{"count":2,"next":null,"previous":null,"results":[{"gene_data":{"alias":[],"biotype":"protein_coding","hgnc_id":"HGNC:11843","gene_name":"tolloid like 1","omim_gene":["606742"],"alias_name":null,"gene_symbol":"TLL1","hgnc_symbol":"TLL1","hgnc_release":"2017-11-03T00:00:00","ensembl_genes":{"GRch37":{"82":{"location":"4:166794410-167025047","ensembl_id":"ENSG00000038295"}},"GRch38":{"90":{"location":"4:165873258-166103895","ensembl_id":"ENSG00000038295"}}},"hgnc_date_symbol_changed":"1997-10-16"},"entity_type":"gene","entity_name":"TLL1","confidence_level":"1","penetrance":"Complete","mode_of_pathogenicity":"","publications":["18830233"],"evidence":["Expert Review Red","Radboud University Medical Center, Nijmegen","Literature"],"phenotypes":["Atrial septal defect 6  613087"],"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":[],"biotype":"protein_coding","hgnc_id":"HGNC:11843","gene_name":"tolloid like 1","omim_gene":["606742"],"alias_name":null,"gene_symbol":"TLL1","hgnc_symbol":"TLL1","hgnc_release":"2017-11-03","ensembl_genes":{"GRch37":{"82":{"location":"4:166794410-167025047","ensembl_id":"ENSG00000038295"}},"GRch38":{"90":{"location":"4:165873258-166103895","ensembl_id":"ENSG00000038295"}}},"hgnc_date_symbol_changed":"1997-10-16"},"entity_type":"gene","entity_name":"TLL1","confidence_level":"1","penetrance":null,"mode_of_pathogenicity":"Other - please provide details in the comments","publications":["18830233"],"evidence":["DD-Gene2Phenotype","Expert Review Red"],"phenotypes":["ATRIAL SEPTAL DEFECT TYPE 6 613087"],"mode_of_inheritance":"MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown","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"}]}}]}