Search Genes

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                "alias": [
                    "PHKD"
                ],
                "biotype": "protein_coding",
                "hgnc_id": "HGNC:1449",
                "gene_name": "calmodulin 3",
                "omim_gene": [
                    "114183"
                ],
                "alias_name": [
                    "prepro-calmodulin 3",
                    "phosphorylase kinase subunit delta"
                ],
                "gene_symbol": "CALM3",
                "hgnc_symbol": "CALM3",
                "hgnc_release": "2017-11-03",
                "ensembl_genes": {
                    "GRch37": {
                        "82": {
                            "location": "19:47104331-47114050",
                            "ensembl_id": "ENSG00000160014"
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                "hgnc_date_symbol_changed": "1991-06-05"
            },
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                "25460178",
                "31454269"
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                "Expert Review Green",
                "Expert list"
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            "phenotypes": [
                "Long QT syndrome 16, MIM# 618782"
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                "id": 4126,
                "hash_id": null,
                "name": "Transplant Co-Morbidity",
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                        "name": "Royal Melbourne Hospital",
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        },
        {
            "gene_data": {
                "alias": [
                    "PHKD",
                    "CAMII"
                ],
                "biotype": "protein_coding",
                "hgnc_id": "HGNC:1445",
                "gene_name": "calmodulin 2",
                "omim_gene": [
                    "114182"
                ],
                "alias_name": [
                    "prepro-calmodulin 2",
                    "phosphorylase kinase subunit delta"
                ],
                "gene_symbol": "CALM2",
                "hgnc_symbol": "CALM2",
                "hgnc_release": "2017-11-03",
                "ensembl_genes": {
                    "GRch37": {
                        "82": {
                            "location": "2:47387221-47403740",
                            "ensembl_id": "ENSG00000143933"
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            "entity_name": "CALM2",
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                "31983240",
                "31170290"
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                "Expert Review Green",
                "Victorian Clinical Genetics Services"
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            "phenotypes": [
                "Long QT syndrome 15 616249",
                "idopathic VF",
                "sudden unexplained death"
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        {
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                "alias": [
                    "CAMI",
                    "PHKD",
                    "DD132"
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                "biotype": "protein_coding",
                "hgnc_id": "HGNC:1442",
                "gene_name": "calmodulin 1",
                "omim_gene": [
                    "114180"
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                "alias_name": [
                    "prepro-calmodulin 1",
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                ],
                "gene_symbol": "CALM1",
                "hgnc_symbol": "CALM1",
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                "ensembl_genes": {
                    "GRch37": {
                        "82": {
                            "location": "14:90862846-90874605",
                            "ensembl_id": "ENSG00000198668"
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                "31170290"
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                "Expert Review Green",
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            "phenotypes": [
                "Long QT syndrome 14 616247",
                "Ventricular tachycardia, catecholaminergic polymorphic, 4 614916"
            ],
            "mode_of_inheritance": "MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted",
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                "status": "public",
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                        "slug": "melbourne-genomics",
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                        "name": "Royal Melbourne Hospital",
                        "slug": "royal-melbourne-hospital",
                        "description": "Royal Melbourne Hospital"
                    }
                ],
                "child_panel_ids": []
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            "transcript": null
        },
        {
            "gene_data": {
                "alias": [
                    "Cav1.1",
                    "hypoPP"
                ],
                "biotype": "protein_coding",
                "hgnc_id": "HGNC:1397",
                "gene_name": "calcium voltage-gated channel subunit alpha1 S",
                "omim_gene": [
                    "114208"
                ],
                "alias_name": null,
                "gene_symbol": "CACNA1S",
                "hgnc_symbol": "CACNA1S",
                "hgnc_release": "2017-11-03",
                "ensembl_genes": {
                    "GRch37": {
                        "82": {
                            "location": "1:201008642-201081694",
                            "ensembl_id": "ENSG00000081248"
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                    },
                    "GRch38": {
                        "90": {
                            "location": "1:201039512-201112566",
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                },
                "hgnc_date_symbol_changed": "1992-03-27"
            },
            "entity_type": "gene",
            "entity_name": "CACNA1S",
            "confidence_level": "3",
            "penetrance": null,
            "mode_of_pathogenicity": "",
            "publications": [],
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                "Expert Review Green",
                "Melbourne Genomics Health Alliance"
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            "phenotypes": [
                "Malignant hyperthermia susceptibility 5, MIM# 601887"
            ],
            "mode_of_inheritance": "MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted",
            "tags": [],
            "panel": {
                "id": 4126,
                "hash_id": null,
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                "disease_sub_group": "",
                "description": "This panel was built for the Melbourne Genomics Health Alliance Transplant Clinical Change Project. It contains genes from the following panels, that may be actionable in the study cohort:\r\n- cardiomyopathy and arrhythmia adult superpanels\r\n- additional findings adult panel, minus STK11, MUTYH, BTD, OTC, GAA, RPE65\r\n- AD nonsyndromic monogenic diabetes genes\r\n- dyslipidaemia\r\n- osteogenesis imperfecta\r\n- bleeding & platelet disorders\r\n- melanoma",
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                    }
                ],
                "child_panel_ids": []
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            "transcript": null
        },
        {
            "gene_data": {
                "alias": [
                    "Cav1.2",
                    "CACH2",
                    "CACN2",
                    "TS",
                    "LQT8"
                ],
                "biotype": "protein_coding",
                "hgnc_id": "HGNC:1390",
                "gene_name": "calcium voltage-gated channel subunit alpha1 C",
                "omim_gene": [
                    "114205"
                ],
                "alias_name": null,
                "gene_symbol": "CACNA1C",
                "hgnc_symbol": "CACNA1C",
                "hgnc_release": "2017-11-03",
                "ensembl_genes": {
                    "GRch37": {
                        "82": {
                            "location": "12:2079952-2802108",
                            "ensembl_id": "ENSG00000151067"
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                    },
                    "GRch38": {
                        "90": {
                            "location": "12:1970786-2697950",
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                },
                "hgnc_date_symbol_changed": "1991-01-30"
            },
            "entity_type": "gene",
            "entity_name": "CACNA1C",
            "confidence_level": "3",
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            "mode_of_pathogenicity": "",
            "publications": [
                "31983240"
            ],
            "evidence": [
                "Expert Review Green",
                "Victorian Clinical Genetics Services"
            ],
            "phenotypes": [
                "Long QT syndrome 8, MIM# 618447",
                "Timothy syndrome, MIM# 601005"
            ],
            "mode_of_inheritance": "MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted",
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                "id": 4126,
                "hash_id": null,
                "name": "Transplant Co-Morbidity",
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                "description": "This panel was built for the Melbourne Genomics Health Alliance Transplant Clinical Change Project. It contains genes from the following panels, that may be actionable in the study cohort:\r\n- cardiomyopathy and arrhythmia adult superpanels\r\n- additional findings adult panel, minus STK11, MUTYH, BTD, OTC, GAA, RPE65\r\n- AD nonsyndromic monogenic diabetes genes\r\n- dyslipidaemia\r\n- osteogenesis imperfecta\r\n- bleeding & platelet disorders\r\n- melanoma",
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                        "name": "Royal Melbourne Hospital",
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                    }
                ],
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            "transcript": null
        },
        {
            "gene_data": {
                "alias": [
                    "gC1Q-R",
                    "gC1qR",
                    "p32",
                    "SF2p32"
                ],
                "biotype": "protein_coding",
                "hgnc_id": "HGNC:1243",
                "gene_name": "complement C1q binding protein",
                "omim_gene": [
                    "601269"
                ],
                "alias_name": [
                    "C1q globular domain-binding protein",
                    "hyaluronan-binding protein 1",
                    "splicing factor SF2-associated protein"
                ],
                "gene_symbol": "C1QBP",
                "hgnc_symbol": "C1QBP",
                "hgnc_release": "2017-11-03",
                "ensembl_genes": {
                    "GRch37": {
                        "82": {
                            "location": "17:5336097-5352150",
                            "ensembl_id": "ENSG00000108561"
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                    },
                    "GRch38": {
                        "90": {
                            "location": "17:5432777-5448830",
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                },
                "hgnc_date_symbol_changed": "1995-12-11"
            },
            "entity_type": "gene",
            "entity_name": "C1QBP",
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            "mode_of_pathogenicity": "",
            "publications": [
                "28942965"
            ],
            "evidence": [
                "Expert Review Green",
                "Expert list"
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            "phenotypes": [
                "Combined oxidative phosphorylation deficiency 33, MIM#617713"
            ],
            "mode_of_inheritance": "BIALLELIC, autosomal or pseudoautosomal",
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                "id": 4126,
                "hash_id": null,
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                    }
                ],
                "child_panel_ids": []
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        },
        {
            "gene_data": {
                "alias": [
                    "FAD",
                    "FAD1",
                    "BRCC2",
                    "XRCC11"
                ],
                "biotype": "protein_coding",
                "hgnc_id": "HGNC:1101",
                "gene_name": "BRCA2, DNA repair associated",
                "omim_gene": [
                    "600185"
                ],
                "alias_name": [
                    "BRCA1/BRCA2-containing complex, subunit 2"
                ],
                "gene_symbol": "BRCA2",
                "hgnc_symbol": "BRCA2",
                "hgnc_release": "2017-11-03",
                "ensembl_genes": {
                    "GRch37": {
                        "82": {
                            "location": "13:32889611-32973805",
                            "ensembl_id": "ENSG00000139618"
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                    },
                    "GRch38": {
                        "90": {
                            "location": "13:32315474-32400266",
                            "ensembl_id": "ENSG00000139618"
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                },
                "hgnc_date_symbol_changed": "1994-10-17"
            },
            "entity_type": "gene",
            "entity_name": "BRCA2",
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                "Expert Review Green",
                "Melbourne Genomics Health Alliance"
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            "phenotypes": [
                "Breast-ovarian cancer, familial, 2, MIM#612555"
            ],
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        {
            "gene_data": {
                "alias": [
                    "RNF53",
                    "BRCC1",
                    "PPP1R53",
                    "FANCS"
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                "hgnc_id": "HGNC:1100",
                "gene_name": "BRCA1, DNA repair associated",
                "omim_gene": [
                    "113705"
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                "alias_name": [
                    "BRCA1/BRCA2-containing complex, subunit 1",
                    "protein phosphatase 1, regulatory subunit 53",
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                "gene_symbol": "BRCA1",
                "hgnc_symbol": "BRCA1",
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                "ensembl_genes": {
                    "GRch37": {
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                            "location": "17:41196312-41277500",
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                    "ALK3",
                    "CD292"
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                },
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                        "name": "Royal Melbourne Hospital",
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                        "name": "Melbourne Genomics",
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                        "name": "Royal Melbourne Hospital",
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                "child_panel_ids": []
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        },
        {
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                "biotype": "protein_coding",
                "hgnc_id": "HGNC:17978",
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                    "615291"
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                    "beta-1,3-galactosyltransferase-6"
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                            "location": "1:1167629-1170421",
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                "23664118",
                "23664117"
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                        "name": "Royal Melbourne Hospital",
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                ],
                "child_panel_ids": []
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        },
        {
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                "alias": [],
                "biotype": "protein_coding",
                "hgnc_id": "HGNC:870",
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                    "606882"
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                    "copper-transporting ATPase 2"
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                    "GRch37": {
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                            "location": "13:52506809-52585630",
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                            "location": "13:51930436-52012125",
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                "hgnc_date_symbol_changed": "1986-01-01"
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            "entity_type": "gene",
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                "Melbourne Genomics Health Alliance"
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            "panel": {
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                "types": [
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                        "name": "Melbourne Genomics",
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                        "name": "Royal Melbourne Hospital",
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                "child_panel_ids": []
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        },
        {
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                    "ARC41",
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                    "p41-ARC"
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                "biotype": "protein_coding",
                "hgnc_id": "HGNC:704",
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                "omim_gene": [
                    "604223"
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                "alias_name": [
                    "ARP2/3 protein complex subunit p41",
                    "actin related protein 2/3 complex, subunit 1A (41 kD)"
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                    "GRch37": {
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                            "location": "7:98971872-98992424",
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                "hgnc_date_symbol_changed": "1999-08-06"
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                "30254128"
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                "Expert Review Green"
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            "mode_of_inheritance": "BIALLELIC, autosomal or pseudoautosomal",
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            "panel": {
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                "types": [
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                        "name": "Melbourne Genomics",
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                        "name": "Royal Melbourne Hospital",
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                "child_panel_ids": []
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            "transcript": null
        },
        {
            "gene_data": {
                "alias": [],
                "biotype": "protein_coding",
                "hgnc_id": "HGNC:613",
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                    "107741"
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                "alias_name": null,
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                "hgnc_symbol": "APOE",
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                "ensembl_genes": {
                    "GRch37": {
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                            "location": "19:45409011-45412650",
                            "ensembl_id": "ENSG00000130203"
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                    },
                    "GRch38": {
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                "hgnc_date_symbol_changed": "2001-06-22"
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            "entity_type": "gene",
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                "Expert Review Green",
                "Royal Melbourne Hospital"
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                "Sea-blue histiocyte disease, Dysbetalipoproteinemia, familial (Hyperlipoproteinemia), Lipoprotein glomerulopathy"
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            "mode_of_inheritance": "BOTH monoallelic and biallelic, autosomal or pseudoautosomal",
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            "panel": {
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                "types": [
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                "child_panel_ids": []
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        {
            "gene_data": {
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                "biotype": "protein_coding",
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                "alias_name": null,
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                "hgnc_symbol": "APOC2",
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                "ensembl_genes": {
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                "hgnc_date_symbol_changed": "2001-06-22"
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            "entity_type": "gene",
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                "child_panel_ids": []
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        },
        {
            "gene_data": {
                "alias": [],
                "biotype": "protein_coding",
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                "ensembl_genes": {
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                    },
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                "child_panel_ids": []
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        {
            "gene_data": {
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                    "RAP3",
                    "APOA-V"
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                            "location": "11:116660083-116663136",
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                "child_panel_ids": []
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        {
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        {
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                        "description": "Royal Melbourne Hospital"
                    }
                ],
                "child_panel_ids": []
            },
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        },
        {
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                    "P450IIC19",
                    "CPCJ"
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                "hgnc_id": "HGNC:2621",
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                    "124020"
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                "hgnc_date_symbol_changed": "1992-04-06"
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            "entity_type": "gene",
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                "12464799"
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                "Expert Review Green",
                "Expert list"
            ],
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                "DRUG METABOLISM, POOR, CYP2C19-RELATED, MEPHENYTOIN, POOR METABOLISM OF, INCLUDED OMEPRAZOLE, POOR METABOLISM OF, INCLUDED PROGUANIL, POOR METABOLISM OF, INCLUDED CLOPIDOGREL, POOR METABOLISM OF, INCLUDED MIM#609535"
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                },
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                    {
                        "name": "Royal Melbourne Hospital",
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                ],
                "child_panel_ids": []
            },
            "transcript": null
        },
        {
            "gene_data": {
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                    "MRP7",
                    "ABC35",
                    "TNR-CFTR",
                    "dJ760C5.1",
                    "CFTR/MRP"
                ],
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                "hgnc_id": "HGNC:1884",
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                "omim_gene": [
                    "602421"
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                ],
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                "hgnc_symbol": "CFTR",
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                "ensembl_genes": {
                    "GRch37": {
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                            "location": "7:117105838-117356025",
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                },
                "hgnc_date_symbol_changed": "1986-01-01"
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            "entity_type": "gene",
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                "Congenital bilateral absence of vas deferens MIM#277180",
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            "panel": {
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                },
                "types": [
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                    {
                        "name": "Royal Melbourne Hospital",
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                ],
                "child_panel_ids": []
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            "transcript": null
        },
        {
            "gene_data": {
                "alias": [
                    "PCN3",
                    "P450PCN3",
                    "CP35"
                ],
                "biotype": "protein_coding",
                "hgnc_id": "HGNC:2638",
                "gene_name": "cytochrome P450 family 3 subfamily A member 5",
                "omim_gene": [
                    "605325"
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                "alias_name": null,
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                "hgnc_symbol": "CYP3A5",
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                "ensembl_genes": {
                    "GRch37": {
                        "82": {
                            "location": "7:99245817-99277621",
                            "ensembl_id": "ENSG00000106258"
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                },
                "hgnc_date_symbol_changed": "1990-02-24"
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            "entity_type": "gene",
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                "Expert Review Green",
                "Expert list"
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                "Hypertension, salt-sensitive essential, susceptibility to MIM#145500"
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            "panel": {
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                "version": "0.21",
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                "types": [
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                        "name": "Melbourne Genomics",
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                        "name": "Royal Melbourne Hospital",
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                "child_panel_ids": []
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        {
            "gene_data": {
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                "hgnc_id": "HGNC:12014",
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                "hgnc_symbol": "TPMT",
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                "ensembl_genes": {
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                "hgnc_date_symbol_changed": "1993-08-25"
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            "entity_type": "gene",
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                "Expert Review Green",
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                "Thiopurines, poor metabolism of, 1 MIM# 610460"
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                "child_panel_ids": []
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            "transcript": null
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        {
            "gene_data": {
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                "biotype": "protein_coding",
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                "omim_gene": [
                    "191740"
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                "ensembl_genes": {
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                            "location": "2:234526291-234681956",
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                    },
                    "GRch38": {
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                "hgnc_date_symbol_changed": "1989-02-13"
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            "entity_type": "gene",
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                "Expert Review Green",
                "Expert list"
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                "Crigler-Najjar syndrome, type II MIM#606785"
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            "panel": {
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                ],
                "child_panel_ids": []
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            "transcript": null
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        {
            "gene_data": {
                "alias": [
                    "DPD"
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                "biotype": "protein_coding",
                "hgnc_id": "HGNC:3012",
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                    "612779"
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                "alias_name": null,
                "gene_symbol": "DPYD",
                "hgnc_symbol": "DPYD",
                "hgnc_release": "2017-11-03",
                "ensembl_genes": {
                    "GRch37": {
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                            "location": "1:97543299-98386605",
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                    },
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            "entity_type": "gene",
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                "Expert Review Green",
                "Expert list"
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            "panel": {
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                ],
                "child_panel_ids": []
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        },
        {
            "gene_data": {
                "alias": [
                    "XT-II",
                    "PXYLT2"
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                "biotype": "protein_coding",
                "hgnc_id": "HGNC:15517",
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                "omim_gene": [
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                "alias_name": [
                    "protein xylosyltransferase 2"
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                "gene_symbol": "XYLT2",
                "hgnc_symbol": "XYLT2",
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                "ensembl_genes": {
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                            "location": "17:48423453-48440499",
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                },
                "hgnc_date_symbol_changed": "2001-04-06"
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            "entity_type": "gene",
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            "panel": {
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                "child_panel_ids": []
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        {
            "gene_data": {
                "alias": [
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                "biotype": "protein_coding",
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                "gene_name": "Wilms tumor 1",
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                "alias_name": null,
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                "hgnc_symbol": "WT1",
                "hgnc_release": "2017-11-03",
                "ensembl_genes": {
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                            "location": "11:32409321-32457176",
                            "ensembl_id": "ENSG00000184937"
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                    },
                    "GRch38": {
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                "hgnc_date_symbol_changed": "1989-04-13"
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            "entity_type": "gene",
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            "panel": {
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                "child_panel_ids": []
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        {
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            "mode_of_inheritance": "BIALLELIC, autosomal or pseudoautosomal",
            "tags": [],
            "panel": {
                "id": 4126,
                "hash_id": null,
                "name": "Transplant Co-Morbidity",
                "disease_group": "Screening",
                "disease_sub_group": "",
                "description": "This panel was built for the Melbourne Genomics Health Alliance Transplant Clinical Change Project. It contains genes from the following panels, that may be actionable in the study cohort:\r\n- cardiomyopathy and arrhythmia adult superpanels\r\n- additional findings adult panel, minus STK11, MUTYH, BTD, OTC, GAA, RPE65\r\n- AD nonsyndromic monogenic diabetes genes\r\n- dyslipidaemia\r\n- osteogenesis imperfecta\r\n- bleeding & platelet disorders\r\n- melanoma",
                "status": "public",
                "version": "0.21",
                "version_created": "2026-01-16T12:00:12.269232+11:00",
                "relevant_disorders": [],
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                    "number_of_genes": 278,
                    "number_of_strs": 0,
                    "number_of_regions": 0
                },
                "types": [
                    {
                        "name": "Melbourne Genomics",
                        "slug": "melbourne-genomics",
                        "description": "Panel used by a Melbourne Genomics project."
                    },
                    {
                        "name": "Royal Melbourne Hospital",
                        "slug": "royal-melbourne-hospital",
                        "description": "Royal Melbourne Hospital"
                    }
                ],
                "child_panel_ids": []
            },
            "transcript": null
        },
        {
            "gene_data": {
                "alias": [
                    "WIP"
                ],
                "biotype": "protein_coding",
                "hgnc_id": "HGNC:12736",
                "gene_name": "WAS/WASL interacting protein family member 1",
                "omim_gene": [
                    "602357"
                ],
                "alias_name": null,
                "gene_symbol": "WIPF1",
                "hgnc_symbol": "WIPF1",
                "hgnc_release": "2017-11-03",
                "ensembl_genes": {
                    "GRch37": {
                        "82": {
                            "location": "2:175424300-175547644",
                            "ensembl_id": "ENSG00000115935"
                        }
                    },
                    "GRch38": {
                        "90": {
                            "location": "2:174559572-174682916",
                            "ensembl_id": "ENSG00000115935"
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                    }
                },
                "hgnc_date_symbol_changed": "2006-10-12"
            },
            "entity_type": "gene",
            "entity_name": "WIPF1",
            "confidence_level": "3",
            "penetrance": null,
            "mode_of_pathogenicity": "",
            "publications": [
                "11869681",
                "14757742",
                "9405671",
                "27742395",
                "22231303"
            ],
            "evidence": [
                "Expert list",
                "Expert Review Green"
            ],
            "phenotypes": [
                "Wiskott-Aldrich syndrome 2, MIM# 614493"
            ],
            "mode_of_inheritance": "BIALLELIC, autosomal or pseudoautosomal",
            "tags": [],
            "panel": {
                "id": 4126,
                "hash_id": null,
                "name": "Transplant Co-Morbidity",
                "disease_group": "Screening",
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                "description": "This panel was built for the Melbourne Genomics Health Alliance Transplant Clinical Change Project. It contains genes from the following panels, that may be actionable in the study cohort:\r\n- cardiomyopathy and arrhythmia adult superpanels\r\n- additional findings adult panel, minus STK11, MUTYH, BTD, OTC, GAA, RPE65\r\n- AD nonsyndromic monogenic diabetes genes\r\n- dyslipidaemia\r\n- osteogenesis imperfecta\r\n- bleeding & platelet disorders\r\n- melanoma",
                "status": "public",
                "version": "0.21",
                "version_created": "2026-01-16T12:00:12.269232+11:00",
                "relevant_disorders": [],
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                    "number_of_genes": 278,
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                    "number_of_regions": 0
                },
                "types": [
                    {
                        "name": "Melbourne Genomics",
                        "slug": "melbourne-genomics",
                        "description": "Panel used by a Melbourne Genomics project."
                    },
                    {
                        "name": "Royal Melbourne Hospital",
                        "slug": "royal-melbourne-hospital",
                        "description": "Royal Melbourne Hospital"
                    }
                ],
                "child_panel_ids": []
            },
            "transcript": null
        },
        {
            "gene_data": {
                "alias": [
                    "DIDMOAD",
                    "WFS"
                ],
                "biotype": "protein_coding",
                "hgnc_id": "HGNC:12762",
                "gene_name": "wolframin ER transmembrane glycoprotein",
                "omim_gene": [
                    "606201"
                ],
                "alias_name": null,
                "gene_symbol": "WFS1",
                "hgnc_symbol": "WFS1",
                "hgnc_release": "2017-11-03",
                "ensembl_genes": {
                    "GRch37": {
                        "82": {
                            "location": "4:6271576-6304992",
                            "ensembl_id": "ENSG00000109501"
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                    },
                    "GRch38": {
                        "90": {
                            "location": "4:6269849-6303265",
                            "ensembl_id": "ENSG00000109501"
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                    }
                },
                "hgnc_date_symbol_changed": "1995-01-30"
            },
            "entity_type": "gene",
            "entity_name": "WFS1",
            "confidence_level": "3",
            "penetrance": null,
            "mode_of_pathogenicity": "",
            "publications": [
                "27217304",
                "27185633"
            ],
            "evidence": [
                "Expert Review Green",
                "NHS GMS"
            ],
            "phenotypes": [
                "diabetes insipidus or optic atrophy",
                "?Cataract 41,116400",
                "Wolfram syndrome, 222300",
                "Deafness,autosomal dominant 6/14/38, 600965",
                "{Diabetes mellitus, noninsulin-dependent, association with}, 125853",
                "{Diabetes mellitus, noninsulin-dependent,association with}",
                "Deafness, autosomal dominant 6/14/38, 600965",
                "Wolfram-like syndrome, autosomal dominant, 614296"
            ],
            "mode_of_inheritance": "BOTH monoallelic and biallelic, autosomal or pseudoautosomal",
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            "panel": {
                "id": 4126,
                "hash_id": null,
                "name": "Transplant Co-Morbidity",
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                "disease_sub_group": "",
                "description": "This panel was built for the Melbourne Genomics Health Alliance Transplant Clinical Change Project. It contains genes from the following panels, that may be actionable in the study cohort:\r\n- cardiomyopathy and arrhythmia adult superpanels\r\n- additional findings adult panel, minus STK11, MUTYH, BTD, OTC, GAA, RPE65\r\n- AD nonsyndromic monogenic diabetes genes\r\n- dyslipidaemia\r\n- osteogenesis imperfecta\r\n- bleeding & platelet disorders\r\n- melanoma",
                "status": "public",
                "version": "0.21",
                "version_created": "2026-01-16T12:00:12.269232+11:00",
                "relevant_disorders": [],
                "stats": {
                    "number_of_genes": 278,
                    "number_of_strs": 0,
                    "number_of_regions": 0
                },
                "types": [
                    {
                        "name": "Melbourne Genomics",
                        "slug": "melbourne-genomics",
                        "description": "Panel used by a Melbourne Genomics project."
                    },
                    {
                        "name": "Royal Melbourne Hospital",
                        "slug": "royal-melbourne-hospital",
                        "description": "Royal Melbourne Hospital"
                    }
                ],
                "child_panel_ids": []
            },
            "transcript": null
        },
        {
            "gene_data": {
                "alias": [
                    "WASP",
                    "WASPA"
                ],
                "biotype": "protein_coding",
                "hgnc_id": "HGNC:12731",
                "gene_name": "Wiskott-Aldrich syndrome",
                "omim_gene": [
                    "300392"
                ],
                "alias_name": [
                    "eczema-thrombocytopenia"
                ],
                "gene_symbol": "WAS",
                "hgnc_symbol": "WAS",
                "hgnc_release": "2017-11-03",
                "ensembl_genes": {
                    "GRch37": {
                        "82": {
                            "location": "X:48534985-48549818",
                            "ensembl_id": "ENSG00000015285"
                        }
                    },
                    "GRch38": {
                        "90": {
                            "location": "X:48676596-48691427",
                            "ensembl_id": "ENSG00000015285"
                        }
                    }
                },
                "hgnc_date_symbol_changed": "2001-06-22"
            },
            "entity_type": "gene",
            "entity_name": "WAS",
            "confidence_level": "3",
            "penetrance": null,
            "mode_of_pathogenicity": "",
            "publications": [],
            "evidence": [
                "Expert list",
                "Expert Review Green"
            ],
            "phenotypes": [
                "Wiskott-Aldrich syndrome, MIM# 301000",
                "Thrombocytopenia, X-linked, MIM# 313900"
            ],
            "mode_of_inheritance": "X-LINKED: hemizygous mutation in males, biallelic mutations in females",
            "tags": [],
            "panel": {
                "id": 4126,
                "hash_id": null,
                "name": "Transplant Co-Morbidity",
                "disease_group": "Screening",
                "disease_sub_group": "",
                "description": "This panel was built for the Melbourne Genomics Health Alliance Transplant Clinical Change Project. It contains genes from the following panels, that may be actionable in the study cohort:\r\n- cardiomyopathy and arrhythmia adult superpanels\r\n- additional findings adult panel, minus STK11, MUTYH, BTD, OTC, GAA, RPE65\r\n- AD nonsyndromic monogenic diabetes genes\r\n- dyslipidaemia\r\n- osteogenesis imperfecta\r\n- bleeding & platelet disorders\r\n- melanoma",
                "status": "public",
                "version": "0.21",
                "version_created": "2026-01-16T12:00:12.269232+11:00",
                "relevant_disorders": [],
                "stats": {
                    "number_of_genes": 278,
                    "number_of_strs": 0,
                    "number_of_regions": 0
                },
                "types": [
                    {
                        "name": "Melbourne Genomics",
                        "slug": "melbourne-genomics",
                        "description": "Panel used by a Melbourne Genomics project."
                    },
                    {
                        "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:12726",
                "gene_name": "von Willebrand factor",
                "omim_gene": [
                    "613160"
                ],
                "alias_name": null,
                "gene_symbol": "VWF",
                "hgnc_symbol": "VWF",
                "hgnc_release": "2017-11-03",
                "ensembl_genes": {
                    "GRch37": {
                        "82": {
                            "location": "12:6058040-6233936",
                            "ensembl_id": "ENSG00000110799"
                        }
                    },
                    "GRch38": {
                        "90": {
                            "location": "12:5948874-6124770",
                            "ensembl_id": "ENSG00000110799"
                        }
                    }
                },
                "hgnc_date_symbol_changed": "1986-01-01"
            },
            "entity_type": "gene",
            "entity_name": "VWF",
            "confidence_level": "3",
            "penetrance": null,
            "mode_of_pathogenicity": "",
            "publications": [],
            "evidence": [
                "Expert Review Green",
                "Victorian Clinical Genetics Services"
            ],
            "phenotypes": [
                "von Willebrand disease, type 1, MIM#193400",
                "von Willibrand disease, type 3, MIM#277480",
                "von Willebrand disease, types 2A, 2B, 2M, and 2N, MIM#613554"
            ],
            "mode_of_inheritance": "BOTH monoallelic and biallelic, autosomal or pseudoautosomal",
            "tags": [],
            "panel": {
                "id": 4126,
                "hash_id": null,
                "name": "Transplant Co-Morbidity",
                "disease_group": "Screening",
                "disease_sub_group": "",
                "description": "This panel was built for the Melbourne Genomics Health Alliance Transplant Clinical Change Project. It contains genes from the following panels, that may be actionable in the study cohort:\r\n- cardiomyopathy and arrhythmia adult superpanels\r\n- additional findings adult panel, minus STK11, MUTYH, BTD, OTC, GAA, RPE65\r\n- AD nonsyndromic monogenic diabetes genes\r\n- dyslipidaemia\r\n- osteogenesis imperfecta\r\n- bleeding & platelet disorders\r\n- melanoma",
                "status": "public",
                "version": "0.21",
                "version_created": "2026-01-16T12:00:12.269232+11:00",
                "relevant_disorders": [],
                "stats": {
                    "number_of_genes": 278,
                    "number_of_strs": 0,
                    "number_of_regions": 0
                },
                "types": [
                    {
                        "name": "Melbourne Genomics",
                        "slug": "melbourne-genomics",
                        "description": "Panel used by a Melbourne Genomics project."
                    },
                    {
                        "name": "Royal Melbourne Hospital",
                        "slug": "royal-melbourne-hospital",
                        "description": "Royal Melbourne Hospital"
                    }
                ],
                "child_panel_ids": []
            },
            "transcript": null
        },
        {
            "gene_data": {
                "alias": [
                    "FLJ14848"
                ],
                "biotype": "protein_coding",
                "hgnc_id": "HGNC:12712",
                "gene_name": "VPS33B, late endosome and lysosome associated",
                "omim_gene": [
                    "608552"
                ],
                "alias_name": null,
                "gene_symbol": "VPS33B",
                "hgnc_symbol": "VPS33B",
                "hgnc_release": "2017-11-03",
                "ensembl_genes": {
                    "GRch37": {
                        "82": {
                            "location": "15:91541646-91565833",
                            "ensembl_id": "ENSG00000184056"
                        }
                    },
                    "GRch38": {
                        "90": {
                            "location": "15:90998416-91022603",
                            "ensembl_id": "ENSG00000184056"
                        }
                    }
                },
                "hgnc_date_symbol_changed": "1999-11-19"
            },
            "entity_type": "gene",
            "entity_name": "VPS33B",
            "confidence_level": "3",
            "penetrance": null,
            "mode_of_pathogenicity": "",
            "publications": [
                "26399659",
                "16896922"
            ],
            "evidence": [
                "Expert list",
                "Expert Review Green"
            ],
            "phenotypes": [
                "Arthrogryposis, renal dysfunction, and cholestasis 1, MIM# 208085"
            ],
            "mode_of_inheritance": "BIALLELIC, autosomal or pseudoautosomal",
            "tags": [],
            "panel": {
                "id": 4126,
                "hash_id": null,
                "name": "Transplant Co-Morbidity",
                "disease_group": "Screening",
                "disease_sub_group": "",
                "description": "This panel was built for the Melbourne Genomics Health Alliance Transplant Clinical Change Project. It contains genes from the following panels, that may be actionable in the study cohort:\r\n- cardiomyopathy and arrhythmia adult superpanels\r\n- additional findings adult panel, minus STK11, MUTYH, BTD, OTC, GAA, RPE65\r\n- AD nonsyndromic monogenic diabetes genes\r\n- dyslipidaemia\r\n- osteogenesis imperfecta\r\n- bleeding & platelet disorders\r\n- melanoma",
                "status": "public",
                "version": "0.21",
                "version_created": "2026-01-16T12:00:12.269232+11:00",
                "relevant_disorders": [],
                "stats": {
                    "number_of_genes": 278,
                    "number_of_strs": 0,
                    "number_of_regions": 0
                },
                "types": [
                    {
                        "name": "Melbourne Genomics",
                        "slug": "melbourne-genomics",
                        "description": "Panel used by a Melbourne Genomics project."
                    },
                    {
                        "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:23663",
                "gene_name": "vitamin K epoxide reductase complex subunit 1",
                "omim_gene": [
                    "608547"
                ],
                "alias_name": null,
                "gene_symbol": "VKORC1",
                "hgnc_symbol": "VKORC1",
                "hgnc_release": "2017-11-03",
                "ensembl_genes": {
                    "GRch37": {
                        "82": {
                            "location": "16:31102163-31107301",
                            "ensembl_id": "ENSG00000167397"
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                    },
                    "GRch38": {
                        "90": {
                            "location": "16:31090842-31095980",
                            "ensembl_id": "ENSG00000167397"
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                    }
                },
                "hgnc_date_symbol_changed": "2004-02-04"
            },
            "entity_type": "gene",
            "entity_name": "VKORC1",
            "confidence_level": "3",
            "penetrance": null,
            "mode_of_pathogenicity": "",
            "publications": [
                "14765194"
            ],
            "evidence": [
                "Expert list",
                "Expert Review Green"
            ],
            "phenotypes": [
                "Vitamin K-dependent clotting factors, combined deficiency of, 2, MIM# 607473"
            ],
            "mode_of_inheritance": "BIALLELIC, autosomal or pseudoautosomal",
            "tags": [],
            "panel": {
                "id": 4126,
                "hash_id": null,
                "name": "Transplant Co-Morbidity",
                "disease_group": "Screening",
                "disease_sub_group": "",
                "description": "This panel was built for the Melbourne Genomics Health Alliance Transplant Clinical Change Project. It contains genes from the following panels, that may be actionable in the study cohort:\r\n- cardiomyopathy and arrhythmia adult superpanels\r\n- additional findings adult panel, minus STK11, MUTYH, BTD, OTC, GAA, RPE65\r\n- AD nonsyndromic monogenic diabetes genes\r\n- dyslipidaemia\r\n- osteogenesis imperfecta\r\n- bleeding & platelet disorders\r\n- melanoma",
                "status": "public",
                "version": "0.21",
                "version_created": "2026-01-16T12:00:12.269232+11:00",
                "relevant_disorders": [],
                "stats": {
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                    "number_of_strs": 0,
                    "number_of_regions": 0
                },
                "types": [
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                        "name": "Melbourne Genomics",
                        "slug": "melbourne-genomics",
                        "description": "Panel used by a Melbourne Genomics project."
                    },
                    {
                        "name": "Royal Melbourne Hospital",
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                        "description": "Royal Melbourne Hospital"
                    }
                ],
                "child_panel_ids": []
            },
            "transcript": null
        },
        {
            "gene_data": {
                "alias": [
                    "VIPAR",
                    "VPS16B",
                    "SPE-39",
                    "SPE39",
                    "hSPE-39"
                ],
                "biotype": "protein_coding",
                "hgnc_id": "HGNC:20347",
                "gene_name": "VPS33B interacting protein, apical-basolateral polarity regulator, spe-39 homolog",
                "omim_gene": [
                    "613401"
                ],
                "alias_name": [
                    "VPS33B interacting protein, apical-basolateral polarity regulator"
                ],
                "gene_symbol": "VIPAS39",
                "hgnc_symbol": "VIPAS39",
                "hgnc_release": "2017-11-03",
                "ensembl_genes": {
                    "GRch37": {
                        "82": {
                            "location": "14:77893018-77924295",
                            "ensembl_id": "ENSG00000151445"
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                    },
                    "GRch38": {
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                            "location": "14:77426675-77457952",
                            "ensembl_id": "ENSG00000151445"
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                    }
                },
                "hgnc_date_symbol_changed": "2012-07-24"
            },
            "entity_type": "gene",
            "entity_name": "VIPAS39",
            "confidence_level": "3",
            "penetrance": null,
            "mode_of_pathogenicity": "",
            "publications": [],
            "evidence": [
                "Expert list",
                "Expert Review Green"
            ],
            "phenotypes": [
                "Arthrogryposis, renal dysfunction, and cholestasis 2, MIM# 613404"
            ],
            "mode_of_inheritance": "BIALLELIC, autosomal or pseudoautosomal",
            "tags": [],
            "panel": {
                "id": 4126,
                "hash_id": null,
                "name": "Transplant Co-Morbidity",
                "disease_group": "Screening",
                "disease_sub_group": "",
                "description": "This panel was built for the Melbourne Genomics Health Alliance Transplant Clinical Change Project. It contains genes from the following panels, that may be actionable in the study cohort:\r\n- cardiomyopathy and arrhythmia adult superpanels\r\n- additional findings adult panel, minus STK11, MUTYH, BTD, OTC, GAA, RPE65\r\n- AD nonsyndromic monogenic diabetes genes\r\n- dyslipidaemia\r\n- osteogenesis imperfecta\r\n- bleeding & platelet disorders\r\n- melanoma",
                "status": "public",
                "version": "0.21",
                "version_created": "2026-01-16T12:00:12.269232+11:00",
                "relevant_disorders": [],
                "stats": {
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                    "number_of_strs": 0,
                    "number_of_regions": 0
                },
                "types": [
                    {
                        "name": "Melbourne Genomics",
                        "slug": "melbourne-genomics",
                        "description": "Panel used by a Melbourne Genomics project."
                    },
                    {
                        "name": "Royal Melbourne Hospital",
                        "slug": "royal-melbourne-hospital",
                        "description": "Royal Melbourne Hospital"
                    }
                ],
                "child_panel_ids": []
            },
            "transcript": null
        },
        {
            "gene_data": {
                "alias": [
                    "VHL1"
                ],
                "biotype": "protein_coding",
                "hgnc_id": "HGNC:12687",
                "gene_name": "von Hippel-Lindau tumor suppressor",
                "omim_gene": [
                    "608537"
                ],
                "alias_name": null,
                "gene_symbol": "VHL",
                "hgnc_symbol": "VHL",
                "hgnc_release": "2017-11-03",
                "ensembl_genes": {
                    "GRch37": {
                        "82": {
                            "location": "3:10182692-10193904",
                            "ensembl_id": "ENSG00000134086"
                        }
                    },
                    "GRch38": {
                        "90": {
                            "location": "3:10141008-10152220",
                            "ensembl_id": "ENSG00000134086"
                        }
                    }
                },
                "hgnc_date_symbol_changed": "1986-01-01"
            },
            "entity_type": "gene",
            "entity_name": "VHL",
            "confidence_level": "3",
            "penetrance": null,
            "mode_of_pathogenicity": "",
            "publications": [],
            "evidence": [
                "Expert Review Green",
                "Melbourne Genomics Health Alliance"
            ],
            "phenotypes": [
                "von Hippel-Lindau syndrome , MIM#193300"
            ],
            "mode_of_inheritance": "MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted",
            "tags": [],
            "panel": {
                "id": 4126,
                "hash_id": null,
                "name": "Transplant Co-Morbidity",
                "disease_group": "Screening",
                "disease_sub_group": "",
                "description": "This panel was built for the Melbourne Genomics Health Alliance Transplant Clinical Change Project. It contains genes from the following panels, that may be actionable in the study cohort:\r\n- cardiomyopathy and arrhythmia adult superpanels\r\n- additional findings adult panel, minus STK11, MUTYH, BTD, OTC, GAA, RPE65\r\n- AD nonsyndromic monogenic diabetes genes\r\n- dyslipidaemia\r\n- osteogenesis imperfecta\r\n- bleeding & platelet disorders\r\n- melanoma",
                "status": "public",
                "version": "0.21",
                "version_created": "2026-01-16T12:00:12.269232+11:00",
                "relevant_disorders": [],
                "stats": {
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                    "number_of_strs": 0,
                    "number_of_regions": 0
                },
                "types": [
                    {
                        "name": "Melbourne Genomics",
                        "slug": "melbourne-genomics",
                        "description": "Panel used by a Melbourne Genomics project."
                    },
                    {
                        "name": "Royal Melbourne Hospital",
                        "slug": "royal-melbourne-hospital",
                        "description": "Royal Melbourne Hospital"
                    }
                ],
                "child_panel_ids": []
            },
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                        "name": "Royal Melbourne Hospital",
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        {
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                "child_panel_ids": []
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        },
        {
            "gene_data": {
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        {
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                "biotype": "protein_coding",
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                "hgnc_date_symbol_changed": "1986-01-01"
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        {
            "gene_data": {
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        {
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                        "description": "Royal Melbourne Hospital"
                    }
                ],
                "child_panel_ids": []
            },
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        },
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                    "CMH7"
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                "hgnc_id": "HGNC:11947",
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                    "GRch37": {
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                "hgnc_date_symbol_changed": "1989-12-11"
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                "2226790",
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                "Victorian Clinical Genetics Services"
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                "version_created": "2026-01-16T12:00:12.269232+11:00",
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                        "name": "Melbourne Genomics",
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                        "name": "Royal Melbourne Hospital",
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                ],
                "child_panel_ids": []
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        },
        {
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                "biotype": "protein_coding",
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                        "name": "Royal Melbourne Hospital",
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                ],
                "child_panel_ids": []
            },
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        },
        {
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                    "DKFZp586G1919",
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                "biotype": "protein_coding",
                "hgnc_id": "HGNC:28472",
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                "alias_name": null,
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                "Victorian Clinical Genetics Services"
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            "panel": {
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                "child_panel_ids": []
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        {
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                "hgnc_id": "HGNC:25535",
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                    "611236"
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                "hgnc_date_symbol_changed": "2004-12-22"
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                "child_panel_ids": []
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        {
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                "biotype": "protein_coding",
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                "Expert list",
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        {
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                "child_panel_ids": []
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        {
            "gene_data": {
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        {
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                        "name": "Royal Melbourne Hospital",
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                ],
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                        "name": "Melbourne Genomics",
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                        "name": "Royal Melbourne Hospital",
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        {
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                        "name": "Royal Melbourne Hospital",
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                "child_panel_ids": []
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        {
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                    "600993"
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                "Expert Review Green",
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        {
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            "panel": {
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                "child_panel_ids": []
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        {
            "gene_data": {
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                "hgnc_date_symbol_changed": "2006-04-05"
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            "panel": {
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                "child_panel_ids": []
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        {
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                "Expert Review Green",
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        {
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                    "SMS2"
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                "32028018",
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                ],
                "child_panel_ids": []
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        {
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                "alias": [
                    "HSP47",
                    "colligen"
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                    "collagen binding protein 1"
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                "Expert Review Green",
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                "child_panel_ids": []
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        {
            "gene_data": {
                "alias": [
                    "API",
                    "ALPHA-2-PI",
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                "biotype": "protein_coding",
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                "omim_gene": [
                    "613168"
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                "alias_name": [
                    "alpha-2-plasmin inhibitor",
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            "panel": {
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                "child_panel_ids": []
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        {
            "gene_data": {
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                "biotype": "protein_coding",
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                "omim_gene": [
                    "172860"
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                "alias_name": [
                    "pigment epithelium-derived factor",
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                "gene_symbol": "SERPINF1",
                "hgnc_symbol": "SERPINF1",
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                "ensembl_genes": {
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            "entity_type": "gene",
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                "Expert Review Green",
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                ],
                "child_panel_ids": []
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        {
            "gene_data": {
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                    },
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        {
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                "biotype": "protein_coding",
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}