{"count":2,"next":null,"previous":null,"results":[{"gene_data":{"alias":["KIAA0620"],"biotype":"protein_coding","hgnc_id":"HGNC:9107","gene_name":"plexin D1","omim_gene":["604282"],"alias_name":null,"gene_symbol":"PLXND1","hgnc_symbol":"PLXND1","hgnc_release":"2017-11-03T00:00:00","ensembl_genes":{"GRch37":{"82":{"location":"3:129274018-129325661","ensembl_id":"ENSG00000004399"}},"GRch38":{"90":{"location":"3:129555175-129606818","ensembl_id":"ENSG00000004399"}}},"hgnc_date_symbol_changed":"1999-11-19"},"entity_type":"gene","entity_name":"PLXND1","confidence_level":"1","penetrance":"Complete","mode_of_pathogenicity":"","publications":["25713110"],"evidence":["Expert Review Red","Literature"],"phenotypes":["Truncus arteriosus"],"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"}]}},{"gene_data":{"alias":["KIAA0620"],"biotype":"protein_coding","hgnc_id":"HGNC:9107","gene_name":"plexin D1","omim_gene":["604282"],"alias_name":null,"gene_symbol":"PLXND1","hgnc_symbol":"PLXND1","hgnc_release":"2017-11-03","ensembl_genes":{"GRch37":{"82":{"location":"3:129274018-129325661","ensembl_id":"ENSG00000004399"}},"GRch38":{"90":{"location":"3:129555175-129606818","ensembl_id":"ENSG00000004399"}}},"hgnc_date_symbol_changed":"1999-11-19"},"entity_type":"gene","entity_name":"PLXND1","confidence_level":"1","penetrance":null,"mode_of_pathogenicity":"Other - please provide details in the comments","publications":["24254849"],"evidence":["DD-Gene2Phenotype","Expert Review Red"],"phenotypes":["MOEBIUS SYNDROME","TRUNCUS ARTERIOSIS"],"mode_of_inheritance":"BOTH monoallelic and biallelic, autosomal or pseudoautosomal","tags":[],"panel":{"id":484,"hash_id":null,"name":"DDG2P","disease_group":"","disease_sub_group":"","status":"public","version":"1.137","version_created":"2019-10-08T15:56:59.220133Z","relevant_disorders":[],"stats":{"number_of_genes":1893,"number_of_strs":0,"number_of_regions":0},"types":[{"name":"GMS Rare Disease","slug":"gms-rare-disease","description":"This panel type is used for GMS panels that are not virtual (i.e. could be a wet lab test)"},{"name":"Component Of Super Panel","slug":"component-of-super-panel","description":"This panel is a component of a Super Panel"}]}}]}