; Neurodevelopmental delay",
                    "HP:0012758"
                ],
                "stats": {
                    "number_of_genes": 2524,
                    "number_of_strs": 10,
                    "number_of_regions": 57
                },
                "types": [
                    {
                        "name": "Genetic Health Queensland",
                        "slug": "genetic-health-queensland",
                        "description": "Panel used by GHQ."
                    },
                    {
                        "name": "Victorian Clinical Genetics Services",
                        "slug": "victorian-clinical-genetics-services",
                        "description": "Panel used by VCGS."
                    },
                    {
                        "name": "Rare Disease",
                        "slug": "rare-disease",
                        "description": "Rare disease panels"
                    },
                    {
                        "name": "Royal Melbourne Hospital",
                        "slug": "royal-melbourne-hospital",
                        "description": "Royal Melbourne Hospital"
                    }
                ],
                "child_panel_ids": []
            },
            "transcript": null
        },
        {
            "gene_data": {
                "alias": [],
                "biotype": "protein_coding",
                "hgnc_id": "HGNC:19261",
                "gene_name": "mitochondrial tRNA translation optimization 1",
                "omim_gene": [
                    "614667"
                ],
                "alias_name": null,
                "gene_symbol": "MTO1",
                "hgnc_symbol": "MTO1",
                "hgnc_release": "2017-11-03",
                "ensembl_genes": {
                    "GRch37": {
                        "82": {
                            "location": "6:74171301-74218959",
                            "ensembl_id": "ENSG00000135297"
                        }
                    },
                    "GRch38": {
                        "90": {
                            "location": "6:73461578-73509236",
                            "ensembl_id": "ENSG00000135297"
                        }
                    }
                },
                "hgnc_date_symbol_changed": "2003-05-21"
            },
            "entity_type": "gene",
            "entity_name": "MTO1",
            "confidence_level": "3",
            "penetrance": null,
            "mode_of_pathogenicity": "",
            "publications": [
                "PMID: 26061759",
                "29331171",
                "23929671"
            ],
            "evidence": [
                "Expert Review Green",
                "Expert list"
            ],
            "phenotypes": [
                "Combined oxidative phosphorylation deficiency 10",
                "OMIM #614702"
            ],
            "mode_of_inheritance": "BIALLELIC, autosomal or pseudoautosomal",
            "tags": [],
            "panel": {
                "id": 250,
                "hash_id": null,
                "name": "Intellectual disability syndromic and non-syndromic",
                "disease_group": "Neurology and neurodevelopmental disorders",
                "disease_sub_group": "",
                "description": "This panel was created by merging the ID panels used by Genetic Health Queensland and by the Victorian Clinical Genetics Services. Discrepant gene classifications reviewed and resolved by Chirag Patel and Zornitza Stark.\r\n\r\nThis is a consensus panel used by VCGS, GHQ and RMH.\r\n\r\nThis panel has been compared against the Genomics England PanelApp Intellectual Disability panel, and all discrepancies have been resolved, with reciprocal reviews provided to Genomics England, 11/3/2020.",
                "status": "public",
                "version": "1.760",
                "version_created": "2026-04-26T17:50:23.271073+10:00",
                "relevant_disorders": [
                    "Intellectual disability",
                    "HP:0001249; Neurodevelopmental delay",
                    "HP:0012758"
                ],
                "stats": {
                    "number_of_genes": 2524,
                    "number_of_strs": 10,
                    "number_of_regions": 57
                },
                "types": [
                    {
                        "name": "Genetic Health Queensland",
                        "slug": "genetic-health-queensland",
                        "description": "Panel used by GHQ."
                    },
                    {
                        "name": "Victorian Clinical Genetics Services",
                        "slug": "victorian-clinical-genetics-services",
                        "description": "Panel used by VCGS."
                    },
                    {
                        "name": "Rare Disease",
                        "slug": "rare-disease",
                        "description": "Rare disease panels"
                    },
                    {
                        "name": "Royal Melbourne Hospital",
                        "slug": "royal-melbourne-hospital",
                        "description": "Royal Melbourne Hospital"
                    }
                ],
                "child_panel_ids": []
            },
            "transcript": null
        },
        {
            "gene_data": {
                "alias": [
                    "FLJ10486",
                    "mtPAP",
                    "SPAX4"
                ],
                "biotype": "protein_coding",
                "hgnc_id": "HGNC:25532",
                "gene_name": "mitochondrial poly(A) polymerase",
                "omim_gene": [
                    "613669"
                ],
                "alias_name": [
                    "TUTase1"
                ],
                "gene_symbol": "MTPAP",
                "hgnc_symbol": "MTPAP",
                "hgnc_release": "2017-11-03",
                "ensembl_genes": {
                    "GRch37": {
                        "82": {
                            "location": "10:30598730-30663377",
                            "ensembl_id": "ENSG00000107951"
                        }
                    },
                    "GRch38": {
                        "90": {
                            "location": "10:30309801-30374448",
                            "ensembl_id": "ENSG00000107951"
                        }
                    }
                },
                "hgnc_date_symbol_changed": "2009-01-12"
            },
            "entity_type": "gene",
            "entity_name": "MTPAP",
            "confidence_level": "1",
            "penetrance": null,
            "mode_of_pathogenicity": "",
            "publications": [],
            "evidence": [
                "Expert Review Red",
                "Expert list"
            ],
            "phenotypes": [
                "?Spastic ataxia 4, autosomal recessive",
                "OMIM#613672"
            ],
            "mode_of_inheritance": "BIALLELIC, autosomal or pseudoautosomal",
            "tags": [],
            "panel": {
                "id": 250,
                "hash_id": null,
                "name": "Intellectual disability syndromic and non-syndromic",
                "disease_group": "Neurology and neurodevelopmental disorders",
                "disease_sub_group": "",
                "description": "This panel was created by merging the ID panels used by Genetic Health Queensland and by the Victorian Clinical Genetics Services. Discrepant gene classifications reviewed and resolved by Chirag Patel and Zornitza Stark.\r\n\r\nThis is a consensus panel used by VCGS, GHQ and RMH.\r\n\r\nThis panel has been compared against the Genomics England PanelApp Intellectual Disability panel, and all discrepancies have been resolved, with reciprocal reviews provided to Genomics England, 11/3/2020.",
                "status": "public",
                "version": "1.760",
                "version_created": "2026-04-26T17:50:23.271073+10:00",
                "relevant_disorders": [
                    "Intellectual disability",
                    "HP:0001249; Neurodevelopmental delay",
                    "HP:0012758"
                ],
                "stats": {
                    "number_of_genes": 2524,
                    "number_of_strs": 10,
                    "number_of_regions": 57
                },
                "types": [
                    {
                        "name": "Genetic Health Queensland",
                        "slug": "genetic-health-queensland",
                        "description": "Panel used by GHQ."
                    },
                    {
                        "name": "Victorian Clinical Genetics Services",
                        "slug": "victorian-clinical-genetics-services",
                        "description": "Panel used by VCGS."
                    },
                    {
                        "name": "Rare Disease",
                        "slug": "rare-disease",
                        "description": "Rare disease panels"
                    },
                    {
                        "name": "Royal Melbourne Hospital",
                        "slug": "royal-melbourne-hospital",
                        "description": "Royal Melbourne Hospital"
                    }
                ],
                "child_panel_ids": []
            },
            "transcript": null
        },
        {
            "gene_data": {
                "alias": [
                    "cblG"
                ],
                "biotype": "protein_coding",
                "hgnc_id": "HGNC:7468",
                "gene_name": "5-methyltetrahydrofolate-homocysteine methyltransferase",
                "omim_gene": [
                    "156570"
                ],
                "alias_name": null,
                "gene_symbol": "MTR",
                "hgnc_symbol": "MTR",
                "hgnc_release": "2017-11-03",
                "ensembl_genes": {
                    "GRch37": {
                        "82": {
                            "location": "1:236958610-237067281",
                            "ensembl_id": "ENSG00000116984"
                        }
                    },
                    "GRch38": {
                        "90": {
                            "location": "1:236795281-236903981",
                            "ensembl_id": "ENSG00000116984"
                        }
                    }
                },
                "hgnc_date_symbol_changed": "1986-01-01"
            },
            "entity_type": "gene",
            "entity_name": "MTR",
            "confidence_level": "3",
            "penetrance": null,
            "mode_of_pathogenicity": "",
            "publications": [
                "8968736",
                "8968737",
                "9683607",
                "12068375"
            ],
            "evidence": [
                "Expert Review Green",
                "Genetic Health Queensland"
            ],
            "phenotypes": [
                "Homocystinuria-megaloblastic anaemia, cblG complementation type, MIM# 250940"
            ],
            "mode_of_inheritance": "BIALLELIC, autosomal or pseudoautosomal",
            "tags": [],
            "panel": {
                "id": 250,
                "hash_id": null,
                "name": "Intellectual disability syndromic and non-syndromic",
                "disease_group": "Neurology and neurodevelopmental disorders",
                "disease_sub_group": "",
                "description": "This panel was created by merging the ID panels used by Genetic Health Queensland and by the Victorian Clinical Genetics Services. Discrepant gene classifications reviewed and resolved by Chirag Patel and Zornitza Stark.\r\n\r\nThis is a consensus panel used by VCGS, GHQ and RMH.\r\n\r\nThis panel has been compared against the Genomics England PanelApp Intellectual Disability panel, and all discrepancies have been resolved, with reciprocal reviews provided to Genomics England, 11/3/2020.",
                "status": "public",
                "version": "1.760",
                "version_created": "2026-04-26T17:50:23.271073+10:00",
                "relevant_disorders": [
                    "Intellectual disability",
                    "HP:0001249; Neurodevelopmental delay",
                    "HP:0012758"
                ],
                "stats": {
                    "number_of_genes": 2524,
                    "number_of_strs": 10,
                    "number_of_regions": 57
                },
                "types": [
                    {
                        "name": "Genetic Health Queensland",
                        "slug": "genetic-health-queensland",
                        "description": "Panel used by GHQ."
                    },
                    {
                        "name": "Victorian Clinical Genetics Services",
                        "slug": "victorian-clinical-genetics-services",
                        "description": "Panel used by VCGS."
                    },
                    {
                        "name": "Rare Disease",
                        "slug": "rare-disease",
                        "description": "Rare disease panels"
                    },
                    {
                        "name": "Royal Melbourne Hospital",
                        "slug": "royal-melbourne-hospital",
                        "description": "Royal Melbourne Hospital"
                    }
                ],
                "child_panel_ids": []
            },
            "transcript": null
        },
        {
            "gene_data": {
                "alias": [
                    "cblE"
                ],
                "biotype": "protein_coding",
                "hgnc_id": "HGNC:7473",
                "gene_name": "5-methyltetrahydrofolate-homocysteine methyltransferase reductase",
                "omim_gene": [
                    "602568"
                ],
                "alias_name": null,
                "gene_symbol": "MTRR",
                "hgnc_symbol": "MTRR",
                "hgnc_release": "2017-11-03",
                "ensembl_genes": {
                    "GRch37": {
                        "82": {
                            "location": "5:7851299-7906138",
                            "ensembl_id": "ENSG00000124275"
                        }
                    },
                    "GRch38": {
                        "90": {
                            "location": "5:7851186-7906025",
                            "ensembl_id": "ENSG00000124275"
                        }
                    }
                },
                "hgnc_date_symbol_changed": "1998-04-20"
            },
            "entity_type": "gene",
            "entity_name": "MTRR",
            "confidence_level": "3",
            "penetrance": null,
            "mode_of_pathogenicity": "",
            "publications": [
                "12555939",
                "15714522"
            ],
            "evidence": [
                "Expert Review Green",
                "Genetic Health Queensland"
            ],
            "phenotypes": [
                "Homocystinuria-megaloblastic anaemia, cbl E type, MIM# 236270"
            ],
            "mode_of_inheritance": "BIALLELIC, autosomal or pseudoautosomal",
            "tags": [],
            "panel": {
                "id": 250,
                "hash_id": null,
                "name": "Intellectual disability syndromic and non-syndromic",
                "disease_group": "Neurology and neurodevelopmental disorders",
                "disease_sub_group": "",
                "description": "This panel was created by merging the ID panels used by Genetic Health Queensland and by the Victorian Clinical Genetics Services. Discrepant gene classifications reviewed and resolved by Chirag Patel and Zornitza Stark.\r\n\r\nThis is a consensus panel used by VCGS, GHQ and RMH.\r\n\r\nThis panel has been compared against the Genomics England PanelApp Intellectual Disability panel, and all discrepancies have been resolved, with reciprocal reviews provided to Genomics England, 11/3/2020.",
                "status": "public",
                "version": "1.760",
                "version_created": "2026-04-26T17:50:23.271073+10:00",
                "relevant_disorders": [
                    "Intellectual disability",
                    "HP:0001249; Neurodevelopmental delay",
                    "HP:0012758"
                ],
                "stats": {
                    "number_of_genes": 2524,
                    "number_of_strs": 10,
                    "number_of_regions": 57
                },
                "types": [
                    {
                        "name": "Genetic Health Queensland",
                        "slug": "genetic-health-queensland",
                        "description": "Panel used by GHQ."
                    },
                    {
                        "name": "Victorian Clinical Genetics Services",
                        "slug": "victorian-clinical-genetics-services",
                        "description": "Panel used by VCGS."
                    },
                    {
                        "name": "Rare Disease",
                        "slug": "rare-disease",
                        "description": "Rare disease panels"
                    },
                    {
                        "name": "Royal Melbourne Hospital",
                        "slug": "royal-melbourne-hospital",
                        "description": "Royal Melbourne Hospital"
                    }
                ],
                "child_panel_ids": []
            },
            "transcript": null
        },
        {
            "gene_data": {
                "alias": [],
                "biotype": "protein_coding",
                "hgnc_id": "HGNC:7526",
                "gene_name": "methylmalonyl-CoA mutase",
                "omim_gene": [
                    "609058"
                ],
                "alias_name": null,
                "gene_symbol": "MUT",
                "hgnc_symbol": "MUT",
                "hgnc_release": "2017-11-03",
                "ensembl_genes": {
                    "GRch37": {
                        "82": {
                            "location": "6:49398073-49430904",
                            "ensembl_id": "ENSG00000146085"
                        }
                    },
                    "GRch38": {
                        "90": {
                            "location": "6:49430360-49463191",
                            "ensembl_id": "ENSG00000146085"
                        }
                    }
                },
                "hgnc_date_symbol_changed": "2001-06-22"
            },
            "entity_type": "gene",
            "entity_name": "MUT",
            "confidence_level": "3",
            "penetrance": null,
            "mode_of_pathogenicity": "",
            "publications": [
                "20301409",
                "37420116",
                "1977311",
                "11528502",
                "12948746"
            ],
            "evidence": [
                "Expert Review Green",
                "Genetic Health Queensland"
            ],
            "phenotypes": [
                "Methylmalonic aciduria, mut(0) type, MIM# 251000"
            ],
            "mode_of_inheritance": "BIALLELIC, autosomal or pseudoautosomal",
            "tags": [
                "treatable"
            ],
            "panel": {
                "id": 250,
                "hash_id": null,
                "name": "Intellectual disability syndromic and non-syndromic",
                "disease_group": "Neurology and neurodevelopmental disorders",
                "disease_sub_group": "",
                "description": "This panel was created by merging the ID panels used by Genetic Health Queensland and by the Victorian Clinical Genetics Services. Discrepant gene classifications reviewed and resolved by Chirag Patel and Zornitza Stark.\r\n\r\nThis is a consensus panel used by VCGS, GHQ and RMH.\r\n\r\nThis panel has been compared against the Genomics England PanelApp Intellectual Disability panel, and all discrepancies have been resolved, with reciprocal reviews provided to Genomics England, 11/3/2020.",
                "status": "public",
                "version": "1.760",
                "version_created": "2026-04-26T17:50:23.271073+10:00",
                "relevant_disorders": [
                    "Intellectual disability",
                    "HP:0001249; Neurodevelopmental delay",
                    "HP:0012758"
                ],
                "stats": {
                    "number_of_genes": 2524,
                    "number_of_strs": 10,
                    "number_of_regions": 57
                },
                "types": [
                    {
                        "name": "Genetic Health Queensland",
                        "slug": "genetic-health-queensland",
                        "description": "Panel used by GHQ."
                    },
                    {
                        "name": "Victorian Clinical Genetics Services",
                        "slug": "victorian-clinical-genetics-services",
                        "description": "Panel used by VCGS."
                    },
                    {
                        "name": "Rare Disease",
                        "slug": "rare-disease",
                        "description": "Rare disease panels"
                    },
                    {
                        "name": "Royal Melbourne Hospital",
                        "slug": "royal-melbourne-hospital",
                        "description": "Royal Melbourne Hospital"
                    }
                ],
                "child_panel_ids": []
            },
            "transcript": null
        },
        {
            "gene_data": {
                "alias": [
                    "LRBP",
                    "MK"
                ],
                "biotype": "protein_coding",
                "hgnc_id": "HGNC:7530",
                "gene_name": "mevalonate kinase",
                "omim_gene": [
                    "251170"
                ],
                "alias_name": [
                    "LH receptor mRNA-binding protein",
                    "mevalonic aciduria"
                ],
                "gene_symbol": "MVK",
                "hgnc_symbol": "MVK",
                "hgnc_release": "2017-11-03",
                "ensembl_genes": {
                    "GRch37": {
                        "82": {
                            "location": "12:110011060-110035067",
                            "ensembl_id": "ENSG00000110921"
                        }
                    },
                    "GRch38": {
                        "90": {
                            "location": "12:109573255-109598117",
                            "ensembl_id": "ENSG00000110921"
                        }
                    }
                },
                "hgnc_date_symbol_changed": "1992-10-06"
            },
            "entity_type": "gene",
            "entity_name": "MVK",
            "confidence_level": "3",
            "penetrance": null,
            "mode_of_pathogenicity": "",
            "publications": [
                "29047407",
                "26409462"
            ],
            "evidence": [
                "Expert Review Green",
                "Genetic Health Queensland"
            ],
            "phenotypes": [
                "Hyper-IgD syndrome (MIM#260920)",
                "Mevalonic aciduria (MIM#610377)"
            ],
            "mode_of_inheritance": "BIALLELIC, autosomal or pseudoautosomal",
            "tags": [],
            "panel": {
                "id": 250,
                "hash_id": null,
                "name": "Intellectual disability syndromic and non-syndromic",
                "disease_group": "Neurology and neurodevelopmental disorders",
                "disease_sub_group": "",
                "description": "This panel was created by merging the ID panels used by Genetic Health Queensland and by the Victorian Clinical Genetics Services. Discrepant gene classifications reviewed and resolved by Chirag Patel and Zornitza Stark.\r\n\r\nThis is a consensus panel used by VCGS, GHQ and RMH.\r\n\r\nThis panel has been compared against the Genomics England PanelApp Intellectual Disability panel, and all discrepancies have been resolved, with reciprocal reviews provided to Genomics England, 11/3/2020.",
                "status": "public",
                "version": "1.760",
                "version_created": "2026-04-26T17:50:23.271073+10:00",
                "relevant_disorders": [
                    "Intellectual disability",
                    "HP:0001249; Neurodevelopmental delay",
                    "HP:0012758"
                ],
                "stats": {
                    "number_of_genes": 2524,
                    "number_of_strs": 10,
                    "number_of_regions": 57
                },
                "types": [
                    {
                        "name": "Genetic Health Queensland",
                        "slug": "genetic-health-queensland",
                        "description": "Panel used by GHQ."
                    },
                    {
                        "name": "Victorian Clinical Genetics Services",
                        "slug": "victorian-clinical-genetics-services",
                        "description": "Panel used by VCGS."
                    },
                    {
                        "name": "Rare Disease",
                        "slug": "rare-disease",
                        "description": "Rare disease panels"
                    },
                    {
                        "name": "Royal Melbourne Hospital",
                        "slug": "royal-melbourne-hospital",
                        "description": "Royal Melbourne Hospital"
                    }
                ],
                "child_panel_ids": []
            },
            "transcript": null
        },
        {
            "gene_data": {
                "alias": [
                    "bHLHe37",
                    "N-myc",
                    "MYCNOT"
                ],
                "biotype": "protein_coding",
                "hgnc_id": "HGNC:7559",
                "gene_name": "MYCN proto-oncogene, bHLH transcription factor",
                "omim_gene": [
                    "164840"
                ],
                "alias_name": null,
                "gene_symbol": "MYCN",
                "hgnc_symbol": "MYCN",
                "hgnc_release": "2017-11-03",
                "ensembl_genes": {
                    "GRch37": {
                        "82": {
                            "location": "2:16080686-16087129",
                            "ensembl_id": "ENSG00000134323"
                        }
                    },
                    "GRch38": {
                        "90": {
                            "location": "2:15940564-15947007",
                            "ensembl_id": "ENSG00000134323"
                        }
                    }
                },
                "hgnc_date_symbol_changed": "2001-06-22"
            },
            "entity_type": "gene",
            "entity_name": "MYCN",
            "confidence_level": "3",
            "penetrance": null,
            "mode_of_pathogenicity": "",
            "publications": [
                "37710961"
            ],
            "evidence": [
                "Expert Review Green",
                "Genetic Health Queensland"
            ],
            "phenotypes": [
                "Feingold syndrome 1 MIM#164280",
                "Megalencephaly-polydactyly syndrome, MIM#\t620748"
            ],
            "mode_of_inheritance": "MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted",
            "tags": [],
            "panel": {
                "id": 250,
                "hash_id": null,
                "name": "Intellectual disability syndromic and non-syndromic",
                "disease_group": "Neurology and neurodevelopmental disorders",
                "disease_sub_group": "",
                "description": "This panel was created by merging the ID panels used by Genetic Health Queensland and by the Victorian Clinical Genetics Services. Discrepant gene classifications reviewed and resolved by Chirag Patel and Zornitza Stark.\r\n\r\nThis is a consensus panel used by VCGS, GHQ and RMH.\r\n\r\nThis panel has been compared against the Genomics England PanelApp Intellectual Disability panel, and all discrepancies have been resolved, with reciprocal reviews provided to Genomics England, 11/3/2020.",
                "status": "public",
                "version": "1.760",
                "version_created": "2026-04-26T17:50:23.271073+10:00",
                "relevant_disorders": [
                    "Intellectual disability",
                    "HP:0001249; Neurodevelopmental delay",
                    "HP:0012758"
                ],
                "stats": {
                    "number_of_genes": 2524,
                    "number_of_strs": 10,
                    "number_of_regions": 57
                },
                "types": [
                    {
                        "name": "Genetic Health Queensland",
                        "slug": "genetic-health-queensland",
                        "description": "Panel used by GHQ."
                    },
                    {
                        "name": "Victorian Clinical Genetics Services",
                        "slug": "victorian-clinical-genetics-services",
                        "description": "Panel used by VCGS."
                    },
                    {
                        "name": "Rare Disease",
                        "slug": "rare-disease",
                        "description": "Rare disease panels"
                    },
                    {
                        "name": "Royal Melbourne Hospital",
                        "slug": "royal-melbourne-hospital",
                        "description": "Royal Melbourne Hospital"
                    }
                ],
                "child_panel_ids": []
            },
            "transcript": null
        },
        {
            "gene_data": {
                "alias": [
                    "MYHC-EMB",
                    "MYHSE1",
                    "HEMHC",
                    "SMHCE"
                ],
                "biotype": "protein_coding",
                "hgnc_id": "HGNC:7573",
                "gene_name": "myosin heavy chain 3",
                "omim_gene": [
                    "160720"
                ],
                "alias_name": [
                    "myosin, skeletal, heavy chain, embryonic 1",
                    "muscle embryonic myosin heavy chain 3"
                ],
                "gene_symbol": "MYH3",
                "hgnc_symbol": "MYH3",
                "hgnc_release": "2017-11-03",
                "ensembl_genes": {
                    "GRch37": {
                        "82": {
                            "location": "17:10531843-10560626",
                            "ensembl_id": "ENSG00000109063"
                        }
                    },
                    "GRch38": {
                        "90": {
                            "location": "17:10628526-10657309",
                            "ensembl_id": "ENSG00000109063"
                        }
                    }
                },
                "hgnc_date_symbol_changed": "2001-06-22"
            },
            "entity_type": "gene",
            "entity_name": "MYH3",
            "confidence_level": "1",
            "penetrance": null,
            "mode_of_pathogenicity": "",
            "publications": [],
            "evidence": [
                "Expert Review Red",
                "Expert list"
            ],
            "phenotypes": [
                "Arthrogryposis, distal, type 2A (Freeman-Sheldon), OMIM #193700",
                "Arthrogryposis, distal, type 2B3 (Sheldon-Hall), OMIM #618436",
                "Contractures, pterygia, and variable skeletal fusions syndrome 1A, OMIM #178110",
                "Contractures, pterygia, and variable skeletal fusions syndrome 1B, OMIM #618469"
            ],
            "mode_of_inheritance": "BOTH monoallelic and biallelic, autosomal or pseudoautosomal",
            "tags": [],
            "panel": {
                "id": 250,
                "hash_id": null,
                "name": "Intellectual disability syndromic and non-syndromic",
                "disease_group": "Neurology and neurodevelopmental disorders",
                "disease_sub_group": "",
                "description": "This panel was created by merging the ID panels used by Genetic Health Queensland and by the Victorian Clinical Genetics Services. Discrepant gene classifications reviewed and resolved by Chirag Patel and Zornitza Stark.\r\n\r\nThis is a consensus panel used by VCGS, GHQ and RMH.\r\n\r\nThis panel has been compared against the Genomics England PanelApp Intellectual Disability panel, and all discrepancies have been resolved, with reciprocal reviews provided to Genomics England, 11/3/2020.",
                "status": "public",
                "version": "1.760",
                "version_created": "2026-04-26T17:50:23.271073+10:00",
                "relevant_disorders": [
                    "Intellectual disability",
                    "HP:0001249; Neurodevelopmental delay",
                    "HP:0012758"
                ],
                "stats": {
                    "number_of_genes": 2524,
                    "number_of_strs": 10,
                    "number_of_regions": 57
                },
                "types": [
                    {
                        "name": "Genetic Health Queensland",
                        "slug": "genetic-health-queensland",
                        "description": "Panel used by GHQ."
                    },
                    {
                        "name": "Victorian Clinical Genetics Services",
                        "slug": "victorian-clinical-genetics-services",
                        "description": "Panel used by VCGS."
                    },
                    {
                        "name": "Rare Disease",
                        "slug": "rare-disease",
                        "description": "Rare disease panels"
                    },
                    {
                        "name": "Royal Melbourne Hospital",
                        "slug": "royal-melbourne-hospital",
                        "description": "Royal Melbourne Hospital"
                    }
                ],
                "child_panel_ids": []
            },
            "transcript": null
        },
        {
            "gene_data": {
                "alias": [
                    "MYO5",
                    "GS1",
                    "MYR12"
                ],
                "biotype": "protein_coding",
                "hgnc_id": "HGNC:7602",
                "gene_name": "myosin VA",
                "omim_gene": [
                    "160777"
                ],
                "alias_name": [
                    "myosin, heavy polypeptide kinase",
                    "myosin heavy chain 12",
                    "myoxin",
                    "myosin V"
                ],
                "gene_symbol": "MYO5A",
                "hgnc_symbol": "MYO5A",
                "hgnc_release": "2017-11-03",
                "ensembl_genes": {
                    "GRch37": {
                        "82": {
                            "location": "15:52599480-52821247",
                            "ensembl_id": "ENSG00000197535"
                        }
                    },
                    "GRch38": {
                        "90": {
                            "location": "15:52307283-52529050",
                            "ensembl_id": "ENSG00000197535"
                        }
                    }
                },
                "hgnc_date_symbol_changed": "1993-09-23"
            },
            "entity_type": "gene",
            "entity_name": "MYO5A",
            "confidence_level": "3",
            "penetrance": null,
            "mode_of_pathogenicity": "",
            "publications": [
                "32275080",
                "22711375",
                "25283056"
            ],
            "evidence": [
                "Expert Review Green",
                "Genetic Health Queensland"
            ],
            "phenotypes": [
                "Griscelli syndrome, type 1 MIM#214450"
            ],
            "mode_of_inheritance": "BIALLELIC, autosomal or pseudoautosomal",
            "tags": [],
            "panel": {
                "id": 250,
                "hash_id": null,
                "name": "Intellectual disability syndromic and non-syndromic",
                "disease_group": "Neurology and neurodevelopmental disorders",
                "disease_sub_group": "",
                "description": "This panel was created by merging the ID panels used by Genetic Health Queensland and by the Victorian Clinical Genetics Services. Discrepant gene classifications reviewed and resolved by Chirag Patel and Zornitza Stark.\r\n\r\nThis is a consensus panel used by VCGS, GHQ and RMH.\r\n\r\nThis panel has been compared against the Genomics England PanelApp Intellectual Disability panel, and all discrepancies have been resolved, with reciprocal reviews provided to Genomics England, 11/3/2020.",
                "status": "public",
                "version": "1.760",
                "version_created": "2026-04-26T17:50:23.271073+10:00",
                "relevant_disorders": [
                    "Intellectual disability",
                    "HP:0001249; Neurodevelopmental delay",
                    "HP:0012758"
                ],
                "stats": {
                    "number_of_genes": 2524,
                    "number_of_strs": 10,
                    "number_of_regions": 57
                },
                "types": [
                    {
                        "name": "Genetic Health Queensland",
                        "slug": "genetic-health-queensland",
                        "description": "Panel used by GHQ."
                    },
                    {
                        "name": "Victorian Clinical Genetics Services",
                        "slug": "victorian-clinical-genetics-services",
                        "description": "Panel used by VCGS."
                    },
                    {
                        "name": "Rare Disease",
                        "slug": "rare-disease",
                        "description": "Rare disease panels"
                    },
                    {
                        "name": "Royal Melbourne Hospital",
                        "slug": "royal-melbourne-hospital",
                        "description": "Royal Melbourne Hospital"
                    }
                ],
                "child_panel_ids": []
            },
            "transcript": null
        },
        {
            "gene_data": {
                "alias": [
                    "NSRD2"
                ],
                "biotype": "protein_coding",
                "hgnc_id": "HGNC:7606",
                "gene_name": "myosin VIIA",
                "omim_gene": [
                    "276903"
                ],
                "alias_name": null,
                "gene_symbol": "MYO7A",
                "hgnc_symbol": "MYO7A",
                "hgnc_release": "2017-11-03",
                "ensembl_genes": {
                    "GRch37": {
                        "82": {
                            "location": "11:76839310-76926284",
                            "ensembl_id": "ENSG00000137474"
                        }
                    },
                    "GRch38": {
                        "90": {
                            "location": "11:77128264-77215239",
                            "ensembl_id": "ENSG00000137474"
                        }
                    }
                },
                "hgnc_date_symbol_changed": "1992-06-08"
            },
            "entity_type": "gene",
            "entity_name": "MYO7A",
            "confidence_level": "1",
            "penetrance": null,
            "mode_of_pathogenicity": "",
            "publications": [],
            "evidence": [
                "Expert Review Red",
                "Expert list"
            ],
            "phenotypes": [
                "Deafness, autosomal dominant 11, OMIM #601317",
                "Deafness, autosomal recessive 2, OMIM #600060",
                "Usher syndrome, type 1B, OMIM #276900"
            ],
            "mode_of_inheritance": "BOTH monoallelic and biallelic, autosomal or pseudoautosomal",
            "tags": [],
            "panel": {
                "id": 250,
                "hash_id": null,
                "name": "Intellectual disability syndromic and non-syndromic",
                "disease_group": "Neurology and neurodevelopmental disorders",
                "disease_sub_group": "",
                "description": "This panel was created by merging the ID panels used by Genetic Health Queensland and by the Victorian Clinical Genetics Services. Discrepant gene classifications reviewed and resolved by Chirag Patel and Zornitza Stark.\r\n\r\nThis is a consensus panel used by VCGS, GHQ and RMH.\r\n\r\nThis panel has been compared against the Genomics England PanelApp Intellectual Disability panel, and all discrepancies have been resolved, with reciprocal reviews provided to Genomics England, 11/3/2020.",
                "status": "public",
                "version": "1.760",
                "version_created": "2026-04-26T17:50:23.271073+10:00",
                "relevant_disorders": [
                    "Intellectual disability",
                    "HP:0001249; Neurodevelopmental delay",
                    "HP:0012758"
                ],
                "stats": {
                    "number_of_genes": 2524,
                    "number_of_strs": 10,
                    "number_of_regions": 57
                },
                "types": [
                    {
                        "name": "Genetic Health Queensland",
                        "slug": "genetic-health-queensland",
                        "description": "Panel used by GHQ."
                    },
                    {
                        "name": "Victorian Clinical Genetics Services",
                        "slug": "victorian-clinical-genetics-services",
                        "description": "Panel used by VCGS."
                    },
                    {
                        "name": "Rare Disease",
                        "slug": "rare-disease",
                        "description": "Rare disease panels"
                    },
                    {
                        "name": "Royal Melbourne Hospital",
                        "slug": "royal-melbourne-hospital",
                        "description": "Royal Melbourne Hospital"
                    }
                ],
                "child_panel_ids": []
            },
            "transcript": null
        },
        {
            "gene_data": {
                "alias": [
                    "KIAA1106",
                    "NZF1",
                    "ZC2HC4B",
                    "ZC2H2C2"
                ],
                "biotype": "protein_coding",
                "hgnc_id": "HGNC:7623",
                "gene_name": "myelin transcription factor 1 like",
                "omim_gene": [
                    "613084"
                ],
                "alias_name": [
                    "neural zinc finger transcription factor 1"
                ],
                "gene_symbol": "MYT1L",
                "hgnc_symbol": "MYT1L",
                "hgnc_release": "2017-11-03",
                "ensembl_genes": {
                    "GRch37": {
                        "82": {
                            "location": "2:1792885-2335032",
                            "ensembl_id": "ENSG00000186487"
                        }
                    },
                    "GRch38": {
                        "90": {
                            "location": "2:1789113-2331260",
                            "ensembl_id": "ENSG00000186487"
                        }
                    }
                },
                "hgnc_date_symbol_changed": "1996-07-11"
            },
            "entity_type": "gene",
            "entity_name": "MYT1L",
            "confidence_level": "3",
            "penetrance": null,
            "mode_of_pathogenicity": "",
            "publications": [
                "28859103",
                "32065501"
            ],
            "evidence": [
                "Expert Review Green",
                "Genetic Health Queensland"
            ],
            "phenotypes": [
                "Mental retardation, autosomal dominant 39, MIM# 616521"
            ],
            "mode_of_inheritance": "MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted",
            "tags": [
                "SV/CNV"
            ],
            "panel": {
                "id": 250,
                "hash_id": null,
                "name": "Intellectual disability syndromic and non-syndromic",
                "disease_group": "Neurology and neurodevelopmental disorders",
                "disease_sub_group": "",
                "description": "This panel was created by merging the ID panels used by Genetic Health Queensland and by the Victorian Clinical Genetics Services. Discrepant gene classifications reviewed and resolved by Chirag Patel and Zornitza Stark.\r\n\r\nThis is a consensus panel used by VCGS, GHQ and RMH.\r\n\r\nThis panel has been compared against the Genomics England PanelApp Intellectual Disability panel, and all discrepancies have been resolved, with reciprocal reviews provided to Genomics England, 11/3/2020.",
                "status": "public",
                "version": "1.760",
                "version_created": "2026-04-26T17:50:23.271073+10:00",
                "relevant_disorders": [
                    "Intellectual disability",
                    "HP:0001249; Neurodevelopmental delay",
                    "HP:0012758"
                ],
                "stats": {
                    "number_of_genes": 2524,
                    "number_of_strs": 10,
                    "number_of_regions": 57
                },
                "types": [
                    {
                        "name": "Genetic Health Queensland",
                        "slug": "genetic-health-queensland",
                        "description": "Panel used by GHQ."
                    },
                    {
                        "name": "Victorian Clinical Genetics Services",
                        "slug": "victorian-clinical-genetics-services",
                        "description": "Panel used by VCGS."
                    },
                    {
                        "name": "Rare Disease",
                        "slug": "rare-disease",
                        "description": "Rare disease panels"
                    },
                    {
                        "name": "Royal Melbourne Hospital",
                        "slug": "royal-melbourne-hospital",
                        "description": "Royal Melbourne Hospital"
                    }
                ],
                "child_panel_ids": []
            },
            "transcript": null
        },
        {
            "gene_data": {
                "alias": [
                    "DXS707",
                    "TE2"
                ],
                "biotype": "protein_coding",
                "hgnc_id": "HGNC:18704",
                "gene_name": "N(alpha)-acetyltransferase 10, NatA catalytic subunit",
                "omim_gene": [
                    "300013"
                ],
                "alias_name": null,
                "gene_symbol": "NAA10",
                "hgnc_symbol": "NAA10",
                "hgnc_release": "2017-11-03",
                "ensembl_genes": {
                    "GRch37": {
                        "82": {
                            "location": "X:153194695-153200676",
                            "ensembl_id": "ENSG00000102030"
                        }
                    },
                    "GRch38": {
                        "90": {
                            "location": "X:153929242-153935223",
                            "ensembl_id": "ENSG00000102030"
                        }
                    }
                },
                "hgnc_date_symbol_changed": "2010-01-14"
            },
            "entity_type": "gene",
            "entity_name": "NAA10",
            "confidence_level": "3",
            "penetrance": null,
            "mode_of_pathogenicity": "",
            "publications": [
                "30842225",
                "34075687",
                "21700266"
            ],
            "evidence": [
                "Expert Review Green",
                "Genetic Health Queensland"
            ],
            "phenotypes": [
                "Microphthalmia, syndromic 1, MIM# 309800",
                "Ogden syndrome MIM#300855"
            ],
            "mode_of_inheritance": "X-LINKED: hemizygous mutation in males, monoallelic mutations in females may cause disease (may be less severe, later onset than males)",
            "tags": [
                "5'UTR"
            ],
            "panel": {
                "id": 250,
                "hash_id": null,
                "name": "Intellectual disability syndromic and non-syndromic",
                "disease_group": "Neurology and neurodevelopmental disorders",
                "disease_sub_group": "",
                "description": "This panel was created by merging the ID panels used by Genetic Health Queensland and by the Victorian Clinical Genetics Services. Discrepant gene classifications reviewed and resolved by Chirag Patel and Zornitza Stark.\r\n\r\nThis is a consensus panel used by VCGS, GHQ and RMH.\r\n\r\nThis panel has been compared against the Genomics England PanelApp Intellectual Disability panel, and all discrepancies have been resolved, with reciprocal reviews provided to Genomics England, 11/3/2020.",
                "status": "public",
                "version": "1.760",
                "version_created": "2026-04-26T17:50:23.271073+10:00",
                "relevant_disorders": [
                    "Intellectual disability",
                    "HP:0001249; Neurodevelopmental delay",
                    "HP:0012758"
                ],
                "stats": {
                    "number_of_genes": 2524,
                    "number_of_strs": 10,
                    "number_of_regions": 57
                },
                "types": [
                    {
                        "name": "Genetic Health Queensland",
                        "slug": "genetic-health-queensland",
                        "description": "Panel used by GHQ."
                    },
                    {
                        "name": "Victorian Clinical Genetics Services",
                        "slug": "victorian-clinical-genetics-services",
                        "description": "Panel used by VCGS."
                    },
                    {
                        "name": "Rare Disease",
                        "slug": "rare-disease",
                        "description": "Rare disease panels"
                    },
                    {
                        "name": "Royal Melbourne Hospital",
                        "slug": "royal-melbourne-hospital",
                        "description": "Royal Melbourne Hospital"
                    }
                ],
                "child_panel_ids": []
            },
            "transcript": null
        },
        {
            "gene_data": {
                "alias": [
                    "D22S674"
                ],
                "biotype": "protein_coding",
                "hgnc_id": "HGNC:7631",
                "gene_name": "alpha-N-acetylgalactosaminidase",
                "omim_gene": [
                    "104170"
                ],
                "alias_name": null,
                "gene_symbol": "NAGA",
                "hgnc_symbol": "NAGA",
                "hgnc_release": "2017-11-03",
                "ensembl_genes": {
                    "GRch37": {
                        "82": {
                            "location": "22:42454358-42466846",
                            "ensembl_id": "ENSG00000198951"
                        }
                    },
                    "GRch38": {
                        "90": {
                            "location": "22:42058354-42070842",
                            "ensembl_id": "ENSG00000198951"
                        }
                    }
                },
                "hgnc_date_symbol_changed": "1986-01-01"
            },
            "entity_type": "gene",
            "entity_name": "NAGA",
            "confidence_level": "3",
            "penetrance": null,
            "mode_of_pathogenicity": "",
            "publications": [
                "11313741",
                "31468281",
                "15619430",
                "8782044"
            ],
            "evidence": [
                "Expert Review Green",
                "Genetic Health Queensland"
            ],
            "phenotypes": [
                "Kanzaki disease, MIM# 609242",
                "Schindler disease, type I and type II 609241",
                "alpha-N-acetylgalactosaminidase deficiency MONDO:0017779"
            ],
            "mode_of_inheritance": "BIALLELIC, autosomal or pseudoautosomal",
            "tags": [],
            "panel": {
                "id": 250,
                "hash_id": null,
                "name": "Intellectual disability syndromic and non-syndromic",
                "disease_group": "Neurology and neurodevelopmental disorders",
                "disease_sub_group": "",
                "description": "This panel was created by merging the ID panels used by Genetic Health Queensland and by the Victorian Clinical Genetics Services. Discrepant gene classifications reviewed and resolved by Chirag Patel and Zornitza Stark.\r\n\r\nThis is a consensus panel used by VCGS, GHQ and RMH.\r\n\r\nThis panel has been compared against the Genomics England PanelApp Intellectual Disability panel, and all discrepancies have been resolved, with reciprocal reviews provided to Genomics England, 11/3/2020.",
                "status": "public",
                "version": "1.760",
                "version_created": "2026-04-26T17:50:23.271073+10:00",
                "relevant_disorders": [
                    "Intellectual disability",
                    "HP:0001249; Neurodevelopmental delay",
                    "HP:0012758"
                ],
                "stats": {
                    "number_of_genes": 2524,
                    "number_of_strs": 10,
                    "number_of_regions": 57
                },
                "types": [
                    {
                        "name": "Genetic Health Queensland",
                        "slug": "genetic-health-queensland",
                        "description": "Panel used by GHQ."
                    },
                    {
                        "name": "Victorian Clinical Genetics Services",
                        "slug": "victorian-clinical-genetics-services",
                        "description": "Panel used by VCGS."
                    },
                    {
                        "name": "Rare Disease",
                        "slug": "rare-disease",
                        "description": "Rare disease panels"
                    },
                    {
                        "name": "Royal Melbourne Hospital",
                        "slug": "royal-melbourne-hospital",
                        "description": "Royal Melbourne Hospital"
                    }
                ],
                "child_panel_ids": []
            },
            "transcript": null
        },
        {
            "gene_data": {
                "alias": [
                    "NAG"
                ],
                "biotype": "protein_coding",
                "hgnc_id": "HGNC:7632",
                "gene_name": "N-acetyl-alpha-glucosaminidase",
                "omim_gene": [
                    "609701"
                ],
                "alias_name": [
                    "Sanfilippo disease IIIB"
                ],
                "gene_symbol": "NAGLU",
                "hgnc_symbol": "NAGLU",
                "hgnc_release": "2017-11-03",
                "ensembl_genes": {
                    "GRch37": {
                        "82": {
                            "location": "17:40688190-40696467",
                            "ensembl_id": "ENSG00000108784"
                        }
                    },
                    "GRch38": {
                        "90": {
                            "location": "17:42536172-42544449",
                            "ensembl_id": "ENSG00000108784"
                        }
                    }
                },
                "hgnc_date_symbol_changed": "1995-09-15"
            },
            "entity_type": "gene",
            "entity_name": "NAGLU",
            "confidence_level": "3",
            "penetrance": null,
            "mode_of_pathogenicity": "",
            "publications": [
                "8650226"
            ],
            "evidence": [
                "Expert Review Green",
                "Genetic Health Queensland"
            ],
            "phenotypes": [
                "Mucopolysaccharidosis type IIIB (Sanfilippo B), MIM# 252920"
            ],
            "mode_of_inheritance": "BIALLELIC, autosomal or pseudoautosomal",
            "tags": [],
            "panel": {
                "id": 250,
                "hash_id": null,
                "name": "Intellectual disability syndromic and non-syndromic",
                "disease_group": "Neurology and neurodevelopmental disorders",
                "disease_sub_group": "",
                "description": "This panel was created by merging the ID panels used by Genetic Health Queensland and by the Victorian Clinical Genetics Services. Discrepant gene classifications reviewed and resolved by Chirag Patel and Zornitza Stark.\r\n\r\nThis is a consensus panel used by VCGS, GHQ and RMH.\r\n\r\nThis panel has been compared against the Genomics England PanelApp Intellectual Disability panel, and all discrepancies have been resolved, with reciprocal reviews provided to Genomics England, 11/3/2020.",
                "status": "public",
                "version": "1.760",
                "version_created": "2026-04-26T17:50:23.271073+10:00",
                "relevant_disorders": [
                    "Intellectual disability",
                    "HP:0001249; Neurodevelopmental delay",
                    "HP:0012758"
                ],
                "stats": {
                    "number_of_genes": 2524,
                    "number_of_strs": 10,
                    "number_of_regions": 57
                },
                "types": [
                    {
                        "name": "Genetic Health Queensland",
                        "slug": "genetic-health-queensland",
                        "description": "Panel used by GHQ."
                    },
                    {
                        "name": "Victorian Clinical Genetics Services",
                        "slug": "victorian-clinical-genetics-services",
                        "description": "Panel used by VCGS."
                    },
                    {
                        "name": "Rare Disease",
                        "slug": "rare-disease",
                        "description": "Rare disease panels"
                    },
                    {
                        "name": "Royal Melbourne Hospital",
                        "slug": "royal-melbourne-hospital",
                        "description": "Royal Melbourne Hospital"
                    }
                ],
                "child_panel_ids": []
            },
            "transcript": null
        },
        {
            "gene_data": {
                "alias": [
                    "AGAS",
                    "ARGA",
                    "NAT7"
                ],
                "biotype": "protein_coding",
                "hgnc_id": "HGNC:17996",
                "gene_name": "N-acetylglutamate synthase",
                "omim_gene": [
                    "608300"
                ],
                "alias_name": null,
                "gene_symbol": "NAGS",
                "hgnc_symbol": "NAGS",
                "hgnc_release": "2017-11-03",
                "ensembl_genes": {
                    "GRch37": {
                        "82": {
                            "location": "17:42081914-42086431",
                            "ensembl_id": "ENSG00000161653"
                        }
                    },
                    "GRch38": {
                        "90": {
                            "location": "17:44004546-44009063",
                            "ensembl_id": "ENSG00000161653"
                        }
                    }
                },
                "hgnc_date_symbol_changed": "2004-12-03"
            },
            "entity_type": "gene",
            "entity_name": "NAGS",
            "confidence_level": "1",
            "penetrance": null,
            "mode_of_pathogenicity": "",
            "publications": [],
            "evidence": [
                "Expert Review Red",
                "Genetic Health Queensland"
            ],
            "phenotypes": [
                "N-acetylglutamate synthase deficiency, MIM#237310"
            ],
            "mode_of_inheritance": "BIALLELIC, autosomal or pseudoautosomal",
            "tags": [],
            "panel": {
                "id": 250,
                "hash_id": null,
                "name": "Intellectual disability syndromic and non-syndromic",
                "disease_group": "Neurology and neurodevelopmental disorders",
                "disease_sub_group": "",
                "description": "This panel was created by merging the ID panels used by Genetic Health Queensland and by the Victorian Clinical Genetics Services. Discrepant gene classifications reviewed and resolved by Chirag Patel and Zornitza Stark.\r\n\r\nThis is a consensus panel used by VCGS, GHQ and RMH.\r\n\r\nThis panel has been compared against the Genomics England PanelApp Intellectual Disability panel, and all discrepancies have been resolved, with reciprocal reviews provided to Genomics England, 11/3/2020.",
                "status": "public",
                "version": "1.760",
                "version_created": "2026-04-26T17:50:23.271073+10:00",
                "relevant_disorders": [
                    "Intellectual disability",
                    "HP:0001249; Neurodevelopmental delay",
                    "HP:0012758"
                ],
                "stats": {
                    "number_of_genes": 2524,
                    "number_of_strs": 10,
                    "number_of_regions": 57
                },
                "types": [
                    {
                        "name": "Genetic Health Queensland",
                        "slug": "genetic-health-queensland",
                        "description": "Panel used by GHQ."
                    },
                    {
                        "name": "Victorian Clinical Genetics Services",
                        "slug": "victorian-clinical-genetics-services",
                        "description": "Panel used by VCGS."
                    },
                    {
                        "name": "Rare Disease",
                        "slug": "rare-disease",
                        "description": "Rare disease panels"
                    },
                    {
                        "name": "Royal Melbourne Hospital",
                        "slug": "royal-melbourne-hospital",
                        "description": "Royal Melbourne Hospital"
                    }
                ],
                "child_panel_ids": []
            },
            "transcript": null
        },
        {
            "gene_data": {
                "alias": [
                    "bA430M15.1",
                    "CanIon"
                ],
                "biotype": "protein_coding",
                "hgnc_id": "HGNC:19082",
                "gene_name": "sodium leak channel, non-selective",
                "omim_gene": [
                    "611549"
                ],
                "alias_name": null,
                "gene_symbol": "NALCN",
                "hgnc_symbol": "NALCN",
                "hgnc_release": "2017-11-03",
                "ensembl_genes": {
                    "GRch37": {
                        "82": {
                            "location": "13:101706130-102068843",
                            "ensembl_id": "ENSG00000102452"
                        }
                    },
                    "GRch38": {
                        "90": {
                            "location": "13:101053776-101416492",
                            "ensembl_id": "ENSG00000102452"
                        }
                    }
                },
                "hgnc_date_symbol_changed": "2007-04-26"
            },
            "entity_type": "gene",
            "entity_name": "NALCN",
            "confidence_level": "3",
            "penetrance": null,
            "mode_of_pathogenicity": "",
            "publications": [
                "25683120",
                "30167850",
                "23749988",
                "24075186"
            ],
            "evidence": [
                "Expert Review Green",
                "Genetic Health Queensland"
            ],
            "phenotypes": [
                "Congenital contractures of the limbs and face, hypotonia, and developmental delay, MIM# 616266",
                "Hypotonia, infantile, with psychomotor retardation and characteristic facies 1, MIM # 615419"
            ],
            "mode_of_inheritance": "BOTH monoallelic and biallelic, autosomal or pseudoautosomal",
            "tags": [],
            "panel": {
                "id": 250,
                "hash_id": null,
                "name": "Intellectual disability syndromic and non-syndromic",
                "disease_group": "Neurology and neurodevelopmental disorders",
                "disease_sub_group": "",
                "description": "This panel was created by merging the ID panels used by Genetic Health Queensland and by the Victorian Clinical Genetics Services. Discrepant gene classifications reviewed and resolved by Chirag Patel and Zornitza Stark.\r\n\r\nThis is a consensus panel used by VCGS, GHQ and RMH.\r\n\r\nThis panel has been compared against the Genomics England PanelApp Intellectual Disability panel, and all discrepancies have been resolved, with reciprocal reviews provided to Genomics England, 11/3/2020.",
                "status": "public",
                "version": "1.760",
                "version_created": "2026-04-26T17:50:23.271073+10:00",
                "relevant_disorders": [
                    "Intellectual disability",
                    "HP:0001249; Neurodevelopmental delay",
                    "HP:0012758"
                ],
                "stats": {
                    "number_of_genes": 2524,
                    "number_of_strs": 10,
                    "number_of_regions": 57
                },
                "types": [
                    {
                        "name": "Genetic Health Queensland",
                        "slug": "genetic-health-queensland",
                        "description": "Panel used by GHQ."
                    },
                    {
                        "name": "Victorian Clinical Genetics Services",
                        "slug": "victorian-clinical-genetics-services",
                        "description": "Panel used by VCGS."
                    },
                    {
                        "name": "Rare Disease",
                        "slug": "rare-disease",
                        "description": "Rare disease panels"
                    },
                    {
                        "name": "Royal Melbourne Hospital",
                        "slug": "royal-melbourne-hospital",
                        "description": "Royal Melbourne Hospital"
                    }
                ],
                "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": "2",
            "penetrance": null,
            "mode_of_pathogenicity": "",
            "publications": [],
            "evidence": [
                "Expert Review Amber",
                "Genetic Health Queensland"
            ],
            "phenotypes": [
                "Nijmegen breakage syndrome, MIM# 251260"
            ],
            "mode_of_inheritance": "BIALLELIC, autosomal or pseudoautosomal",
            "tags": [],
            "panel": {
                "id": 250,
                "hash_id": null,
                "name": "Intellectual disability syndromic and non-syndromic",
                "disease_group": "Neurology and neurodevelopmental disorders",
                "disease_sub_group": "",
                "description": "This panel was created by merging the ID panels used by Genetic Health Queensland and by the Victorian Clinical Genetics Services. Discrepant gene classifications reviewed and resolved by Chirag Patel and Zornitza Stark.\r\n\r\nThis is a consensus panel used by VCGS, GHQ and RMH.\r\n\r\nThis panel has been compared against the Genomics England PanelApp Intellectual Disability panel, and all discrepancies have been resolved, with reciprocal reviews provided to Genomics England, 11/3/2020.",
                "status": "public",
                "version": "1.760",
                "version_created": "2026-04-26T17:50:23.271073+10:00",
                "relevant_disorders": [
                    "Intellectual disability",
                    "HP:0001249; Neurodevelopmental delay",
                    "HP:0012758"
                ],
                "stats": {
                    "number_of_genes": 2524,
                    "number_of_strs": 10,
                    "number_of_regions": 57
                },
                "types": [
                    {
                        "name": "Genetic Health Queensland",
                        "slug": "genetic-health-queensland",
                        "description": "Panel used by GHQ."
                    },
                    {
                        "name": "Victorian Clinical Genetics Services",
                        "slug": "victorian-clinical-genetics-services",
                        "description": "Panel used by VCGS."
                    },
                    {
                        "name": "Rare Disease",
                        "slug": "rare-disease",
                        "description": "Rare disease panels"
                    },
                    {
                        "name": "Royal Melbourne Hospital",
                        "slug": "royal-melbourne-hospital",
                        "description": "Royal Melbourne Hospital"
                    }
                ],
                "child_panel_ids": []
            },
            "transcript": null
        },
        {
            "gene_data": {
                "alias": [
                    "nudE",
                    "FLJ20101",
                    "NDE"
                ],
                "biotype": "protein_coding",
                "hgnc_id": "HGNC:17619",
                "gene_name": "nudE neurodevelopment protein 1",
                "omim_gene": [
                    "609449"
                ],
                "alias_name": null,
                "gene_symbol": "NDE1",
                "hgnc_symbol": "NDE1",
                "hgnc_release": "2017-11-03",
                "ensembl_genes": {
                    "GRch37": {
                        "82": {
                            "location": "16:15737124-15820210",
                            "ensembl_id": "ENSG00000072864"
                        }
                    },
                    "GRch38": {
                        "90": {
                            "location": "16:15643267-15726353",
                            "ensembl_id": "ENSG00000072864"
                        }
                    }
                },
                "hgnc_date_symbol_changed": "2003-04-10"
            },
            "entity_type": "gene",
            "entity_name": "NDE1",
            "confidence_level": "3",
            "penetrance": null,
            "mode_of_pathogenicity": "",
            "publications": [
                "21529752",
                "21529751",
                "30637988",
                "15473967"
            ],
            "evidence": [
                "Expert Review Green",
                "Genetic Health Queensland"
            ],
            "phenotypes": [
                "Microcephaly with lissencephaly and/or hydranencephaly, MONDO:0700116"
            ],
            "mode_of_inheritance": "BIALLELIC, autosomal or pseudoautosomal",
            "tags": [],
            "panel": {
                "id": 250,
                "hash_id": null,
                "name": "Intellectual disability syndromic and non-syndromic",
                "disease_group": "Neurology and neurodevelopmental disorders",
                "disease_sub_group": "",
                "description": "This panel was created by merging the ID panels used by Genetic Health Queensland and by the Victorian Clinical Genetics Services. Discrepant gene classifications reviewed and resolved by Chirag Patel and Zornitza Stark.\r\n\r\nThis is a consensus panel used by VCGS, GHQ and RMH.\r\n\r\nThis panel has been compared against the Genomics England PanelApp Intellectual Disability panel, and all discrepancies have been resolved, with reciprocal reviews provided to Genomics England, 11/3/2020.",
                "status": "public",
                "version": "1.760",
                "version_created": "2026-04-26T17:50:23.271073+10:00",
                "relevant_disorders": [
                    "Intellectual disability",
                    "HP:0001249; Neurodevelopmental delay",
                    "HP:0012758"
                ],
                "stats": {
                    "number_of_genes": 2524,
                    "number_of_strs": 10,
                    "number_of_regions": 57
                },
                "types": [
                    {
                        "name": "Genetic Health Queensland",
                        "slug": "genetic-health-queensland",
                        "description": "Panel used by GHQ."
                    },
                    {
                        "name": "Victorian Clinical Genetics Services",
                        "slug": "victorian-clinical-genetics-services",
                        "description": "Panel used by VCGS."
                    },
                    {
                        "name": "Rare Disease",
                        "slug": "rare-disease",
                        "description": "Rare disease panels"
                    },
                    {
                        "name": "Royal Melbourne Hospital",
                        "slug": "royal-melbourne-hospital",
                        "description": "Royal Melbourne Hospital"
                    }
                ],
                "child_panel_ids": []
            },
            "transcript": null
        },
        {
            "gene_data": {
                "alias": [
                    "HsT16328",
                    "PWCR"
                ],
                "biotype": "protein_coding",
                "hgnc_id": "HGNC:7675",
                "gene_name": "necdin, MAGE family member",
                "omim_gene": [
                    "602117"
                ],
                "alias_name": [
                    "Prader-Willi syndrome chromosome region"
                ],
                "gene_symbol": "NDN",
                "hgnc_symbol": "NDN",
                "hgnc_release": "2017-11-03",
                "ensembl_genes": {
                    "GRch37": {
                        "82": {
                            "location": "15:23930565-23932450",
                            "ensembl_id": "ENSG00000182636"
                        }
                    },
                    "GRch38": {
                        "90": {
                            "location": "15:23685400-23687330",
                            "ensembl_id": "ENSG00000182636"
                        }
                    }
                },
                "hgnc_date_symbol_changed": "1997-10-13"
            },
            "entity_type": "gene",
            "entity_name": "NDN",
            "confidence_level": "1",
            "penetrance": null,
            "mode_of_pathogenicity": "",
            "publications": [],
            "evidence": [
                "Expert Review Red",
                "Genetic Health Queensland"
            ],
            "phenotypes": [
                "Prader-Willi syndrome, MIM#\t176270"
            ],
            "mode_of_inheritance": "Unknown",
            "tags": [],
            "panel": {
                "id": 250,
                "hash_id": null,
                "name": "Intellectual disability syndromic and non-syndromic",
                "disease_group": "Neurology and neurodevelopmental disorders",
                "disease_sub_group": "",
                "description": "This panel was created by merging the ID panels used by Genetic Health Queensland and by the Victorian Clinical Genetics Services. Discrepant gene classifications reviewed and resolved by Chirag Patel and Zornitza Stark.\r\n\r\nThis is a consensus panel used by VCGS, GHQ and RMH.\r\n\r\nThis panel has been compared against the Genomics England PanelApp Intellectual Disability panel, and all discrepancies have been resolved, with reciprocal reviews provided to Genomics England, 11/3/2020.",
                "status": "public",
                "version": "1.760",
                "version_created": "2026-04-26T17:50:23.271073+10:00",
                "relevant_disorders": [
                    "Intellectual disability",
                    "HP:0001249; Neurodevelopmental delay",
                    "HP:0012758"
                ],
                "stats": {
                    "number_of_genes": 2524,
                    "number_of_strs": 10,
                    "number_of_regions": 57
                },
                "types": [
                    {
                        "name": "Genetic Health Queensland",
                        "slug": "genetic-health-queensland",
                        "description": "Panel used by GHQ."
                    },
                    {
                        "name": "Victorian Clinical Genetics Services",
                        "slug": "victorian-clinical-genetics-services",
                        "description": "Panel used by VCGS."
                    },
                    {
                        "name": "Rare Disease",
                        "slug": "rare-disease",
                        "description": "Rare disease panels"
                    },
                    {
                        "name": "Royal Melbourne Hospital",
                        "slug": "royal-melbourne-hospital",
                        "description": "Royal Melbourne Hospital"
                    }
                ],
                "child_panel_ids": []
            },
            "transcript": null
        },
        {
            "gene_data": {
                "alias": [
                    "norrin"
                ],
                "biotype": "protein_coding",
                "hgnc_id": "HGNC:7678",
                "gene_name": "NDP, norrin cystine knot growth factor",
                "omim_gene": [
                    "300658"
                ],
                "alias_name": null,
                "gene_symbol": "NDP",
                "hgnc_symbol": "NDP",
                "hgnc_release": "2017-11-03",
                "ensembl_genes": {
                    "GRch37": {
                        "82": {
                            "location": "X:43808022-43832750",
                            "ensembl_id": "ENSG00000124479"
                        }
                    },
                    "GRch38": {
                        "90": {
                            "location": "X:43948776-43973504",
                            "ensembl_id": "ENSG00000124479"
                        }
                    }
                },
                "hgnc_date_symbol_changed": "2001-06-22"
            },
            "entity_type": "gene",
            "entity_name": "NDP",
            "confidence_level": "3",
            "penetrance": null,
            "mode_of_pathogenicity": "",
            "publications": [],
            "evidence": [
                "Expert Review Green",
                "Genetic Health Queensland"
            ],
            "phenotypes": [
                "Norrie disease MONDO:0010691"
            ],
            "mode_of_inheritance": "X-LINKED: hemizygous mutation in males, biallelic mutations in females",
            "tags": [],
            "panel": {
                "id": 250,
                "hash_id": null,
                "name": "Intellectual disability syndromic and non-syndromic",
                "disease_group": "Neurology and neurodevelopmental disorders",
                "disease_sub_group": "",
                "description": "This panel was created by merging the ID panels used by Genetic Health Queensland and by the Victorian Clinical Genetics Services. Discrepant gene classifications reviewed and resolved by Chirag Patel and Zornitza Stark.\r\n\r\nThis is a consensus panel used by VCGS, GHQ and RMH.\r\n\r\nThis panel has been compared against the Genomics England PanelApp Intellectual Disability panel, and all discrepancies have been resolved, with reciprocal reviews provided to Genomics England, 11/3/2020.",
                "status": "public",
                "version": "1.760",
                "version_created": "2026-04-26T17:50:23.271073+10:00",
                "relevant_disorders": [
                    "Intellectual disability",
                    "HP:0001249; Neurodevelopmental delay",
                    "HP:0012758"
                ],
                "stats": {
                    "number_of_genes": 2524,
                    "number_of_strs": 10,
                    "number_of_regions": 57
                },
                "types": [
                    {
                        "name": "Genetic Health Queensland",
                        "slug": "genetic-health-queensland",
                        "description": "Panel used by GHQ."
                    },
                    {
                        "name": "Victorian Clinical Genetics Services",
                        "slug": "victorian-clinical-genetics-services",
                        "description": "Panel used by VCGS."
                    },
                    {
                        "name": "Rare Disease",
                        "slug": "rare-disease",
                        "description": "Rare disease panels"
                    },
                    {
                        "name": "Royal Melbourne Hospital",
                        "slug": "royal-melbourne-hospital",
                        "description": "Royal Melbourne Hospital"
                    }
                ],
                "child_panel_ids": []
            },
            "transcript": null
        },
        {
            "gene_data": {
                "alias": [
                    "NST1"
                ],
                "biotype": "protein_coding",
                "hgnc_id": "HGNC:7680",
                "gene_name": "N-deacetylase and N-sulfotransferase 1",
                "omim_gene": [
                    "600853"
                ],
                "alias_name": [
                    "[Heparan sulfate]-glucosamine N-sulfotransferase 1",
                    "N-Deacetylase-N-sulfotransferase 1",
                    "heparan sulfate/heparin GlcNAc N-deacetylase/GlcN N-sulfotransferase 1"
                ],
                "gene_symbol": "NDST1",
                "hgnc_symbol": "NDST1",
                "hgnc_release": "2017-11-03",
                "ensembl_genes": {
                    "GRch37": {
                        "82": {
                            "location": "5:149865381-149937773",
                            "ensembl_id": "ENSG00000070614"
                        }
                    },
                    "GRch38": {
                        "90": {
                            "location": "5:150485818-150558211",
                            "ensembl_id": "ENSG00000070614"
                        }
                    }
                },
                "hgnc_date_symbol_changed": "1995-08-10"
            },
            "entity_type": "gene",
            "entity_name": "NDST1",
            "confidence_level": "3",
            "penetrance": null,
            "mode_of_pathogenicity": "",
            "publications": [
                "25125150",
                "21937992",
                "32878022",
                "28211985"
            ],
            "evidence": [
                "Expert Review Green",
                "Genetic Health Queensland"
            ],
            "phenotypes": [
                "Mental retardation, autosomal recessive 46 - MIM#616116"
            ],
            "mode_of_inheritance": "BIALLELIC, autosomal or pseudoautosomal",
            "tags": [],
            "panel": {
                "id": 250,
                "hash_id": null,
                "name": "Intellectual disability syndromic and non-syndromic",
                "disease_group": "Neurology and neurodevelopmental disorders",
                "disease_sub_group": "",
                "description": "This panel was created by merging the ID panels used by Genetic Health Queensland and by the Victorian Clinical Genetics Services. Discrepant gene classifications reviewed and resolved by Chirag Patel and Zornitza Stark.\r\n\r\nThis is a consensus panel used by VCGS, GHQ and RMH.\r\n\r\nThis panel has been compared against the Genomics England PanelApp Intellectual Disability panel, and all discrepancies have been resolved, with reciprocal reviews provided to Genomics England, 11/3/2020.",
                "status": "public",
                "version": "1.760",
                "version_created": "2026-04-26T17:50:23.271073+10:00",
                "relevant_disorders": [
                    "Intellectual disability",
                    "HP:0001249; Neurodevelopmental delay",
                    "HP:0012758"
                ],
                "stats": {
                    "number_of_genes": 2524,
                    "number_of_strs": 10,
                    "number_of_regions": 57
                },
                "types": [
                    {
                        "name": "Genetic Health Queensland",
                        "slug": "genetic-health-queensland",
                        "description": "Panel used by GHQ."
                    },
                    {
                        "name": "Victorian Clinical Genetics Services",
                        "slug": "victorian-clinical-genetics-services",
                        "description": "Panel used by VCGS."
                    },
                    {
                        "name": "Rare Disease",
                        "slug": "rare-disease",
                        "description": "Rare disease panels"
                    },
                    {
                        "name": "Royal Melbourne Hospital",
                        "slug": "royal-melbourne-hospital",
                        "description": "Royal Melbourne Hospital"
                    }
                ],
                "child_panel_ids": []
            },
            "transcript": null
        },
        {
            "gene_data": {
                "alias": [
                    "MWFE",
                    "CI-MWFE"
                ],
                "biotype": "protein_coding",
                "hgnc_id": "HGNC:7683",
                "gene_name": "NADH:ubiquinone oxidoreductase subunit A1",
                "omim_gene": [
                    "300078"
                ],
                "alias_name": [
                    "NADH:ubiquinone oxidoreductase (complex 1)",
                    "type I dehydrogenase",
                    "NADH dehydrogenase (ubiquinone) 1 alpha subcomplex, 1 (7.5kD, MWFE)",
                    "complex I MWFE subunit"
                ],
                "gene_symbol": "NDUFA1",
                "hgnc_symbol": "NDUFA1",
                "hgnc_release": "2017-11-03",
                "ensembl_genes": {
                    "GRch37": {
                        "82": {
                            "location": "X:119005450-119010625",
                            "ensembl_id": "ENSG00000125356"
                        }
                    },
                    "GRch38": {
                        "90": {
                            "location": "X:119871487-119876662",
                            "ensembl_id": "ENSG00000125356"
                        }
                    }
                },
                "hgnc_date_symbol_changed": "1996-08-16"
            },
            "entity_type": "gene",
            "entity_name": "NDUFA1",
            "confidence_level": "3",
            "penetrance": null,
            "mode_of_pathogenicity": "",
            "publications": [
                "29506883",
                "19185523",
                "17262856",
                "21596602"
            ],
            "evidence": [
                "Expert Review Green",
                "Genetic Health Queensland"
            ],
            "phenotypes": [
                "Mitochondrial complex I deficiency, nuclear type 12 MIM#301020"
            ],
            "mode_of_inheritance": "X-LINKED: hemizygous mutation in males, biallelic mutations in females",
            "tags": [],
            "panel": {
                "id": 250,
                "hash_id": null,
                "name": "Intellectual disability syndromic and non-syndromic",
                "disease_group": "Neurology and neurodevelopmental disorders",
                "disease_sub_group": "",
                "description": "This panel was created by merging the ID panels used by Genetic Health Queensland and by the Victorian Clinical Genetics Services. Discrepant gene classifications reviewed and resolved by Chirag Patel and Zornitza Stark.\r\n\r\nThis is a consensus panel used by VCGS, GHQ and RMH.\r\n\r\nThis panel has been compared against the Genomics England PanelApp Intellectual Disability panel, and all discrepancies have been resolved, with reciprocal reviews provided to Genomics England, 11/3/2020.",
                "status": "public",
                "version": "1.760",
                "version_created": "2026-04-26T17:50:23.271073+10:00",
                "relevant_disorders": [
                    "Intellectual disability",
                    "HP:0001249; Neurodevelopmental delay",
                    "HP:0012758"
                ],
                "stats": {
                    "number_of_genes": 2524,
                    "number_of_strs": 10,
                    "number_of_regions": 57
                },
                "types": [
                    {
                        "name": "Genetic Health Queensland",
                        "slug": "genetic-health-queensland",
                        "description": "Panel used by GHQ."
                    },
                    {
                        "name": "Victorian Clinical Genetics Services",
                        "slug": "victorian-clinical-genetics-services",
                        "description": "Panel used by VCGS."
                    },
                    {
                        "name": "Rare Disease",
                        "slug": "rare-disease",
                        "description": "Rare disease panels"
                    },
                    {
                        "name": "Royal Melbourne Hospital",
                        "slug": "royal-melbourne-hospital",
                        "description": "Royal Melbourne Hospital"
                    }
                ],
                "child_panel_ids": []
            },
            "transcript": null
        },
        {
            "gene_data": {
                "alias": [
                    "CI-42k"
                ],
                "biotype": "protein_coding",
                "hgnc_id": "HGNC:7684",
                "gene_name": "NADH:ubiquinone oxidoreductase subunit A10",
                "omim_gene": [
                    "603835"
                ],
                "alias_name": [
                    "complex I 42kDa subunit"
                ],
                "gene_symbol": "NDUFA10",
                "hgnc_symbol": "NDUFA10",
                "hgnc_release": "2017-11-03",
                "ensembl_genes": {
                    "GRch37": {
                        "82": {
                            "location": "2:240831867-240964819",
                            "ensembl_id": "ENSG00000130414"
                        }
                    },
                    "GRch38": {
                        "90": {
                            "location": "2:239892450-240025402",
                            "ensembl_id": "ENSG00000130414"
                        }
                    }
                },
                "hgnc_date_symbol_changed": "1997-12-17"
            },
            "entity_type": "gene",
            "entity_name": "NDUFA10",
            "confidence_level": "2",
            "penetrance": null,
            "mode_of_pathogenicity": "",
            "publications": [
                "21150889",
                "26741492"
            ],
            "evidence": [
                "Expert Review Amber",
                "Genetic Health Queensland"
            ],
            "phenotypes": [
                "Mitochondrial complex I deficiency, nuclear type 22, MIM#618243"
            ],
            "mode_of_inheritance": "BIALLELIC, autosomal or pseudoautosomal",
            "tags": [],
            "panel": {
                "id": 250,
                "hash_id": null,
                "name": "Intellectual disability syndromic and non-syndromic",
                "disease_group": "Neurology and neurodevelopmental disorders",
                "disease_sub_group": "",
                "description": "This panel was created by merging the ID panels used by Genetic Health Queensland and by the Victorian Clinical Genetics Services. Discrepant gene classifications reviewed and resolved by Chirag Patel and Zornitza Stark.\r\n\r\nThis is a consensus panel used by VCGS, GHQ and RMH.\r\n\r\nThis panel has been compared against the Genomics England PanelApp Intellectual Disability panel, and all discrepancies have been resolved, with reciprocal reviews provided to Genomics England, 11/3/2020.",
                "status": "public",
                "version": "1.760",
                "version_created": "2026-04-26T17:50:23.271073+10:00",
                "relevant_disorders": [
                    "Intellectual disability",
                    "HP:0001249; Neurodevelopmental delay",
                    "HP:0012758"
                ],
                "stats": {
                    "number_of_genes": 2524,
                    "number_of_strs": 10,
                    "number_of_regions": 57
                },
                "types": [
                    {
                        "name": "Genetic Health Queensland",
                        "slug": "genetic-health-queensland",
                        "description": "Panel used by GHQ."
                    },
                    {
                        "name": "Victorian Clinical Genetics Services",
                        "slug": "victorian-clinical-genetics-services",
                        "description": "Panel used by VCGS."
                    },
                    {
                        "name": "Rare Disease",
                        "slug": "rare-disease",
                        "description": "Rare disease panels"
                    },
                    {
                        "name": "Royal Melbourne Hospital",
                        "slug": "royal-melbourne-hospital",
                        "description": "Royal Melbourne Hospital"
                    }
                ],
                "child_panel_ids": []
            },
            "transcript": null
        },
        {
            "gene_data": {
                "alias": [
                    "B14.7"
                ],
                "biotype": "protein_coding",
                "hgnc_id": "HGNC:20371",
                "gene_name": "NADH:ubiquinone oxidoreductase subunit A11",
                "omim_gene": [
                    "612638"
                ],
                "alias_name": [
                    "complex I B14.7 subunit"
                ],
                "gene_symbol": "NDUFA11",
                "hgnc_symbol": "NDUFA11",
                "hgnc_release": "2017-11-03",
                "ensembl_genes": {
                    "GRch37": {
                        "82": {
                            "location": "19:5891287-5904017",
                            "ensembl_id": "ENSG00000174886"
                        }
                    },
                    "GRch38": {
                        "90": {
                            "location": "19:5891276-5904006",
                            "ensembl_id": "ENSG00000174886"
                        }
                    }
                },
                "hgnc_date_symbol_changed": "2003-12-03"
            },
            "entity_type": "gene",
            "entity_name": "NDUFA11",
            "confidence_level": "2",
            "penetrance": null,
            "mode_of_pathogenicity": "",
            "publications": [
                "18306244",
                "31074871"
            ],
            "evidence": [
                "Expert Review Amber",
                "Genetic Health Queensland"
            ],
            "phenotypes": [
                "Mitochondrial complex I deficiency, nuclear type 14, MIM#618236"
            ],
            "mode_of_inheritance": "BIALLELIC, autosomal or pseudoautosomal",
            "tags": [],
            "panel": {
                "id": 250,
                "hash_id": null,
                "name": "Intellectual disability syndromic and non-syndromic",
                "disease_group": "Neurology and neurodevelopmental disorders",
                "disease_sub_group": "",
                "description": "This panel was created by merging the ID panels used by Genetic Health Queensland and by the Victorian Clinical Genetics Services. Discrepant gene classifications reviewed and resolved by Chirag Patel and Zornitza Stark.\r\n\r\nThis is a consensus panel used by VCGS, GHQ and RMH.\r\n\r\nThis panel has been compared against the Genomics England PanelApp Intellectual Disability panel, and all discrepancies have been resolved, with reciprocal reviews provided to Genomics England, 11/3/2020.",
                "status": "public",
                "version": "1.760",
                "version_created": "2026-04-26T17:50:23.271073+10:00",
                "relevant_disorders": [
                    "Intellectual disability",
                    "HP:0001249; Neurodevelopmental delay",
                    "HP:0012758"
                ],
                "stats": {
                    "number_of_genes": 2524,
                    "number_of_strs": 10,
                    "number_of_regions": 57
                },
                "types": [
                    {
                        "name": "Genetic Health Queensland",
                        "slug": "genetic-health-queensland",
                        "description": "Panel used by GHQ."
                    },
                    {
                        "name": "Victorian Clinical Genetics Services",
                        "slug": "victorian-clinical-genetics-services",
                        "description": "Panel used by VCGS."
                    },
                    {
                        "name": "Rare Disease",
                        "slug": "rare-disease",
                        "description": "Rare disease panels"
                    },
                    {
                        "name": "Royal Melbourne Hospital",
                        "slug": "royal-melbourne-hospital",
                        "description": "Royal Melbourne Hospital"
                    }
                ],
                "child_panel_ids": []
            },
            "transcript": null
        },
        {
            "gene_data": {
                "alias": [
                    "B8"
                ],
                "biotype": "protein_coding",
                "hgnc_id": "HGNC:7685",
                "gene_name": "NADH:ubiquinone oxidoreductase subunit A2",
                "omim_gene": [
                    "602137"
                ],
                "alias_name": [
                    "complex I B8 subunit"
                ],
                "gene_symbol": "NDUFA2",
                "hgnc_symbol": "NDUFA2",
                "hgnc_release": "2017-11-03",
                "ensembl_genes": {
                    "GRch37": {
                        "82": {
                            "location": "5:140018325-140027370",
                            "ensembl_id": "ENSG00000131495"
                        }
                    },
                    "GRch38": {
                        "90": {
                            "location": "5:140638740-140647785",
                            "ensembl_id": "ENSG00000131495"
                        }
                    }
                },
                "hgnc_date_symbol_changed": "1996-08-30"
            },
            "entity_type": "gene",
            "entity_name": "NDUFA2",
            "confidence_level": "3",
            "penetrance": null,
            "mode_of_pathogenicity": "",
            "publications": [
                "18513682",
                "28857146"
            ],
            "evidence": [
                "Expert Review Green",
                "Genetic Health Queensland"
            ],
            "phenotypes": [
                "Mitochondrial complex I deficiency, nuclear type 13, MIM#618235"
            ],
            "mode_of_inheritance": "BIALLELIC, autosomal or pseudoautosomal",
            "tags": [],
            "panel": {
                "id": 250,
                "hash_id": null,
                "name": "Intellectual disability syndromic and non-syndromic",
                "disease_group": "Neurology and neurodevelopmental disorders",
                "disease_sub_group": "",
                "description": "This panel was created by merging the ID panels used by Genetic Health Queensland and by the Victorian Clinical Genetics Services. Discrepant gene classifications reviewed and resolved by Chirag Patel and Zornitza Stark.\r\n\r\nThis is a consensus panel used by VCGS, GHQ and RMH.\r\n\r\nThis panel has been compared against the Genomics England PanelApp Intellectual Disability panel, and all discrepancies have been resolved, with reciprocal reviews provided to Genomics England, 11/3/2020.",
                "status": "public",
                "version": "1.760",
                "version_created": "2026-04-26T17:50:23.271073+10:00",
                "relevant_disorders": [
                    "Intellectual disability",
                    "HP:0001249; Neurodevelopmental delay",
                    "HP:0012758"
                ],
                "stats": {
                    "number_of_genes": 2524,
                    "number_of_strs": 10,
                    "number_of_regions": 57
                },
                "types": [
                    {
                        "name": "Genetic Health Queensland",
                        "slug": "genetic-health-queensland",
                        "description": "Panel used by GHQ."
                    },
                    {
                        "name": "Victorian Clinical Genetics Services",
                        "slug": "victorian-clinical-genetics-services",
                        "description": "Panel used by VCGS."
                    },
                    {
                        "name": "Rare Disease",
                        "slug": "rare-disease",
                        "description": "Rare disease panels"
                    },
                    {
                        "name": "Royal Melbourne Hospital",
                        "slug": "royal-melbourne-hospital",
                        "description": "Royal Melbourne Hospital"
                    }
                ],
                "child_panel_ids": []
            },
            "transcript": null
        },
        {
            "gene_data": {
                "alias": [
                    "SDR22E1",
                    "CI-39k"
                ],
                "biotype": "protein_coding",
                "hgnc_id": "HGNC:7693",
                "gene_name": "NADH:ubiquinone oxidoreductase subunit A9",
                "omim_gene": [
                    "603834"
                ],
                "alias_name": [
                    "short chain dehydrogenase/reductase family 22E, member 1",
                    "complex I 39kDa subunit"
                ],
                "gene_symbol": "NDUFA9",
                "hgnc_symbol": "NDUFA9",
                "hgnc_release": "2017-11-03",
                "ensembl_genes": {
                    "GRch37": {
                        "82": {
                            "location": "12:4758261-4798454",
                            "ensembl_id": "ENSG00000139180"
                        }
                    },
                    "GRch38": {
                        "90": {
                            "location": "12:4649095-4694317",
                            "ensembl_id": "ENSG00000139180"
                        }
                    }
                },
                "hgnc_date_symbol_changed": "1997-12-17"
            },
            "entity_type": "gene",
            "entity_name": "NDUFA9",
            "confidence_level": "2",
            "penetrance": null,
            "mode_of_pathogenicity": "",
            "publications": [
                "28671271",
                "22114105"
            ],
            "evidence": [
                "Expert Review Amber",
                "Genetic Health Queensland"
            ],
            "phenotypes": [
                "Mitochondrial complex I deficiency, nuclear type 26, MIM#618247"
            ],
            "mode_of_inheritance": "BIALLELIC, autosomal or pseudoautosomal",
            "tags": [],
            "panel": {
                "id": 250,
                "hash_id": null,
                "name": "Intellectual disability syndromic and non-syndromic",
                "disease_group": "Neurology and neurodevelopmental disorders",
                "disease_sub_group": "",
                "description": "This panel was created by merging the ID panels used by Genetic Health Queensland and by the Victorian Clinical Genetics Services. Discrepant gene classifications reviewed and resolved by Chirag Patel and Zornitza Stark.\r\n\r\nThis is a consensus panel used by VCGS, GHQ and RMH.\r\n\r\nThis panel has been compared against the Genomics England PanelApp Intellectual Disability panel, and all discrepancies have been resolved, with reciprocal reviews provided to Genomics England, 11/3/2020.",
                "status": "public",
                "version": "1.760",
                "version_created": "2026-04-26T17:50:23.271073+10:00",
                "relevant_disorders": [
                    "Intellectual disability",
                    "HP:0001249; Neurodevelopmental delay",
                    "HP:0012758"
                ],
                "stats": {
                    "number_of_genes": 2524,
                    "number_of_strs": 10,
                    "number_of_regions": 57
                },
                "types": [
                    {
                        "name": "Genetic Health Queensland",
                        "slug": "genetic-health-queensland",
                        "description": "Panel used by GHQ."
                    },
                    {
                        "name": "Victorian Clinical Genetics Services",
                        "slug": "victorian-clinical-genetics-services",
                        "description": "Panel used by VCGS."
                    },
                    {
                        "name": "Rare Disease",
                        "slug": "rare-disease",
                        "description": "Rare disease panels"
                    },
                    {
                        "name": "Royal Melbourne Hospital",
                        "slug": "royal-melbourne-hospital",
                        "description": "Royal Melbourne Hospital"
                    }
                ],
                "child_panel_ids": []
            },
            "transcript": null
        },
        {
            "gene_data": {
                "alias": [
                    "CIA30",
                    "CGI-65"
                ],
                "biotype": "protein_coding",
                "hgnc_id": "HGNC:18828",
                "gene_name": "NADH:ubiquinone oxidoreductase complex assembly factor 1",
                "omim_gene": [
                    "606934"
                ],
                "alias_name": null,
                "gene_symbol": "NDUFAF1",
                "hgnc_symbol": "NDUFAF1",
                "hgnc_release": "2017-11-03",
                "ensembl_genes": {
                    "GRch37": {
                        "82": {
                            "location": "15:41679551-41694717",
                            "ensembl_id": "ENSG00000137806"
                        }
                    },
                    "GRch38": {
                        "90": {
                            "location": "15:41387349-41402519",
                            "ensembl_id": "ENSG00000137806"
                        }
                    }
                },
                "hgnc_date_symbol_changed": "2004-02-02"
            },
            "entity_type": "gene",
            "entity_name": "NDUFAF1",
            "confidence_level": "3",
            "penetrance": null,
            "mode_of_pathogenicity": "",
            "publications": [
                "17557076",
                "21931170",
                "24963768"
            ],
            "evidence": [
                "Expert Review Green",
                "Genetic Health Queensland"
            ],
            "phenotypes": [
                "Mitochondrial complex I deficiency, nuclear type 11, MIM#618234"
            ],
            "mode_of_inheritance": "BIALLELIC, autosomal or pseudoautosomal",
            "tags": [],
            "panel": {
                "id": 250,
                "hash_id": null,
                "name": "Intellectual disability syndromic and non-syndromic",
                "disease_group": "Neurology and neurodevelopmental disorders",
                "disease_sub_group": "",
                "description": "This panel was created by merging the ID panels used by Genetic Health Queensland and by the Victorian Clinical Genetics Services. Discrepant gene classifications reviewed and resolved by Chirag Patel and Zornitza Stark.\r\n\r\nThis is a consensus panel used by VCGS, GHQ and RMH.\r\n\r\nThis panel has been compared against the Genomics England PanelApp Intellectual Disability panel, and all discrepancies have been resolved, with reciprocal reviews provided to Genomics England, 11/3/2020.",
                "status": "public",
                "version": "1.760",
                "version_created": "2026-04-26T17:50:23.271073+10:00",
                "relevant_disorders": [
                    "Intellectual disability",
                    "HP:0001249; Neurodevelopmental delay",
                    "HP:0012758"
                ],
                "stats": {
                    "number_of_genes": 2524,
                    "number_of_strs": 10,
                    "number_of_regions": 57
                },
                "types": [
                    {
                        "name": "Genetic Health Queensland",
                        "slug": "genetic-health-queensland",
                        "description": "Panel used by GHQ."
                    },
                    {
                        "name": "Victorian Clinical Genetics Services",
                        "slug": "victorian-clinical-genetics-services",
                        "description": "Panel used by VCGS."
                    },
                    {
                        "name": "Rare Disease",
                        "slug": "rare-disease",
                        "description": "Rare disease panels"
                    },
                    {
                        "name": "Royal Melbourne Hospital",
                        "slug": "royal-melbourne-hospital",
                        "description": "Royal Melbourne Hospital"
                    }
                ],
                "child_panel_ids": []
            },
            "transcript": null
        },
        {
            "gene_data": {
                "alias": [
                    "B17.2L",
                    "MMTN",
                    "mimitin"
                ],
                "biotype": "protein_coding",
                "hgnc_id": "HGNC:28086",
                "gene_name": "NADH:ubiquinone oxidoreductase complex assembly factor 2",
                "omim_gene": [
                    "609653"
                ],
                "alias_name": [
                    "Myc-induced mitochondrial protein"
                ],
                "gene_symbol": "NDUFAF2",
                "hgnc_symbol": "NDUFAF2",
                "hgnc_release": "2017-11-03",
                "ensembl_genes": {
                    "GRch37": {
                        "82": {
                            "location": "5:60240956-60448853",
                            "ensembl_id": "ENSG00000164182"
                        }
                    },
                    "GRch38": {
                        "90": {
                            "location": "5:60945129-61153037",
                            "ensembl_id": "ENSG00000164182"
                        }
                    }
                },
                "hgnc_date_symbol_changed": "2008-02-15"
            },
            "entity_type": "gene",
            "entity_name": "NDUFAF2",
            "confidence_level": "2",
            "penetrance": null,
            "mode_of_pathogenicity": "",
            "publications": [
                "18180188",
                "20571988",
                "19384974",
                "16200211"
            ],
            "evidence": [
                "Expert Review Amber",
                "Genetic Health Queensland"
            ],
            "phenotypes": [
                "Mitochondrial complex I deficiency, nuclear type 10, MIM#618233"
            ],
            "mode_of_inheritance": "BIALLELIC, autosomal or pseudoautosomal",
            "tags": [],
            "panel": {
                "id": 250,
                "hash_id": null,
                "name": "Intellectual disability syndromic and non-syndromic",
                "disease_group": "Neurology and neurodevelopmental disorders",
                "disease_sub_group": "",
                "description": "This panel was created by merging the ID panels used by Genetic Health Queensland and by the Victorian Clinical Genetics Services. Discrepant gene classifications reviewed and resolved by Chirag Patel and Zornitza Stark.\r\n\r\nThis is a consensus panel used by VCGS, GHQ and RMH.\r\n\r\nThis panel has been compared against the Genomics England PanelApp Intellectual Disability panel, and all discrepancies have been resolved, with reciprocal reviews provided to Genomics England, 11/3/2020.",
                "status": "public",
                "version": "1.760",
                "version_created": "2026-04-26T17:50:23.271073+10:00",
                "relevant_disorders": [
                    "Intellectual disability",
                    "HP:0001249; Neurodevelopmental delay",
                    "HP:0012758"
                ],
                "stats": {
                    "number_of_genes": 2524,
                    "number_of_strs": 10,
                    "number_of_regions": 57
                },
                "types": [
                    {
                        "name": "Genetic Health Queensland",
                        "slug": "genetic-health-queensland",
                        "description": "Panel used by GHQ."
                    },
                    {
                        "name": "Victorian Clinical Genetics Services",
                        "slug": "victorian-clinical-genetics-services",
                        "description": "Panel used by VCGS."
                    },
                    {
                        "name": "Rare Disease",
                        "slug": "rare-disease",
                        "description": "Rare disease panels"
                    },
                    {
                        "name": "Royal Melbourne Hospital",
                        "slug": "royal-melbourne-hospital",
                        "description": "Royal Melbourne Hospital"
                    }
                ],
                "child_panel_ids": []
            },
            "transcript": null
        },
        {
            "gene_data": {
                "alias": [
                    "MGC10527",
                    "DKFZP564J0123",
                    "E3-3",
                    "2P1"
                ],
                "biotype": "protein_coding",
                "hgnc_id": "HGNC:29918",
                "gene_name": "NADH:ubiquinone oxidoreductase complex assembly factor 3",
                "omim_gene": [
                    "612911"
                ],
                "alias_name": null,
                "gene_symbol": "NDUFAF3",
                "hgnc_symbol": "NDUFAF3",
                "hgnc_release": "2017-11-03",
                "ensembl_genes": {
                    "GRch37": {
                        "82": {
                            "location": "3:49057892-49060928",
                            "ensembl_id": "ENSG00000178057"
                        }
                    },
                    "GRch38": {
                        "90": {
                            "location": "3:49020459-49023495",
                            "ensembl_id": "ENSG00000178057"
                        }
                    }
                },
                "hgnc_date_symbol_changed": "2009-03-18"
            },
            "entity_type": "gene",
            "entity_name": "NDUFAF3",
            "confidence_level": "2",
            "penetrance": null,
            "mode_of_pathogenicity": "",
            "publications": [
                "19463981"
            ],
            "evidence": [
                "Expert Review Amber",
                "Genetic Health Queensland"
            ],
            "phenotypes": [
                "Mitochondrial complex I deficiency, nuclear type 18, MIM#618240"
            ],
            "mode_of_inheritance": "BIALLELIC, autosomal or pseudoautosomal",
            "tags": [],
            "panel": {
                "id": 250,
                "hash_id": null,
                "name": "Intellectual disability syndromic and non-syndromic",
                "disease_group": "Neurology and neurodevelopmental disorders",
                "disease_sub_group": "",
                "description": "This panel was created by merging the ID panels used by Genetic Health Queensland and by the Victorian Clinical Genetics Services. Discrepant gene classifications reviewed and resolved by Chirag Patel and Zornitza Stark.\r\n\r\nThis is a consensus panel used by VCGS, GHQ and RMH.\r\n\r\nThis panel has been compared against the Genomics England PanelApp Intellectual Disability panel, and all discrepancies have been resolved, with reciprocal reviews provided to Genomics England, 11/3/2020.",
                "status": "public",
                "version": "1.760",
                "version_created": "2026-04-26T17:50:23.271073+10:00",
                "relevant_disorders": [
                    "Intellectual disability",
                    "HP:0001249; Neurodevelopmental delay",
                    "HP:0012758"
                ],
                "stats": {
                    "number_of_genes": 2524,
                    "number_of_strs": 10,
                    "number_of_regions": 57
                },
                "types": [
                    {
                        "name": "Genetic Health Queensland",
                        "slug": "genetic-health-queensland",
                        "description": "Panel used by GHQ."
                    },
                    {
                        "name": "Victorian Clinical Genetics Services",
                        "slug": "victorian-clinical-genetics-services",
                        "description": "Panel used by VCGS."
                    },
                    {
                        "name": "Rare Disease",
                        "slug": "rare-disease",
                        "description": "Rare disease panels"
                    },
                    {
                        "name": "Royal Melbourne Hospital",
                        "slug": "royal-melbourne-hospital",
                        "description": "Royal Melbourne Hospital"
                    }
                ],
                "child_panel_ids": []
            },
            "transcript": null
        },
        {
            "gene_data": {
                "alias": [
                    "HSPC125",
                    "bA22L21.1",
                    "My013",
                    "HRPAP20"
                ],
                "biotype": "protein_coding",
                "hgnc_id": "HGNC:21034",
                "gene_name": "NADH:ubiquinone oxidoreductase complex assembly factor 4",
                "omim_gene": [
                    "611776"
                ],
                "alias_name": null,
                "gene_symbol": "NDUFAF4",
                "hgnc_symbol": "NDUFAF4",
                "hgnc_release": "2017-11-03",
                "ensembl_genes": {
                    "GRch37": {
                        "82": {
                            "location": "6:97337189-97345757",
                            "ensembl_id": "ENSG00000123545"
                        }
                    },
                    "GRch38": {
                        "90": {
                            "location": "6:96889313-96897881",
                            "ensembl_id": "ENSG00000123545"
                        }
                    }
                },
                "hgnc_date_symbol_changed": "2009-03-18"
            },
            "entity_type": "gene",
            "entity_name": "NDUFAF4",
            "confidence_level": "2",
            "penetrance": null,
            "mode_of_pathogenicity": "",
            "publications": [
                "18179882",
                "28853723"
            ],
            "evidence": [
                "Expert Review Amber",
                "Genetic Health Queensland"
            ],
            "phenotypes": [
                "Mitochondrial complex I deficiency, nuclear type 15, MIM#618237"
            ],
            "mode_of_inheritance": "BIALLELIC, autosomal or pseudoautosomal",
            "tags": [],
            "panel": {
                "id": 250,
                "hash_id": null,
                "name": "Intellectual disability syndromic and non-syndromic",
                "disease_group": "Neurology and neurodevelopmental disorders",
                "disease_sub_group": "",
                "description": "This panel was created by merging the ID panels used by Genetic Health Queensland and by the Victorian Clinical Genetics Services. Discrepant gene classifications reviewed and resolved by Chirag Patel and Zornitza Stark.\r\n\r\nThis is a consensus panel used by VCGS, GHQ and RMH.\r\n\r\nThis panel has been compared against the Genomics England PanelApp Intellectual Disability panel, and all discrepancies have been resolved, with reciprocal reviews provided to Genomics England, 11/3/2020.",
                "status": "public",
                "version": "1.760",
                "version_created": "2026-04-26T17:50:23.271073+10:00",
                "relevant_disorders": [
                    "Intellectual disability",
                    "HP:0001249; Neurodevelopmental delay",
                    "HP:0012758"
                ],
                "stats": {
                    "number_of_genes": 2524,
                    "number_of_strs": 10,
                    "number_of_regions": 57
                },
                "types": [
                    {
                        "name": "Genetic Health Queensland",
                        "slug": "genetic-health-queensland",
                        "description": "Panel used by GHQ."
                    },
                    {
                        "name": "Victorian Clinical Genetics Services",
                        "slug": "victorian-clinical-genetics-services",
                        "description": "Panel used by VCGS."
                    },
                    {
                        "name": "Rare Disease",
                        "slug": "rare-disease",
                        "description": "Rare disease panels"
                    },
                    {
                        "name": "Royal Melbourne Hospital",
                        "slug": "royal-melbourne-hospital",
                        "description": "Royal Melbourne Hospital"
                    }
                ],
                "child_panel_ids": []
            },
            "transcript": null
        },
        {
            "gene_data": {
                "alias": [
                    "dJ842G6.1"
                ],
                "biotype": "protein_coding",
                "hgnc_id": "HGNC:15899",
                "gene_name": "NADH:ubiquinone oxidoreductase complex assembly factor 5",
                "omim_gene": [
                    "612360"
                ],
                "alias_name": null,
                "gene_symbol": "NDUFAF5",
                "hgnc_symbol": "NDUFAF5",
                "hgnc_release": "2017-11-03",
                "ensembl_genes": {
                    "GRch37": {
                        "82": {
                            "location": "20:13765596-13799067",
                            "ensembl_id": "ENSG00000101247"
                        }
                    },
                    "GRch38": {
                        "90": {
                            "location": "20:13784950-13821582",
                            "ensembl_id": "ENSG00000101247"
                        }
                    }
                },
                "hgnc_date_symbol_changed": "2012-05-08"
            },
            "entity_type": "gene",
            "entity_name": "NDUFAF5",
            "confidence_level": "2",
            "penetrance": null,
            "mode_of_pathogenicity": "",
            "publications": [
                "19542079",
                "21607760",
                "18940309"
            ],
            "evidence": [
                "Expert Review Amber",
                "Genetic Health Queensland"
            ],
            "phenotypes": [
                "Mitochondrial complex I deficiency, nuclear type 16, MIM# 618238"
            ],
            "mode_of_inheritance": "BIALLELIC, autosomal or pseudoautosomal",
            "tags": [],
            "panel": {
                "id": 250,
                "hash_id": null,
                "name": "Intellectual disability syndromic and non-syndromic",
                "disease_group": "Neurology and neurodevelopmental disorders",
                "disease_sub_group": "",
                "description": "This panel was created by merging the ID panels used by Genetic Health Queensland and by the Victorian Clinical Genetics Services. Discrepant gene classifications reviewed and resolved by Chirag Patel and Zornitza Stark.\r\n\r\nThis is a consensus panel used by VCGS, GHQ and RMH.\r\n\r\nThis panel has been compared against the Genomics England PanelApp Intellectual Disability panel, and all discrepancies have been resolved, with reciprocal reviews provided to Genomics England, 11/3/2020.",
                "status": "public",
                "version": "1.760",
                "version_created": "2026-04-26T17:50:23.271073+10:00",
                "relevant_disorders": [
                    "Intellectual disability",
                    "HP:0001249; Neurodevelopmental delay",
                    "HP:0012758"
                ],
                "stats": {
                    "number_of_genes": 2524,
                    "number_of_strs": 10,
                    "number_of_regions": 57
                },
                "types": [
                    {
                        "name": "Genetic Health Queensland",
                        "slug": "genetic-health-queensland",
                        "description": "Panel used by GHQ."
                    },
                    {
                        "name": "Victorian Clinical Genetics Services",
                        "slug": "victorian-clinical-genetics-services",
                        "description": "Panel used by VCGS."
                    },
                    {
                        "name": "Rare Disease",
                        "slug": "rare-disease",
                        "description": "Rare disease panels"
                    },
                    {
                        "name": "Royal Melbourne Hospital",
                        "slug": "royal-melbourne-hospital",
                        "description": "Royal Melbourne Hospital"
                    }
                ],
                "child_panel_ids": []
            },
            "transcript": null
        },
        {
            "gene_data": {
                "alias": [
                    "MGC40214"
                ],
                "biotype": "protein_coding",
                "hgnc_id": "HGNC:28625",
                "gene_name": "NADH:ubiquinone oxidoreductase complex assembly factor 6",
                "omim_gene": [
                    "612392"
                ],
                "alias_name": null,
                "gene_symbol": "NDUFAF6",
                "hgnc_symbol": "NDUFAF6",
                "hgnc_release": "2017-11-03",
                "ensembl_genes": {
                    "GRch37": {
                        "82": {
                            "location": "8:95907995-96128683",
                            "ensembl_id": "ENSG00000156170"
                        }
                    },
                    "GRch38": {
                        "90": {
                            "location": "8:94895767-95116455",
                            "ensembl_id": "ENSG00000156170"
                        }
                    }
                },
                "hgnc_date_symbol_changed": "2012-05-08"
            },
            "entity_type": "gene",
            "entity_name": "NDUFAF6",
            "confidence_level": "2",
            "penetrance": null,
            "mode_of_pathogenicity": "",
            "publications": [
                "26741492",
                "18614015"
            ],
            "evidence": [
                "Expert Review Amber",
                "Genetic Health Queensland"
            ],
            "phenotypes": [
                "Mitochondrial complex I deficiency, nuclear type 17, MIM#618239"
            ],
            "mode_of_inheritance": "BIALLELIC, autosomal or pseudoautosomal",
            "tags": [],
            "panel": {
                "id": 250,
                "hash_id": null,
                "name": "Intellectual disability syndromic and non-syndromic",
                "disease_group": "Neurology and neurodevelopmental disorders",
                "disease_sub_group": "",
                "description": "This panel was created by merging the ID panels used by Genetic Health Queensland and by the Victorian Clinical Genetics Services. Discrepant gene classifications reviewed and resolved by Chirag Patel and Zornitza Stark.\r\n\r\nThis is a consensus panel used by VCGS, GHQ and RMH.\r\n\r\nThis panel has been compared against the Genomics England PanelApp Intellectual Disability panel, and all discrepancies have been resolved, with reciprocal reviews provided to Genomics England, 11/3/2020.",
                "status": "public",
                "version": "1.760",
                "version_created": "2026-04-26T17:50:23.271073+10:00",
                "relevant_disorders": [
                    "Intellectual disability",
                    "HP:0001249; Neurodevelopmental delay",
                    "HP:0012758"
                ],
                "stats": {
                    "number_of_genes": 2524,
                    "number_of_strs": 10,
                    "number_of_regions": 57
                },
                "types": [
                    {
                        "name": "Genetic Health Queensland",
                        "slug": "genetic-health-queensland",
                        "description": "Panel used by GHQ."
                    },
                    {
                        "name": "Victorian Clinical Genetics Services",
                        "slug": "victorian-clinical-genetics-services",
                        "description": "Panel used by VCGS."
                    },
                    {
                        "name": "Rare Disease",
                        "slug": "rare-disease",
                        "description": "Rare disease panels"
                    },
                    {
                        "name": "Royal Melbourne Hospital",
                        "slug": "royal-melbourne-hospital",
                        "description": "Royal Melbourne Hospital"
                    }
                ],
                "child_panel_ids": []
            },
            "transcript": null
        },
        {
            "gene_data": {
                "alias": [
                    "B12"
                ],
                "biotype": "protein_coding",
                "hgnc_id": "HGNC:7698",
                "gene_name": "NADH:ubiquinone oxidoreductase subunit B3",
                "omim_gene": [
                    "603839"
                ],
                "alias_name": [
                    "complex I B12 subunit"
                ],
                "gene_symbol": "NDUFB3",
                "hgnc_symbol": "NDUFB3",
                "hgnc_release": "2017-11-03",
                "ensembl_genes": {
                    "GRch37": {
                        "82": {
                            "location": "2:201936156-201950473",
                            "ensembl_id": "ENSG00000119013"
                        }
                    },
                    "GRch38": {
                        "90": {
                            "location": "2:201071433-201085750",
                            "ensembl_id": "ENSG00000119013"
                        }
                    }
                },
                "hgnc_date_symbol_changed": "1997-12-17"
            },
            "entity_type": "gene",
            "entity_name": "NDUFB3",
            "confidence_level": "2",
            "penetrance": null,
            "mode_of_pathogenicity": "",
            "publications": [
                "22277967",
                "22499348",
                "27091925"
            ],
            "evidence": [
                "Expert Review Amber",
                "Genetic Health Queensland"
            ],
            "phenotypes": [
                "Mitochondrial complex I deficiency, nuclear type 25, MIM#618246"
            ],
            "mode_of_inheritance": "BIALLELIC, autosomal or pseudoautosomal",
            "tags": [],
            "panel": {
                "id": 250,
                "hash_id": null,
                "name": "Intellectual disability syndromic and non-syndromic",
                "disease_group": "Neurology and neurodevelopmental disorders",
                "disease_sub_group": "",
                "description": "This panel was created by merging the ID panels used by Genetic Health Queensland and by the Victorian Clinical Genetics Services. Discrepant gene classifications reviewed and resolved by Chirag Patel and Zornitza Stark.\r\n\r\nThis is a consensus panel used by VCGS, GHQ and RMH.\r\n\r\nThis panel has been compared against the Genomics England PanelApp Intellectual Disability panel, and all discrepancies have been resolved, with reciprocal reviews provided to Genomics England, 11/3/2020.",
                "status": "public",
                "version": "1.760",
                "version_created": "2026-04-26T17:50:23.271073+10:00",
                "relevant_disorders": [
                    "Intellectual disability",
                    "HP:0001249; Neurodevelopmental delay",
                    "HP:0012758"
                ],
                "stats": {
                    "number_of_genes": 2524,
                    "number_of_strs": 10,
                    "number_of_regions": 57
                },
                "types": [
                    {
                        "name": "Genetic Health Queensland",
                        "slug": "genetic-health-queensland",
                        "description": "Panel used by GHQ."
                    },
                    {
                        "name": "Victorian Clinical Genetics Services",
                        "slug": "victorian-clinical-genetics-services",
                        "description": "Panel used by VCGS."
                    },
                    {
                        "name": "Rare Disease",
                        "slug": "rare-disease",
                        "description": "Rare disease panels"
                    },
                    {
                        "name": "Royal Melbourne Hospital",
                        "slug": "royal-melbourne-hospital",
                        "description": "Royal Melbourne Hospital"
                    }
                ],
                "child_panel_ids": []
            },
            "transcript": null
        },
        {
            "gene_data": {
                "alias": [
                    "B22",
                    "UQOR22",
                    "LYRM3"
                ],
                "biotype": "protein_coding",
                "hgnc_id": "HGNC:7704",
                "gene_name": "NADH:ubiquinone oxidoreductase subunit B9",
                "omim_gene": [
                    "601445"
                ],
                "alias_name": [
                    "complex I B22 subunit"
                ],
                "gene_symbol": "NDUFB9",
                "hgnc_symbol": "NDUFB9",
                "hgnc_release": "2017-11-03",
                "ensembl_genes": {
                    "GRch37": {
                        "82": {
                            "location": "8:125551344-125580751",
                            "ensembl_id": "ENSG00000147684"
                        }
                    },
                    "GRch38": {
                        "90": {
                            "location": "8:124539103-124568510",
                            "ensembl_id": "ENSG00000147684"
                        }
                    }
                },
                "hgnc_date_symbol_changed": "1996-10-18"
            },
            "entity_type": "gene",
            "entity_name": "NDUFB9",
            "confidence_level": "2",
            "penetrance": null,
            "mode_of_pathogenicity": "",
            "publications": [
                "22200994",
                "38129218"
            ],
            "evidence": [
                "Expert Review Amber",
                "Genetic Health Queensland"
            ],
            "phenotypes": [
                "Mitochondrial complex I deficiency, nuclear type 24, MIM#618245"
            ],
            "mode_of_inheritance": "BIALLELIC, autosomal or pseudoautosomal",
            "tags": [],
            "panel": {
                "id": 250,
                "hash_id": null,
                "name": "Intellectual disability syndromic and non-syndromic",
                "disease_group": "Neurology and neurodevelopmental disorders",
                "disease_sub_group": "",
                "description": "This panel was created by merging the ID panels used by Genetic Health Queensland and by the Victorian Clinical Genetics Services. Discrepant gene classifications reviewed and resolved by Chirag Patel and Zornitza Stark.\r\n\r\nThis is a consensus panel used by VCGS, GHQ and RMH.\r\n\r\nThis panel has been compared against the Genomics England PanelApp Intellectual Disability panel, and all discrepancies have been resolved, with reciprocal reviews provided to Genomics England, 11/3/2020.",
                "status": "public",
                "version": "1.760",
                "version_created": "2026-04-26T17:50:23.271073+10:00",
                "relevant_disorders": [
                    "Intellectual disability",
                    "HP:0001249; Neurodevelopmental delay",
                    "HP:0012758"
                ],
                "stats": {
                    "number_of_genes": 2524,
                    "number_of_strs": 10,
                    "number_of_regions": 57
                },
                "types": [
                    {
                        "name": "Genetic Health Queensland",
                        "slug": "genetic-health-queensland",
                        "description": "Panel used by GHQ."
                    },
                    {
                        "name": "Victorian Clinical Genetics Services",
                        "slug": "victorian-clinical-genetics-services",
                        "description": "Panel used by VCGS."
                    },
                    {
                        "name": "Rare Disease",
                        "slug": "rare-disease",
                        "description": "Rare disease panels"
                    },
                    {
                        "name": "Royal Melbourne Hospital",
                        "slug": "royal-melbourne-hospital",
                        "description": "Royal Melbourne Hospital"
                    }
                ],
                "child_panel_ids": []
            },
            "transcript": null
        },
        {
            "gene_data": {
                "alias": [
                    "CI-75k"
                ],
                "biotype": "protein_coding",
                "hgnc_id": "HGNC:7707",
                "gene_name": "NADH:ubiquinone oxidoreductase core subunit S1",
                "omim_gene": [
                    "157655"
                ],
                "alias_name": [
                    "complex I 75kDa subunit",
                    "NADH-ubiquinone oxidoreductase 75 kDa subunit, mitochondrial"
                ],
                "gene_symbol": "NDUFS1",
                "hgnc_symbol": "NDUFS1",
                "hgnc_release": "2017-11-03",
                "ensembl_genes": {
                    "GRch37": {
                        "82": {
                            "location": "2:206979541-207024327",
                            "ensembl_id": "ENSG00000023228"
                        }
                    },
                    "GRch38": {
                        "90": {
                            "location": "2:206114817-206159603",
                            "ensembl_id": "ENSG00000023228"
                        }
                    }
                },
                "hgnc_date_symbol_changed": "1992-04-03"
            },
            "entity_type": "gene",
            "entity_name": "NDUFS1",
            "confidence_level": "3",
            "penetrance": null,
            "mode_of_pathogenicity": "",
            "publications": [
                "20382551"
            ],
            "evidence": [
                "Expert Review Green",
                "Genetic Health Queensland"
            ],
            "phenotypes": [
                "Mitochondrial complex I deficiency, nuclear type 5, MIM# 618226"
            ],
            "mode_of_inheritance": "BIALLELIC, autosomal or pseudoautosomal",
            "tags": [],
            "panel": {
                "id": 250,
                "hash_id": null,
                "name": "Intellectual disability syndromic and non-syndromic",
                "disease_group": "Neurology and neurodevelopmental disorders",
                "disease_sub_group": "",
                "description": "This panel was created by merging the ID panels used by Genetic Health Queensland and by the Victorian Clinical Genetics Services. Discrepant gene classifications reviewed and resolved by Chirag Patel and Zornitza Stark.\r\n\r\nThis is a consensus panel used by VCGS, GHQ and RMH.\r\n\r\nThis panel has been compared against the Genomics England PanelApp Intellectual Disability panel, and all discrepancies have been resolved, with reciprocal reviews provided to Genomics England, 11/3/2020.",
                "status": "public",
                "version": "1.760",
                "version_created": "2026-04-26T17:50:23.271073+10:00",
                "relevant_disorders": [
                    "Intellectual disability",
                    "HP:0001249; Neurodevelopmental delay",
                    "HP:0012758"
                ],
                "stats": {
                    "number_of_genes": 2524,
                    "number_of_strs": 10,
                    "number_of_regions": 57
                },
                "types": [
                    {
                        "name": "Genetic Health Queensland",
                        "slug": "genetic-health-queensland",
                        "description": "Panel used by GHQ."
                    },
                    {
                        "name": "Victorian Clinical Genetics Services",
                        "slug": "victorian-clinical-genetics-services",
                        "description": "Panel used by VCGS."
                    },
                    {
                        "name": "Rare Disease",
                        "slug": "rare-disease",
                        "description": "Rare disease panels"
                    },
                    {
                        "name": "Royal Melbourne Hospital",
                        "slug": "royal-melbourne-hospital",
                        "description": "Royal Melbourne Hospital"
                    }
                ],
                "child_panel_ids": []
            },
            "transcript": null
        },
        {
            "gene_data": {
                "alias": [
                    "CI-49"
                ],
                "biotype": "protein_coding",
                "hgnc_id": "HGNC:7708",
                "gene_name": "NADH:ubiquinone oxidoreductase core subunit S2",
                "omim_gene": [
                    "602985"
                ],
                "alias_name": [
                    "complex I 49kDa subunit",
                    "NADH dehydrogenase [ubiquinone] iron-sulfur protein 2, mitochondrial"
                ],
                "gene_symbol": "NDUFS2",
                "hgnc_symbol": "NDUFS2",
                "hgnc_release": "2017-11-03",
                "ensembl_genes": {
                    "GRch37": {
                        "82": {
                            "location": "1:161166894-161184185",
                            "ensembl_id": "ENSG00000158864"
                        }
                    },
                    "GRch38": {
                        "90": {
                            "location": "1:161197104-161214395",
                            "ensembl_id": "ENSG00000158864"
                        }
                    }
                },
                "hgnc_date_symbol_changed": "1992-06-30"
            },
            "entity_type": "gene",
            "entity_name": "NDUFS2",
            "confidence_level": "2",
            "penetrance": null,
            "mode_of_pathogenicity": "",
            "publications": [
                "11220739",
                "31411514",
                "29272804"
            ],
            "evidence": [
                "Expert Review Amber",
                "Genetic Health Queensland"
            ],
            "phenotypes": [
                "Mitochondrial complex I deficiency, nuclear type 6, MIM#618228"
            ],
            "mode_of_inheritance": "BIALLELIC, autosomal or pseudoautosomal",
            "tags": [],
            "panel": {
                "id": 250,
                "hash_id": null,
                "name": "Intellectual disability syndromic and non-syndromic",
                "disease_group": "Neurology and neurodevelopmental disorders",
                "disease_sub_group": "",
                "description": "This panel was created by merging the ID panels used by Genetic Health Queensland and by the Victorian Clinical Genetics Services. Discrepant gene classifications reviewed and resolved by Chirag Patel and Zornitza Stark.\r\n\r\nThis is a consensus panel used by VCGS, GHQ and RMH.\r\n\r\nThis panel has been compared against the Genomics England PanelApp Intellectual Disability panel, and all discrepancies have been resolved, with reciprocal reviews provided to Genomics England, 11/3/2020.",
                "status": "public",
                "version": "1.760",
                "version_created": "2026-04-26T17:50:23.271073+10:00",
                "relevant_disorders": [
                    "Intellectual disability",
                    "HP:0001249; Neurodevelopmental delay",
                    "HP:0012758"
                ],
                "stats": {
                    "number_of_genes": 2524,
                    "number_of_strs": 10,
                    "number_of_regions": 57
                },
                "types": [
                    {
                        "name": "Genetic Health Queensland",
                        "slug": "genetic-health-queensland",
                        "description": "Panel used by GHQ."
                    },
                    {
                        "name": "Victorian Clinical Genetics Services",
                        "slug": "victorian-clinical-genetics-services",
                        "description": "Panel used by VCGS."
                    },
                    {
                        "name": "Rare Disease",
                        "slug": "rare-disease",
                        "description": "Rare disease panels"
                    },
                    {
                        "name": "Royal Melbourne Hospital",
                        "slug": "royal-melbourne-hospital",
                        "description": "Royal Melbourne Hospital"
                    }
                ],
                "child_panel_ids": []
            },
            "transcript": null
        }
    ]
}