{"count":1,"next":null,"previous":null,"results":[{"gene_data":{"alias":["KIAA0517","RNF86","CMT2R"],"biotype":"protein_coding","hgnc_id":"HGNC:15974","gene_name":"tripartite motif containing 2","omim_gene":["614141"],"alias_name":null,"gene_symbol":"TRIM2","hgnc_symbol":"TRIM2","hgnc_release":"2017-11-03T00:00:00","ensembl_genes":{"GRch37":{"82":{"location":"4:154073494-154260472","ensembl_id":"ENSG00000109654"}},"GRch38":{"90":{"location":"4:153152342-153339320","ensembl_id":"ENSG00000109654"}}},"hgnc_date_symbol_changed":"2001-07-18"},"entity_type":"gene","entity_name":"TRIM2","confidence_level":"1","penetrance":"Complete","mode_of_pathogenicity":"","publications":["23562820","25893792","18687884"],"evidence":["South West GLH","NHS GMS","London North GLH","Expert Review Red","Expert Review"],"phenotypes":["Charcot-Marie-Tooth disease, type 2R, 615490"],"mode_of_inheritance":"BIALLELIC, autosomal or pseudoautosomal","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."}]}}]}