{"count":1,"next":null,"previous":null,"results":[{"gene_data":{"alias":[],"biotype":"protein_coding","hgnc_id":"HGNC:8794","gene_name":"phosphodiesterase 8B","omim_gene":["603390"],"alias_name":null,"gene_symbol":"PDE8B","hgnc_symbol":"PDE8B","hgnc_release":"2017-11-03","ensembl_genes":{"GRch37":{"82":{"location":"5:76506274-76725632","ensembl_id":"ENSG00000113231"}},"GRch38":{"90":{"location":"5:77210449-77429807","ensembl_id":"ENSG00000113231"}}},"hgnc_date_symbol_changed":"1998-11-30"},"entity_type":"gene","entity_name":"PDE8B","confidence_level":"3","penetrance":null,"mode_of_pathogenicity":"","publications":["18272904"],"evidence":["Expert Review Green","NHS GMS"],"phenotypes":["Pigmented nodular adrenocortical disease, primary, 3, 614190"],"mode_of_inheritance":"MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted","tags":[],"panel":{"id":566,"hash_id":null,"name":"Primary pigmented nodular adrenocortical disease","disease_group":"","disease_sub_group":"","status":"public","version":"1.0","version_created":"2019-07-31T14:33:58.646299Z","relevant_disorders":["R160"],"stats":{"number_of_genes":4,"number_of_strs":0,"number_of_regions":0},"types":[{"name":"GMS Rare Disease","slug":"gms-rare-disease","description":"This panel type is used for GMS panels that are not virtual (i.e. could be a wet lab test)"},{"name":"GMS signed-off","slug":"gms-signed-off","description":"This panel has undergone review by a NHSE GMS disease specialist group and processes to be signed-off for use within the GMS."}]}}]}