{"count":1,"next":null,"previous":null,"results":[{"gene_data":{"alias":["MURF-1","IRF","SMRZ"],"biotype":"protein_coding","hgnc_id":"HGNC:16007","gene_name":"tripartite motif containing 63","omim_gene":["606131"],"alias_name":["muscle-specific RING finger protein 1","iris ring finger protein","striated muscle RING zinc finger protein"],"gene_symbol":"TRIM63","hgnc_symbol":"TRIM63","hgnc_release":"2017-11-03T00:00:00","ensembl_genes":{"GRch37":{"82":{"location":"1:26377795-26394927","ensembl_id":"ENSG00000158022"}},"GRch38":{"90":{"location":"1:26051304-26068436","ensembl_id":"ENSG00000158022"}}},"hgnc_date_symbol_changed":"2004-11-17"},"entity_type":"gene","entity_name":"TRIM63","confidence_level":"1","penetrance":"Complete","mode_of_pathogenicity":"","publications":[],"evidence":["South West GLH","Literature"],"phenotypes":["Hypertrophic cardiomyopathy"],"mode_of_inheritance":"Unknown","tags":[],"panel":{"id":49,"hash_id":"55a39e2d22c1fc6711b0c6b3","name":"Hypertrophic cardiomyopathy - teen and adult","disease_group":"Cardiovascular disorders","disease_sub_group":"Cardiomyopathy","status":"public","version":"1.77","version_created":"2019-10-02T12:51:19.933333Z","relevant_disorders":["Hypertrophic Cardiomyopathy","HCM","R131"],"stats":{"number_of_genes":70,"number_of_strs":1,"number_of_regions":0},"types":[{"name":"Rare Disease 100K","slug":"rare-disease-100k","description":"Rare Disease 100K"},{"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)"}]}}]}