{"count":1,"next":null,"previous":null,"results":[{"gene_data":{"alias":["MRG1"],"biotype":"protein_coding","hgnc_id":"HGNC:1987","gene_name":"Cbp/p300 interacting transactivator with Glu/Asp rich carboxy-terminal domain 2","omim_gene":["602937"],"alias_name":null,"gene_symbol":"CITED2","hgnc_symbol":"CITED2","hgnc_release":"2017-11-03T00:00:00","ensembl_genes":{"GRch37":{"82":{"location":"6:139693393-139695757","ensembl_id":"ENSG00000164442"}},"GRch38":{"90":{"location":"6:139371807-139374620","ensembl_id":"ENSG00000164442"}}},"hgnc_date_symbol_changed":"1999-06-11"},"entity_type":"gene","entity_name":"CITED2","confidence_level":"1","penetrance":"Complete","mode_of_pathogenicity":"","publications":["24848765, 16287139"],"evidence":["Expert Review Red","Radboud University Medical Center, Nijmegen","Literature"],"phenotypes":["Atrial septal defect, 8  614433,   Ventricular septal defect 2,  614431"],"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"}]}}]}