{"count":1,"next":null,"previous":null,"results":[{"gene_data":{"alias":["NF-ATC","NFATc","NFAT2"],"biotype":"protein_coding","hgnc_id":"HGNC:7775","gene_name":"nuclear factor of activated T-cells 1","omim_gene":["600489"],"alias_name":null,"gene_symbol":"NFATC1","hgnc_symbol":"NFATC1","hgnc_release":"2017-11-03T00:00:00","ensembl_genes":{"GRch37":{"82":{"location":"18:77155856-77289325","ensembl_id":"ENSG00000131196"}},"GRch38":{"90":{"location":"18:79395856-79529325","ensembl_id":"ENSG00000131196"}}},"hgnc_date_symbol_changed":"1994-11-16"},"entity_type":"gene","entity_name":"NFATC1","confidence_level":"1","penetrance":"Complete","mode_of_pathogenicity":"","publications":["http://dx.doi.org/10.1371/journal.pgen.1002843"],"evidence":["Expert Review Red","Radboud University Medical Center, Nijmegen"],"phenotypes":["Tetralogy of Fallot (Silversides (2012) PLoS Genet 8)"],"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"}]}}]}