Gene Search List
Search Genes
GET /api/v1/genes/?format=api&page=4
https://panelapp.genomicsengland.co.uk/api/v1/genes/?format=api&page=5", "previous": "https://panelapp.genomicsengland.co.uk/api/v1/genes/?format=api&page=3", "results": [ { "gene_data": { "alias": [ "LOC54932", "FLJ20433", "mut-7" ], "biotype": "protein_coding", "hgnc_id": "HGNC:26023", "gene_name": "exonuclease 3'-5' domain containing 3", "omim_gene": null, "alias_name": null, "gene_symbol": "EXD3", "hgnc_symbol": "EXD3", "hgnc_release": "2017-11-03", "ensembl_genes": { "GRch37": { "82": { "location": "9:140201348-140317714", "ensembl_id": "ENSG00000187609" } }, "GRch38": { "90": { "location": "9:137306896-137423262", "ensembl_id": "ENSG00000187609" } } }, "hgnc_date_symbol_changed": "2009-03-04" }, "entity_type": "gene", "entity_name": "EXD3", "confidence_level": "1", "penetrance": null, "mode_of_pathogenicity": "", "publications": [ "30794780", "26769960" ], "evidence": [ "Literature" ], "phenotypes": [], "mode_of_inheritance": "MONOALLELIC, autosomal or pseudoautosomal, maternally imprinted (paternal allele expressed)", "tags": [], "panel": { "id": 227, "hash_id": "590b12638f6203169828a560", "name": "Genomic imprinting", "disease_group": "", "disease_sub_group": "", "status": "public", "version": "0.149", "version_created": "2023-03-01T09:20:41.727370Z", "relevant_disorders": [], "stats": { "number_of_genes": 230, "number_of_strs": 0, "number_of_regions": 0 }, "types": [ { "name": "Research", "slug": "research", "description": "This is a gene panel used for research." } ] }, "transcript": null }, { "gene_data": { "alias": [ "DAP-2" ], "biotype": "protein_coding", "hgnc_id": "HGNC:2906", "gene_name": "DLG associated protein 2", "omim_gene": [ "605438" ], "alias_name": null, "gene_symbol": "DLGAP2", "hgnc_symbol": "DLGAP2", "hgnc_release": "2017-11-03", "ensembl_genes": { "GRch37": { "82": { "location": "8:1449532-1656642", "ensembl_id": "ENSG00000198010" } }, "GRch38": { "90": { "location": "8:737596-1708474", "ensembl_id": "ENSG00000198010" } } }, "hgnc_date_symbol_changed": "1999-02-23" }, "entity_type": "gene", "entity_name": "DLGAP2", "confidence_level": "1", "penetrance": null, "mode_of_pathogenicity": "", "publications": [ "30794780", "27835649", "http://igc.otago.ac.nz/home.html" ], "evidence": [ "Literature" ], "phenotypes": [], "mode_of_inheritance": "MONOALLELIC, autosomal or pseudoautosomal, maternally imprinted (paternal allele expressed)", "tags": [], "panel": { "id": 227, "hash_id": "590b12638f6203169828a560", "name": "Genomic imprinting", "disease_group": "", "disease_sub_group": "", "status": "public", "version": "0.149", "version_created": "2023-03-01T09:20:41.727370Z", "relevant_disorders": [], "stats": { "number_of_genes": 230, "number_of_strs": 0, "number_of_regions": 0 }, "types": [ { "name": "Research", "slug": "research", "description": "This is a gene panel used for research." } ] }, "transcript": null }, { "gene_data": { "alias": [ "KIAA0870" ], "biotype": "protein_coding", "hgnc_id": "HGNC:29134", "gene_name": "DENN domain containing 3", "omim_gene": [ "617503" ], "alias_name": null, "gene_symbol": "DENND3", "hgnc_symbol": "DENND3", "hgnc_release": "2017-11-03", "ensembl_genes": { "GRch37": { "82": { "location": "8:142127377-142205907", "ensembl_id": "ENSG00000105339" } }, "GRch38": { "90": { "location": "8:141117278-141195808", "ensembl_id": "ENSG00000105339" } } }, "hgnc_date_symbol_changed": "2005-08-17" }, "entity_type": "gene", "entity_name": "DENND3", "confidence_level": "1", "penetrance": null, "mode_of_pathogenicity": "", "publications": [ "30794780" ], "evidence": [ "Literature" ], "phenotypes": [], "mode_of_inheritance": "MONOALLELIC, autosomal or pseudoautosomal, maternally imprinted (paternal allele expressed)", "tags": [], "panel": { "id": 227, "hash_id": "590b12638f6203169828a560", "name": "Genomic imprinting", "disease_group": "", "disease_sub_group": "", "status": "public", "version": "0.149", "version_created": "2023-03-01T09:20:41.727370Z", 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"7:129932974-129964020", "ensembl_id": "ENSG00000128510" } }, "GRch38": { "90": { "location": "7:130293134-130324180", "ensembl_id": "ENSG00000128510" } } }, "hgnc_date_symbol_changed": "2001-05-24" }, "entity_type": "gene", "entity_name": "CPA4", "confidence_level": "1", "penetrance": null, "mode_of_pathogenicity": "", "publications": [ "30794780", "http://igc.otago.ac.nz/home.html" ], "evidence": [ "Literature" ], "phenotypes": [], "mode_of_inheritance": "MONOALLELIC, autosomal or pseudoautosomal, paternally imprinted (maternal allele expressed)", "tags": [], "panel": { "id": 227, "hash_id": "590b12638f6203169828a560", "name": "Genomic imprinting", "disease_group": "", "disease_sub_group": "", "status": "public", "version": "0.149", "version_created": "2023-03-01T09:20:41.727370Z", "relevant_disorders": [], "stats": { "number_of_genes": 230, "number_of_strs": 0, "number_of_regions": 0 }, "types": [ { "name": "Research", "slug": "research", "description": "This is a gene panel used 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"disease_sub_group": "", "status": "public", "version": "0.149", "version_created": "2023-03-01T09:20:41.727370Z", "relevant_disorders": [], "stats": { "number_of_genes": 230, "number_of_strs": 0, "number_of_regions": 0 }, "types": [ { "name": "Research", "slug": "research", "description": "This is a gene panel used for research." } ] }, "transcript": null }, { "gene_data": { "alias": [ "CTR" ], "biotype": "protein_coding", "hgnc_id": "HGNC:1440", "gene_name": "calcitonin receptor", "omim_gene": [ "114131" ], "alias_name": null, "gene_symbol": "CALCR", "hgnc_symbol": "CALCR", "hgnc_release": "2017-11-03", "ensembl_genes": { "GRch37": { "82": { "location": "7:93053799-93204042", "ensembl_id": "ENSG00000004948" } }, "GRch38": { "90": { "location": "7:93424487-93574730", "ensembl_id": "ENSG00000004948" } } }, "hgnc_date_symbol_changed": "1993-03-23" }, "entity_type": "gene", "entity_name": "CALCR", "confidence_level": "1", "penetrance": null, "mode_of_pathogenicity": "", "publications": [ 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