Gene Search List
Search Genes
GET /api/v1/genes/?format=api&page=49
{ "count": 35522, "next": "https://panelapp-aus.org/api/v1/genes/?format=api&page=50", "previous": "https://panelapp-aus.org/api/v1/genes/?format=api&page=48", "results": [ { "gene_data": { "alias": [ "PGT", "OATP2A1" ], "biotype": "protein_coding", "hgnc_id": "HGNC:10955", "gene_name": "solute carrier organic anion transporter family member 2A1", "omim_gene": [ "601460" ], "alias_name": null, "gene_symbol": "SLCO2A1", "hgnc_symbol": "SLCO2A1", "hgnc_release": "2017-11-03", "ensembl_genes": { "GRch37": { "82": { "location": "3:133651540-133771028", "ensembl_id": "ENSG00000174640" } }, "GRch38": { "90": { "location": "3:133932696-134052184", "ensembl_id": "ENSG00000174640" } } }, "hgnc_date_symbol_changed": "2003-11-26" }, "entity_type": "gene", "entity_name": "SLCO2A1", "confidence_level": "3", "penetrance": null, "mode_of_pathogenicity": null, "publications": [ "PMID: 29313109" ], "evidence": [ "Expert Review Green", "Literature" ], "phenotypes": [ "Inflammatory bowel disease, 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"HGNC:13273", "gene_name": "dual oxidase 2", "omim_gene": [ "606759" ], "alias_name": [ "dual oxidase-like domains 2", "nicotinamide adenine dinucleotide phosphate oxidase", "flavoprotein NADPH oxidase", "NADPH thyroid oxidase 2", "NADH/NADPH thyroid oxidase p138-tox", "NADPH oxidase/peroxidase DUOX2" ], "gene_symbol": "DUOX2", "hgnc_symbol": "DUOX2", "hgnc_release": "2017-11-03", "ensembl_genes": { "GRch37": { "82": { "location": "15:45384848-45406542", "ensembl_id": "ENSG00000140279" } }, "GRch38": { "90": { "location": "15:45092650-45114344", "ensembl_id": "ENSG00000140279" } } }, "hgnc_date_symbol_changed": "2000-11-09" }, "entity_type": "gene", "entity_name": "DUOX2", "confidence_level": "3", "penetrance": null, "mode_of_pathogenicity": null, "publications": [ "PMID: 35429653", "27373512", "26301257", "28683258" ], "evidence": [ "Expert Review Green", "Literature" ], "phenotypes": [ "Inflammatory bowel disease, MONDO:0005265, DUOX2-related" ], "mode_of_inheritance": "BIALLELIC, autosomal or pseudoautosomal", "tags": [], "panel": { "id": 123, "hash_id": null, "name": "Inflammatory bowel disease", "disease_group": "Gastroenterological disorders", "disease_sub_group": "", "description": "This panel was developed and is maintained by VCGS.", "status": "public", "version": "0.126", "version_created": "2025-10-16T15:50:33.114198+11:00", "relevant_disorders": [ "Gastrointestinal inflammation", "HP:0004386" ], "stats": { "number_of_genes": 85, "number_of_strs": 0, "number_of_regions": 0 }, "types": [ { "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" } ], "child_panel_ids": [] }, "transcript": null }, { "gene_data": { "alias": [ "NOH1", "NOH-1", "MOX1", "GP91-2" ], "biotype": "protein_coding", "hgnc_id": "HGNC:7889", "gene_name": "NADPH oxidase 1", "omim_gene": [ "300225" ], "alias_name": [ "mitogenic oxidase (pyridine nucleotide-dependent superoxide-generating)", "NADPH oxidase homolog-1", "NADPH oxidase 1 variant NOH-1L" ], "gene_symbol": "NOX1", "hgnc_symbol": "NOX1", "hgnc_release": "2017-11-03", "ensembl_genes": { "GRch37": { "82": { "location": "X:100098313-100129334", "ensembl_id": "ENSG00000007952" } }, "GRch38": { "90": { "location": "X:100843324-100874345", "ensembl_id": "ENSG00000007952" } } }, "hgnc_date_symbol_changed": "2000-03-24" }, "entity_type": "gene", "entity_name": "NOX1", "confidence_level": "2", "penetrance": null, "mode_of_pathogenicity": null, "publications": [ "PMID: 29091079", "32064493" ], "evidence": [ "Expert Review Amber", "Literature" ], "phenotypes": [ "Inflammatory bowel disease, MONDO:0005265, NOX1-related" ], "mode_of_inheritance": "X-LINKED: hemizygous mutation in males, biallelic mutations in females", "tags": [], "panel": { "id": 123, "hash_id": null, "name": "Inflammatory bowel disease", "disease_group": "Gastroenterological disorders", "disease_sub_group": "", "description": "This panel was developed and is maintained by VCGS.", "status": "public", "version": "0.126", "version_created": "2025-10-16T15:50:33.114198+11:00", "relevant_disorders": [ "Gastrointestinal inflammation", "HP:0004386" ], "stats": { "number_of_genes": 85, "number_of_strs": 0, "number_of_regions": 0 }, "types": [ { "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" } ], "child_panel_ids": [] }, "transcript": null }, { "gene_data": { "alias": [ "SEMP1", "ILVASC" ], "biotype": "protein_coding", "hgnc_id": "HGNC:2032", "gene_name": "claudin 1", "omim_gene": [ "603718" ], "alias_name": [ "senescence-associated epithelial membrane protein 1" ], "gene_symbol": "CLDN1", "hgnc_symbol": "CLDN1", "hgnc_release": "2017-11-03", "ensembl_genes": { "GRch37": { "82": { "location": "3:190023490-190040264", "ensembl_id": "ENSG00000163347" } }, "GRch38": { "90": { "location": "3:190305701-190322475", "ensembl_id": "ENSG00000163347" } } }, "hgnc_date_symbol_changed": "1998-11-19" }, "entity_type": "gene", "entity_name": "CLDN1", "confidence_level": "3", "penetrance": null, "mode_of_pathogenicity": null, "publications": [ "12164927", "11889141", "29146216" ], "evidence": [ "Expert Review Green", "Literature" ], "phenotypes": [ "Ichthyosis, leukocyte vacuoles, alopecia, and sclerosing cholangitis MIM#607626" ], "mode_of_inheritance": "BIALLELIC, autosomal or pseudoautosomal", "tags": [], "panel": { "id": 124, "hash_id": null, "name": "Ichthyosis and Porokeratosis", "disease_group": "Dermatological disorders", "disease_sub_group": "", "description": "This panel was developed and is maintained by VCGS and RMH. 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