{"count":1,"next":null,"previous":null,"results":[{"gene_data":{"alias":[],"biotype":"protein_coding","hgnc_id":"HGNC:6129","gene_name":"iroquois homeobox 4","omim_gene":["606199"],"alias_name":null,"gene_symbol":"IRX4","hgnc_symbol":"IRX4","hgnc_release":"2017-11-03T00:00:00","ensembl_genes":{"GRch37":{"82":{"location":"5:1877541-1887350","ensembl_id":"ENSG00000113430"}},"GRch38":{"90":{"location":"5:1877413-1887236","ensembl_id":"ENSG00000113430"}}},"hgnc_date_symbol_changed":"2000-06-09"},"entity_type":"gene","entity_name":"IRX4","confidence_level":"1","penetrance":"Complete","mode_of_pathogenicity":"","publications":["21544582"],"evidence":["Expert Review Red","Literature"],"phenotypes":["Ventricular septal defect"],"mode_of_inheritance":"MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted","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"}]}}]}