{"count":1,"next":null,"previous":null,"results":[{"gene_data":{"alias":[],"biotype":"protein_coding","hgnc_id":"HGNC:20731","gene_name":"G protein subunit beta 4","omim_gene":["610863"],"alias_name":["transducin beta chain 4"],"gene_symbol":"GNB4","hgnc_symbol":"GNB4","hgnc_release":"2017-11-03T00:00:00","ensembl_genes":{"GRch37":{"82":{"location":"3:179116990-179169378","ensembl_id":"ENSG00000114450"}},"GRch38":{"90":{"location":"3:179396089-179451590","ensembl_id":"ENSG00000114450"}}},"hgnc_date_symbol_changed":"2003-03-27"},"entity_type":"gene","entity_name":"GNB4","confidence_level":"1","penetrance":"Complete","mode_of_pathogenicity":"","publications":["28642160","27908631","23434117"],"evidence":["South West GLH","NHS GMS","London North GLH","Expert Review Red","Radboud University Medical Center, Nijmegen"],"phenotypes":["Charcot Marie Tooth disease, dominant intermediate F, 615185","Charcot Marie Tooth disease, dominant intermediate F, 615185"],"mode_of_inheritance":"MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted","tags":[],"panel":{"id":85,"hash_id":"55ad205422c1fc7041340234","name":"Hereditary neuropathy","disease_group":"Neurology and neurodevelopmental disorders","disease_sub_group":"Motor and Sensory Disorders of the PNS","status":"public","version":"1.333","version_created":"2019-07-09T13:10:50.031506Z","relevant_disorders":["Charcot-Marie-Tooth disease"],"stats":{"number_of_genes":276,"number_of_strs":11,"number_of_regions":2},"types":[{"name":"Rare Disease 100K","slug":"rare-disease-100k","description":"Rare Disease 100K"},{"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."}]}}]}