{"count":1,"next":null,"previous":null,"results":[{"gene_data":{"alias":["FREAC7","FKH6"],"biotype":"protein_coding","hgnc_id":"HGNC:3817","gene_name":"forkhead box L1","omim_gene":["603252"],"alias_name":null,"gene_symbol":"FOXL1","hgnc_symbol":"FOXL1","hgnc_release":"2017-11-03T00:00:00","ensembl_genes":{"GRch37":{"82":{"location":"16:86609974-86615303","ensembl_id":"ENSG00000176678"}},"GRch38":{"90":{"location":"16:86576368-86582160","ensembl_id":"ENSG00000176678"}}},"hgnc_date_symbol_changed":"1995-06-05"},"entity_type":"gene","entity_name":"FOXL1","confidence_level":"1","penetrance":"Complete","mode_of_pathogenicity":"","publications":["DOI: 10.1111/j.1399-0004.2011.01674.x"],"evidence":["Expert Review Red","Radboud University Medical Center, Nijmegen"],"phenotypes":["Hypoplastic left heart syndrome (Iascone (2012) Clin Genet 81,542)"],"mode_of_inheritance":"","tags":[],"panel":{"id":212,"hash_id":"583c128f8f62036f70db8d29","name":"Familial non syndromic congenital heart disease","disease_group":"Cardiovascular disorders","disease_sub_group":"Congenital heart disease","status":"public","version":"1.49","version_created":"2019-08-07T15:17:24.060112Z","relevant_disorders":["Fallots tetralogy","Hypoplastic Left Heart Syndrome","Left Ventricular Outflow Tract obstruction disorders","Pulmonary atresia","Transposition of the great vessels","Familial non-syndromic congenital heart disease","Familial congenital heart disease","Congenital heart disease","Syndromic congenital heart disease","Isomerism and laterality disorders"],"stats":{"number_of_genes":47,"number_of_strs":0,"number_of_regions":8},"types":[{"name":"Rare Disease 100K","slug":"rare-disease-100k","description":"Rare Disease 100K"}]}}]}