{"count":2,"next":null,"previous":null,"results":[{"gene_data":{"alias":["CSX2","NKX4-2"],"biotype":"protein_coding","hgnc_id":"HGNC:32940","gene_name":"NK2 homeobox 6","omim_gene":["611770"],"alias_name":["tinman paralog (Drosophila)"],"gene_symbol":"NKX2-6","hgnc_symbol":"NKX2-6","hgnc_release":"2017-11-03T00:00:00","ensembl_genes":{"GRch37":{"82":{"location":"8:23559964-23564111","ensembl_id":"ENSG00000180053"}},"GRch38":{"90":{"location":"8:23702451-23706598","ensembl_id":"ENSG00000180053"}}},"hgnc_date_symbol_changed":"2006-06-29"},"entity_type":"gene","entity_name":"NKX2-6","confidence_level":"1","penetrance":"Complete","mode_of_pathogenicity":"","publications":["15649947, 24421281"],"evidence":["Expert Review Red","Radboud University Medical Center, Nijmegen","Literature"],"phenotypes":["Conotruncal heart malformations  217095, Persistent truncus arteriosus  217095"],"mode_of_inheritance":"BIALLELIC, autosomal or pseudoautosomal","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"}]}},{"gene_data":{"alias":["CSX2","NKX4-2"],"biotype":"protein_coding","hgnc_id":"HGNC:32940","gene_name":"NK2 homeobox 6","omim_gene":["611770"],"alias_name":["tinman paralog (Drosophila)"],"gene_symbol":"NKX2-6","hgnc_symbol":"NKX2-6","hgnc_release":"2017-11-03T00:00:00","ensembl_genes":{"GRch37":{"82":{"location":"8:23559964-23564111","ensembl_id":"ENSG00000180053"}},"GRch38":{"90":{"location":"8:23702451-23706598","ensembl_id":"ENSG00000180053"}}},"hgnc_date_symbol_changed":"2006-06-29"},"entity_type":"gene","entity_name":"NKX2-6","confidence_level":"1","penetrance":"Complete","mode_of_pathogenicity":"","publications":[],"evidence":["Expert Review Red"],"phenotypes":["CONOTRUNCAL HEART MALFORMATIONS","CTHM"],"mode_of_inheritance":"Unknown","tags":[],"panel":{"id":81,"hash_id":"57acb8268f620364dc61afd3","name":"Clefting","disease_group":"Dysmorphic and congenital abnormality syndromes","disease_sub_group":"Dysmorphic disorders","status":"public","version":"1.59","version_created":"2019-09-03T09:03:20.170928Z","relevant_disorders":["Familial non-syndromic cleft lip and or familial cleft palate","Familial non-syndromic clefting","Syndromic cleft lip and or cleft palate","Syndromic clefting"],"stats":{"number_of_genes":258,"number_of_strs":0,"number_of_regions":5},"types":[{"name":"Rare Disease 100K","slug":"rare-disease-100k","description":"Rare Disease 100K"},{"name":"GMS Rare Disease Virtual","slug":"gms-rare-disease-virtual","description":"This is a panel for the Genomic Medicine Service for an exome/genome/panel based test that requires a virtual gene panel for rare disease in the Test Directory."},{"name":"Component Of Super Panel","slug":"component-of-super-panel","description":"This panel is a component of a Super Panel"}]}}]}