{"count":1,"next":null,"previous":null,"results":[{"gene_data":{"alias":["Pet-1"],"biotype":"protein_coding","hgnc_id":"HGNC:18562","gene_name":"FEV, ETS transcription factor","omim_gene":["607150"],"alias_name":null,"gene_symbol":"FEV","hgnc_symbol":"FEV","hgnc_release":"2017-11-03T00:00:00","ensembl_genes":{"GRch37":{"82":{"location":"2:219845809-219850379","ensembl_id":"ENSG00000163497"}},"GRch38":{"90":{"location":"2:218981087-218985657","ensembl_id":"ENSG00000163497"}}},"hgnc_date_symbol_changed":"2004-03-19"},"entity_type":"gene","entity_name":"FEV","confidence_level":"0","penetrance":"Complete","mode_of_pathogenicity":"","publications":[],"evidence":["Expert Review Removed","Literature"],"phenotypes":["SIDS","Sudden infant death syndrome"],"mode_of_inheritance":"MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown","tags":[],"panel":{"id":45,"hash_id":"5763f6508f620350a1996055","name":"Sudden death in young people","disease_group":"Cardiovascular disorders","disease_sub_group":"Cardiac arrhythmia","status":"public","version":"1.12","version_created":"2019-06-20T15:15:17.414434Z","relevant_disorders":["Unexplained sudden death in the young"],"stats":{"number_of_genes":35,"number_of_strs":0,"number_of_regions":0},"types":[{"name":"Rare Disease 100K","slug":"rare-disease-100k","description":"Rare Disease 100K"}]}}]}