{"count":1,"next":null,"previous":null,"results":[{"gene_data":{"alias":[],"biotype":"protein_coding","hgnc_id":"HGNC:7613","gene_name":"myomesin 1","omim_gene":["603508"],"alias_name":["skelemin"],"gene_symbol":"MYOM1","hgnc_symbol":"MYOM1","hgnc_release":"2017-11-03T00:00:00","ensembl_genes":{"GRch37":{"82":{"location":"18:3066805-3220106","ensembl_id":"ENSG00000101605"}},"GRch38":{"90":{"location":"18:3066807-3220108","ensembl_id":"ENSG00000101605"}}},"hgnc_date_symbol_changed":"1998-12-09"},"entity_type":"gene","entity_name":"MYOM1","confidence_level":"1","penetrance":"Complete","mode_of_pathogenicity":"","publications":[],"evidence":["South West GLH","Expert list"],"phenotypes":[],"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)"}]}}]}