{"count":1,"next":null,"previous":null,"results":[{"gene_data":{"alias":[],"biotype":"protein_coding","hgnc_id":"HGNC:11944","gene_name":"troponin C2, fast skeletal type","omim_gene":["191039"],"alias_name":null,"gene_symbol":"TNNC2","hgnc_symbol":"TNNC2","hgnc_release":"2017-11-03","ensembl_genes":{"GRch37":{"82":{"location":"20:44451853-44462384","ensembl_id":"ENSG00000101470"}},"GRch38":{"90":{"location":"20:45823214-45833745","ensembl_id":"ENSG00000101470"}}},"hgnc_date_symbol_changed":"1995-05-25"},"entity_type":"gene","entity_name":"TNNC2","confidence_level":"1","penetrance":null,"mode_of_pathogenicity":"","publications":["26924529"],"evidence":["NHS GMS","London South GLH"],"phenotypes":["congenital myopathy"],"mode_of_inheritance":"MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown","tags":[],"panel":{"id":225,"hash_id":"553f94b6bb5a1616e5ed459a","name":"Congenital myopathy","disease_group":"Neurology and neurodevelopmental disorders","disease_sub_group":"Neuromuscular disorders","status":"public","version":"1.166","version_created":"2019-10-09T12:41:32.789611Z","relevant_disorders":["R81"],"stats":{"number_of_genes":100,"number_of_strs":2,"number_of_regions":3},"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)"}]}}]}