Gene Search List
Search Genes
GET /api/v1/genes/?format=api&page=3
https://panelapp.genomicsengland.co.uk/api/v1/genes/?format=api&page=4", "previous": "https://panelapp.genomicsengland.co.uk/api/v1/genes/?format=api&page=2", "results": [ { "gene_data": { "alias": [ "CDC25L", "CDC25", "GRF55", "H-GRF55", "GNRP", "PP13187" ], "biotype": "protein_coding", "hgnc_id": "HGNC:9875", "gene_name": "Ras protein specific guanine nucleotide releasing factor 1", "omim_gene": [ "606600" ], "alias_name": null, "gene_symbol": "RASGRF1", "hgnc_symbol": "RASGRF1", "hgnc_release": "2017-11-03", "ensembl_genes": { "GRch37": { "82": { "location": "15:79252289-79383115", "ensembl_id": "ENSG00000058335" } }, "GRch38": { "90": { "location": "15:78959947-79090773", "ensembl_id": "ENSG00000058335" } } }, "hgnc_date_symbol_changed": "1994-02-11" }, "entity_type": "gene", "entity_name": "RASGRF1", "confidence_level": "1", "penetrance": null, "mode_of_pathogenicity": "", "publications": [ "30794780", "26769960" ], "evidence": [ "Literature" ], "phenotypes": [], 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"location": "15:75727670-75738623", "ensembl_id": "ENSG00000246877" } } }, "hgnc_date_symbol_changed": "2008-10-24" }, "entity_type": "gene", "entity_name": "DNM1P35", "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": [], "biotype": "protein_coding", "hgnc_id": "HGNC:10485", "gene_name": "ryanodine receptor 3", "omim_gene": [ "180903" ], "alias_name": null, "gene_symbol": "RYR3", "hgnc_symbol": "RYR3", "hgnc_release": "2017-11-03", "ensembl_genes": { "GRch37": { "82": { "location": "15:33603163-34158303", "ensembl_id": "ENSG00000198838" } }, "GRch38": { "90": { "location": "15:33310945-33866121", "ensembl_id": "ENSG00000198838" } } }, "hgnc_date_symbol_changed": "1993-05-12" }, "entity_type": "gene", "entity_name": "RYR3", "confidence_level": "1", "penetrance": null, "mode_of_pathogenicity": "", "publications": [ "27835649", "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", "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": [ "NCRNA00214", "UBE3A-AS" ], "biotype": "processed_transcript", "hgnc_id": "HGNC:37462", "gene_name": "small nucleolar RNA host gene 14", "omim_gene": [ "616259" ], "alias_name": [ "non-protein coding RNA 214" ], "gene_symbol": "SNHG14", "hgnc_symbol": "SNHG14", "hgnc_release": "2017-11-03", "ensembl_genes": { "GRch37": { "82": { "location": "15:25223730-25664609", "ensembl_id": "ENSG00000224078" } }, "GRch38": { "90": { "location": "15:24978583-25419462", "ensembl_id": "ENSG00000224078" } } }, "hgnc_date_symbol_changed": "2011-08-22" }, "entity_type": "gene", "entity_name": "SNHG14", "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, 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": [ "NCRNA00198" ], "biotype": "lincRNA", "hgnc_id": "HGNC:33235", "gene_name": "Prader-Willi region non-protein coding RNA 1", "omim_gene": [ "611215" ], "alias_name": [ "non-protein coding RNA 198" ], "gene_symbol": "PWRN1", "hgnc_symbol": "PWRN1", "hgnc_release": "2017-11-03", "ensembl_genes": { "GRch37": { "82": { "location": "15:24738284-24897277", "ensembl_id": "ENSG00000259905" } }, "GRch38": { "90": { "location": "15:24493137-24652130", "ensembl_id": "ENSG00000259905" } } }, "hgnc_date_symbol_changed": "2007-01-04" }, "entity_type": "gene", "entity_name": "PWRN1", "confidence_level": "1", "penetrance": null, "mode_of_pathogenicity": "", "publications": [ "http://igc.otago.ac.nz/home.html", "30794780", "25953952" ], "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": [ "AS", "ANCR", "E6-AP", "FLJ26981" ], "biotype": "protein_coding", "hgnc_id": "HGNC:12496", "gene_name": "ubiquitin protein ligase E3A", "omim_gene": [ "601623" ], "alias_name": [ "Angelman syndrome" ], "gene_symbol": "UBE3A", "hgnc_symbol": "UBE3A", "hgnc_release": "2017-11-03T00:00:00", "ensembl_genes": { "GRch37": { "82": { "location": "15:25582381-25684128", "ensembl_id": "ENSG00000114062" } }, "GRch38": { "90": { "location": "15:25333728-25439056", "ensembl_id": "ENSG00000114062" } } }, "hgnc_date_symbol_changed": "1993-10-21" }, "entity_type": "gene", "entity_name": "UBE3A", "confidence_level": "3", "penetrance": "Complete", "mode_of_pathogenicity": "", "publications": [ "21974935", "18500341]", "2309780", "PMID: 9887341", "30794780", "12545427", "[7795645", "8988171", "http://igc.otago.ac.nz/home.html", "8988172" ], "evidence": [ "Literature", "Expert Review Green", "Imprinting GeCIP Subdomain" ], "phenotypes": [ "Phenotype resulting from under expression: Angelman Syndrome", "Affected tissue: brain" ], "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 for research." } ] }, "transcript": null }, { "gene_data": { "alias": [ "HBII-438b" ], "biotype": "snoRNA", "hgnc_id": "HGNC:32774", "gene_name": "small nucleolar RNA, C/D box 109B", "omim_gene": null, "alias_name": null, "gene_symbol": "SNORD109B", "hgnc_symbol": "SNORD109B", 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"number_of_regions": 0 }, "types": [ { "name": "Research", "slug": "research", "description": "This is a gene panel used for research." } ] }, "transcript": null }, { "gene_data": { "alias": [ "HBII-52-1" ], "biotype": "snoRNA", "hgnc_id": "HGNC:33020", "gene_name": "small nucleolar RNA, C/D box 115-1", "omim_gene": [ "609837" ], "alias_name": null, "gene_symbol": "SNORD115-1", "hgnc_symbol": "SNORD115-1", "hgnc_release": "2017-11-03", "ensembl_genes": { "GRch37": { "82": { "location": "15:25415870-25415951", "ensembl_id": "ENSG00000201831" } }, "GRch38": { "90": { "location": "15:25170723-25170804", "ensembl_id": "ENSG00000201831" } } }, "hgnc_date_symbol_changed": "2007-02-15" }, "entity_type": "gene", "entity_name": "SNORD115-1", "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, 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"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": [ "HBII-437" ], "biotype": "snoRNA", "hgnc_id": "HGNC:32772", "gene_name": "small nucleolar RNA, C/D box 108", "omim_gene": null, "alias_name": null, "gene_symbol": "SNORD108", "hgnc_symbol": "SNORD108", "hgnc_release": "2017-11-03", "ensembl_genes": { "GRch37": { "82": { "location": "15:25232072-25232142", "ensembl_id": "ENSG00000239014" } }, "GRch38": { "90": { "location": "15:24986925-24986995", "ensembl_id": "ENSG00000239014" } } }, "hgnc_date_symbol_changed": "2006-05-08" }, "entity_type": "gene", "entity_name": "SNORD108", "confidence_level": "1", "penetrance": null, "mode_of_pathogenicity": "", "publications": [ "30794780", "http://igc.otago.ac.nz/home.html" ], "evidence": [ "Literature" ], "phenotypes": [], "mode_of_inheritance": 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null, "gene_symbol": "SNORD107", "hgnc_symbol": "SNORD107", "hgnc_release": "2017-11-03", "ensembl_genes": {}, "hgnc_date_symbol_changed": "2006-05-08" }, "entity_type": "gene", "entity_name": "SNORD107", "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, maternally imprinted (paternal allele expressed)", "tags": [ "locus-type-rna-small-nuclear", "ensembl_ids_known_missing" ], "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 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