Search Genes

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                "alias": [
                    "iGNT",
                    "iGAT",
                    "iGnT",
                    "BETA3GNTI",
                    "B3GN-T1"
                ],
                "biotype": "protein_coding",
                "hgnc_id": "HGNC:15685",
                "gene_name": "beta-1,4-glucuronyltransferase 1",
                "omim_gene": [
                    "605517"
                ],
                "alias_name": [
                    "N-acetyllactosaminide beta-1,3-N-acetylglucosaminyltransferase"
                ],
                "gene_symbol": "B4GAT1",
                "hgnc_symbol": "B4GAT1",
                "hgnc_release": "2017-11-03",
                "ensembl_genes": {
                    "GRch37": {
                        "82": {
                            "location": "11:66112843-66115163",
                            "ensembl_id": "ENSG00000174684"
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                    },
                    "GRch38": {
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                            "location": "11:66345372-66347692",
                            "ensembl_id": "ENSG00000174684"
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                },
                "hgnc_date_symbol_changed": "2014-12-17"
            },
            "entity_type": "gene",
            "entity_name": "B4GAT1",
            "confidence_level": "1",
            "penetrance": null,
            "mode_of_pathogenicity": "",
            "publications": [
                "23359570",
                "23877401",
                "23359570",
                "23217742"
            ],
            "evidence": [
                "Expert Review Red",
                "Victorian Clinical Genetics Services"
            ],
            "phenotypes": [
                "Muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies), type A, 13 MIM# 615287"
            ],
            "mode_of_inheritance": "BIALLELIC, autosomal or pseudoautosomal",
            "tags": [],
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                "id": 47,
                "hash_id": null,
                "name": "Arthrogryposis",
                "disease_group": "Neurology and neurodevelopmental disorders",
                "disease_sub_group": "",
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                "status": "public",
                "version": "1.19",
                "version_created": "2026-04-02T19:32:17.814766+11:00",
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                    "Flexion contracture",
                    "HP:0001371"
                ],
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                    {
                        "name": "Victorian Clinical Genetics Services",
                        "slug": "victorian-clinical-genetics-services",
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                    {
                        "name": "Rare Disease",
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                        "description": "Rare disease panels"
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                        "name": "Royal Melbourne Hospital",
                        "slug": "royal-melbourne-hospital",
                        "description": "Royal Melbourne Hospital"
                    }
                ],
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            "transcript": null
        },
        {
            "gene_data": {
                "alias": [
                    "LAP1B",
                    "FLJ13142"
                ],
                "biotype": "protein_coding",
                "hgnc_id": "HGNC:29456",
                "gene_name": "torsin 1A interacting protein 1",
                "omim_gene": [
                    "614512"
                ],
                "alias_name": [
                    "lamina associated polypeptide 1B"
                ],
                "gene_symbol": "TOR1AIP1",
                "hgnc_symbol": "TOR1AIP1",
                "hgnc_release": "2017-11-03",
                "ensembl_genes": {
                    "GRch37": {
                        "82": {
                            "location": "1:179851177-179894135",
                            "ensembl_id": "ENSG00000143337"
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                    },
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                        "90": {
                            "location": "1:179882042-179925000",
                            "ensembl_id": "ENSG00000143337"
                        }
                    }
                },
                "hgnc_date_symbol_changed": "2005-06-07"
            },
            "entity_type": "gene",
            "entity_name": "TOR1AIP1",
            "confidence_level": "3",
            "penetrance": null,
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            "publications": [
                "24856141",
                "31299614",
                "30723199",
                "27342937",
                "32055997"
            ],
            "evidence": [
                "Expert Review Green",
                "Literature"
            ],
            "phenotypes": [
                "Muscular dystrophy, autosomal recessive, with rigid spine and distal joint contractures MIM#617072",
                "Progeroid appearance",
                "Cataracts",
                "Microcephaly",
                "Deafness",
                "Contractures"
            ],
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            "tags": [],
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                "id": 47,
                "hash_id": null,
                "name": "Arthrogryposis",
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                    "Flexion contracture",
                    "HP:0001371"
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                        "name": "Victorian Clinical Genetics Services",
                        "slug": "victorian-clinical-genetics-services",
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                        "name": "Rare Disease",
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                        "slug": "royal-melbourne-hospital",
                        "description": "Royal Melbourne Hospital"
                    }
                ],
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        {
            "gene_data": {
                "alias": [
                    "FLJ20297",
                    "FLJ20756",
                    "nSMase-3",
                    "KIAA1418",
                    "NSMASE3",
                    "NET13"
                ],
                "biotype": "protein_coding",
                "hgnc_id": "HGNC:32949",
                "gene_name": "sphingomyelin phosphodiesterase 4",
                "omim_gene": [
                    "610457"
                ],
                "alias_name": [
                    "neutral sphingomyelinase-3"
                ],
                "gene_symbol": "SMPD4",
                "hgnc_symbol": "SMPD4",
                "hgnc_release": "2017-11-03",
                "ensembl_genes": {
                    "GRch37": {
                        "82": {
                            "location": "2:130908981-130940323",
                            "ensembl_id": "ENSG00000136699"
                        }
                    },
                    "GRch38": {
                        "90": {
                            "location": "2:130151392-130182750",
                            "ensembl_id": "ENSG00000136699"
                        }
                    }
                },
                "hgnc_date_symbol_changed": "2006-07-12"
            },
            "entity_type": "gene",
            "entity_name": "SMPD4",
            "confidence_level": "3",
            "penetrance": null,
            "mode_of_pathogenicity": null,
            "publications": [
                "31495489"
            ],
            "evidence": [
                "Expert Review Green",
                "Literature"
            ],
            "phenotypes": [
                "Microcephaly",
                "congenital arthrogryposis, intellectual disability"
            ],
            "mode_of_inheritance": "BIALLELIC, autosomal or pseudoautosomal",
            "tags": [],
            "panel": {
                "id": 47,
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                "name": "Arthrogryposis",
                "disease_group": "Neurology and neurodevelopmental disorders",
                "disease_sub_group": "",
                "description": "This panel contains genes that have been associated with multiple congenital contractures (arthrogryposis). Primary genetic aetiologies include neuropathic processes; myopathic processes; end-plate abnormalities; and syndromic/metabolic disorders that affect the movement of the developing embryo/fetus.\r\n\r\nThis panel has been compared against the Genomics England PanelApp 'Arthrogryposis' panel with all discrepancies resolved, and reciprocal feedback provided to Genomics England, 1/8/2020.\r\n\r\nUpdated following literature review 25/11/2025.",
                "status": "public",
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                "version_created": "2026-04-02T19:32:17.814766+11:00",
                "relevant_disorders": [
                    "Flexion contracture",
                    "HP:0001371"
                ],
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                    {
                        "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": []
        },
        {
            "gene_data": {
                "alias": [
                    "B3GNT-2",
                    "BETA3GNT",
                    "B3GN-T2",
                    "B3GN-T1"
                ],
                "biotype": "protein_coding",
                "hgnc_id": "HGNC:15629",
                "gene_name": "UDP-GlcNAc:betaGal beta-1,3-N-acetylglucosaminyltransferase 2",
                "omim_gene": [
                    "605581"
                ],
                "alias_name": null,
                "gene_symbol": "B3GNT2",
                "hgnc_symbol": "B3GNT2",
                "hgnc_release": "2017-11-03",
                "ensembl_genes": {
                    "GRch37": {
                        "82": {
                            "location": "2:62423248-62451866",
                            "ensembl_id": "ENSG00000170340"
                        }
                    },
                    "GRch38": {
                        "90": {
                            "location": "2:62196113-62224731",
                            "ensembl_id": "ENSG00000170340"
                        }
                    }
                },
                "hgnc_date_symbol_changed": "2006-04-12"
            },
            "entity_type": "gene",
            "entity_name": "B3GNT2",
            "confidence_level": "1",
            "penetrance": null,
            "mode_of_pathogenicity": "",
            "publications": [
                "23359570",
                "23877401"
            ],
            "evidence": [
                "Expert Review Red",
                "Victorian Clinical Genetics Services"
            ],
            "phenotypes": [
                "Muscular dystrophy-dystroglycanopathy"
            ],
            "mode_of_inheritance": "BIALLELIC, autosomal or pseudoautosomal",
            "tags": [],
            "panel": {
                "id": 47,
                "hash_id": null,
                "name": "Arthrogryposis",
                "disease_group": "Neurology and neurodevelopmental disorders",
                "disease_sub_group": "",
                "description": "This panel contains genes that have been associated with multiple congenital contractures (arthrogryposis). Primary genetic aetiologies include neuropathic processes; myopathic processes; end-plate abnormalities; and syndromic/metabolic disorders that affect the movement of the developing embryo/fetus.\r\n\r\nThis panel has been compared against the Genomics England PanelApp 'Arthrogryposis' panel with all discrepancies resolved, and reciprocal feedback provided to Genomics England, 1/8/2020.\r\n\r\nUpdated following literature review 25/11/2025.",
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                "version": "1.19",
                "version_created": "2026-04-02T19:32:17.814766+11:00",
                "relevant_disorders": [
                    "Flexion contracture",
                    "HP:0001371"
                ],
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                    "number_of_strs": 0,
                    "number_of_regions": 0
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                    {
                        "name": "Victorian Clinical Genetics Services",
                        "slug": "victorian-clinical-genetics-services",
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                    },
                    {
                        "name": "Rare Disease",
                        "slug": "rare-disease",
                        "description": "Rare disease panels"
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                    {
                        "name": "Royal Melbourne Hospital",
                        "slug": "royal-melbourne-hospital",
                        "description": "Royal Melbourne Hospital"
                    }
                ],
                "child_panel_ids": []
            },
            "transcript": null
        },
        {
            "gene_data": {
                "alias": [
                    "SIGMA1B"
                ],
                "biotype": "protein_coding",
                "hgnc_id": "HGNC:560",
                "gene_name": "adaptor related protein complex 1 sigma 2 subunit",
                "omim_gene": [
                    "300629"
                ],
                "alias_name": null,
                "gene_symbol": "AP1S2",
                "hgnc_symbol": "AP1S2",
                "hgnc_release": "2017-11-03",
                "ensembl_genes": {
                    "GRch37": {
                        "82": {
                            "location": "X:15843929-15873054",
                            "ensembl_id": "ENSG00000182287"
                        }
                    },
                    "GRch38": {
                        "90": {
                            "location": "X:15825806-15854931",
                            "ensembl_id": "ENSG00000182287"
                        }
                    }
                },
                "hgnc_date_symbol_changed": "2000-09-01"
            },
            "entity_type": "gene",
            "entity_name": "AP1S2",
            "confidence_level": "1",
            "penetrance": null,
            "mode_of_pathogenicity": "",
            "publications": [
                "30714330"
            ],
            "evidence": [
                "Expert Review Red",
                "Victorian Clinical Genetics Services"
            ],
            "phenotypes": [
                "Pettigrew syndrome, MIM# 304340"
            ],
            "mode_of_inheritance": "X-LINKED: hemizygous mutation in males, biallelic mutations in females",
            "tags": [],
            "panel": {
                "id": 47,
                "hash_id": null,
                "name": "Arthrogryposis",
                "disease_group": "Neurology and neurodevelopmental disorders",
                "disease_sub_group": "",
                "description": "This panel contains genes that have been associated with multiple congenital contractures (arthrogryposis). Primary genetic aetiologies include neuropathic processes; myopathic processes; end-plate abnormalities; and syndromic/metabolic disorders that affect the movement of the developing embryo/fetus.\r\n\r\nThis panel has been compared against the Genomics England PanelApp 'Arthrogryposis' panel with all discrepancies resolved, and reciprocal feedback provided to Genomics England, 1/8/2020.\r\n\r\nUpdated following literature review 25/11/2025.",
                "status": "public",
                "version": "1.19",
                "version_created": "2026-04-02T19:32:17.814766+11:00",
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                    "HP:0001371"
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                    "number_of_regions": 0
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                "types": [
                    {
                        "name": "Victorian Clinical Genetics Services",
                        "slug": "victorian-clinical-genetics-services",
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                    {
                        "name": "Rare Disease",
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                        "name": "Royal Melbourne Hospital",
                        "slug": "royal-melbourne-hospital",
                        "description": "Royal Melbourne Hospital"
                    }
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        },
        {
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                "alias": [
                    "ISSX",
                    "CT121",
                    "EIEE1"
                ],
                "biotype": "protein_coding",
                "hgnc_id": "HGNC:18060",
                "gene_name": "aristaless related homeobox",
                "omim_gene": [
                    "300382"
                ],
                "alias_name": [
                    "cancer/testis antigen 121"
                ],
                "gene_symbol": "ARX",
                "hgnc_symbol": "ARX",
                "hgnc_release": "2017-11-03",
                "ensembl_genes": {
                    "GRch37": {
                        "82": {
                            "location": "X:25021811-25034065",
                            "ensembl_id": "ENSG00000004848"
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                    },
                    "GRch38": {
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                            "location": "X:25003694-25016420",
                            "ensembl_id": "ENSG00000004848"
                        }
                    }
                },
                "hgnc_date_symbol_changed": "2002-02-11"
            },
            "entity_type": "gene",
            "entity_name": "ARX",
            "confidence_level": "2",
            "penetrance": null,
            "mode_of_pathogenicity": "",
            "publications": [
                "21416597"
            ],
            "evidence": [
                "Expert Review Amber",
                "Victorian Clinical Genetics Services"
            ],
            "phenotypes": [
                "Epileptic encephalopathy, early infantile, 1 308350",
                "Hydranencephaly with abnormal genitalia 300215",
                "Lissencephaly, X-linked 2 300215",
                "Mental retardation, X-linked 29 and others 300419",
                "Partington syndrome 309510",
                "Proud syndrome 300004"
            ],
            "mode_of_inheritance": "X-LINKED: hemizygous mutation in males, biallelic mutations in females",
            "tags": [],
            "panel": {
                "id": 47,
                "hash_id": null,
                "name": "Arthrogryposis",
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                "description": "This panel contains genes that have been associated with multiple congenital contractures (arthrogryposis). Primary genetic aetiologies include neuropathic processes; myopathic processes; end-plate abnormalities; and syndromic/metabolic disorders that affect the movement of the developing embryo/fetus.\r\n\r\nThis panel has been compared against the Genomics England PanelApp 'Arthrogryposis' panel with all discrepancies resolved, and reciprocal feedback provided to Genomics England, 1/8/2020.\r\n\r\nUpdated following literature review 25/11/2025.",
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                "version_created": "2026-04-02T19:32:17.814766+11:00",
                "relevant_disorders": [
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                    "HP:0001371"
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                    "number_of_regions": 0
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                    {
                        "name": "Victorian Clinical Genetics Services",
                        "slug": "victorian-clinical-genetics-services",
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                        "name": "Rare Disease",
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                        "slug": "royal-melbourne-hospital",
                        "description": "Royal Melbourne Hospital"
                    }
                ],
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            },
            "transcript": null
        },
        {
            "gene_data": {
                "alias": [
                    "MGC39558"
                ],
                "biotype": "protein_coding",
                "hgnc_id": "HGNC:28596",
                "gene_name": "beta-1,3-N-acetylgalactosaminyltransferase 2",
                "omim_gene": [
                    "610194"
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                "alias_name": null,
                "gene_symbol": "B3GALNT2",
                "hgnc_symbol": "B3GALNT2",
                "hgnc_release": "2017-11-03",
                "ensembl_genes": {
                    "GRch37": {
                        "82": {
                            "location": "1:235613238-235667781",
                            "ensembl_id": "ENSG00000162885"
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                    "GRch38": {
                        "90": {
                            "location": "1:235449923-235504481",
                            "ensembl_id": "ENSG00000162885"
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                    }
                },
                "hgnc_date_symbol_changed": "2005-02-10"
            },
            "entity_type": "gene",
            "entity_name": "B3GALNT2",
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                "Victorian Clinical Genetics Services"
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                "Muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies, type A, 11, MIM# 615181"
            ],
            "mode_of_inheritance": "Unknown",
            "tags": [],
            "panel": {
                "id": 47,
                "hash_id": null,
                "name": "Arthrogryposis",
                "disease_group": "Neurology and neurodevelopmental disorders",
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                "description": "This panel contains genes that have been associated with multiple congenital contractures (arthrogryposis). Primary genetic aetiologies include neuropathic processes; myopathic processes; end-plate abnormalities; and syndromic/metabolic disorders that affect the movement of the developing embryo/fetus.\r\n\r\nThis panel has been compared against the Genomics England PanelApp 'Arthrogryposis' panel with all discrepancies resolved, and reciprocal feedback provided to Genomics England, 1/8/2020.\r\n\r\nUpdated following literature review 25/11/2025.",
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                "version_created": "2026-04-02T19:32:17.814766+11:00",
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                    "Flexion contracture",
                    "HP:0001371"
                ],
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                "types": [
                    {
                        "name": "Victorian Clinical Genetics Services",
                        "slug": "victorian-clinical-genetics-services",
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                    {
                        "name": "Rare Disease",
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                        "description": "Rare disease panels"
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                        "name": "Royal Melbourne Hospital",
                        "slug": "royal-melbourne-hospital",
                        "description": "Royal Melbourne Hospital"
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        },
        {
            "gene_data": {
                "alias": [
                    "XH2",
                    "XNP"
                ],
                "biotype": "protein_coding",
                "hgnc_id": "HGNC:886",
                "gene_name": "ATRX, chromatin remodeler",
                "omim_gene": [
                    "300032",
                    "300504"
                ],
                "alias_name": [
                    "RAD54 homolog (S. cerevisiae)"
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                "hgnc_symbol": "ATRX",
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                "ensembl_genes": {
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                        "82": {
                            "location": "X:76760356-77041702",
                            "ensembl_id": "ENSG00000085224"
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                            "location": "X:77504878-77786269",
                            "ensembl_id": "ENSG00000085224"
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                "20301622"
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                "Expert Review Amber",
                "Victorian Clinical Genetics Services"
            ],
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                "Alpha-thalassemia/mental retardation syndrome, MIM# 301040"
            ],
            "mode_of_inheritance": "X-LINKED: hemizygous mutation in males, biallelic mutations in females",
            "tags": [],
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                    {
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                    {
                        "name": "Rare Disease",
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                        "name": "Royal Melbourne Hospital",
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                        "name": "Royal Melbourne Hospital",
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        {
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