{"count":1,"next":null,"previous":null,"results":[{"gene_data":{"alias":["hTAFII68","RBP56","Npl3"],"biotype":null,"hgnc_id":"HGNC:11547","gene_name":"TATA-box binding protein associated factor 15","omim_gene":["601574"],"alias_name":null,"gene_symbol":"TAF15","hgnc_symbol":"TAF15","hgnc_release":"2017-11-03","ensembl_genes":{"GRch37":{"82":{"location":"17:34136459-34191619","ensembl_id":"ENSG00000172660"}},"GRch38":{"90":{"location":"17:35713791-35864615","ensembl_id":"ENSG00000270647"}}},"hgnc_date_symbol_changed":"2001-12-07"},"entity_type":"gene","entity_name":"TAF15","confidence_level":"1","penetrance":null,"mode_of_pathogenicity":"","publications":["22065782","26601740"],"evidence":["Expert Review Red","NHS GMS","Yorkshire and North East GLH"],"phenotypes":["Amyotrophic lateral sclerosis"],"mode_of_inheritance":"MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown","tags":[],"panel":{"id":474,"hash_id":null,"name":"Neurodegenerative disorders - adult onset","disease_group":"","disease_sub_group":"","status":"public","version":"1.106","version_created":"2019-09-20T16:19:10.101841Z","relevant_disorders":["R58"],"stats":{"number_of_genes":395,"number_of_strs":18,"number_of_regions":4},"types":[{"name":"GMS Rare Disease Virtual","slug":"gms-rare-disease-virtual","description":"This is a panel for the Genomic Medicine Service for an exome/genome/panel based test that requires a virtual gene panel for rare disease in the Test Directory."}]}}]}