{"count":1,"next":null,"previous":null,"results":[{"gene_data":{"alias":["PUMH1","KIAA0099"],"biotype":"protein_coding","hgnc_id":"HGNC:14957","gene_name":"pumilio RNA binding family member 1","omim_gene":["607204"],"alias_name":null,"gene_symbol":"PUM1","hgnc_symbol":"PUM1","hgnc_release":"2017-11-03","ensembl_genes":{"GRch37":{"82":{"location":"1:31404353-31538838","ensembl_id":"ENSG00000134644"}},"GRch38":{"90":{"location":"1:30931506-31065991","ensembl_id":"ENSG00000134644"}}},"hgnc_date_symbol_changed":"2001-03-27"},"entity_type":"gene","entity_name":"PUM1","confidence_level":"3","penetrance":null,"mode_of_pathogenicity":"","publications":[],"evidence":["Expert Review Green","London North GLH","NHS GMS","Wessex and West Midlands GLH"],"phenotypes":["Spinocerebellar ataxia 47, 617931"],"mode_of_inheritance":"MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted","tags":[],"panel":{"id":466,"hash_id":null,"name":"Hereditary ataxia - adult onset","disease_group":"","disease_sub_group":"","status":"public","version":"1.211","version_created":"2019-09-20T14:18:40.957460Z","relevant_disorders":["Hereditary ataxia with onset in adulthood","R54"],"stats":{"number_of_genes":236,"number_of_strs":13,"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."}]}}]}