{"count":2,"next":null,"previous":null,"results":[{"gene_data":{"alias":[],"biotype":"protein_coding","hgnc_id":"HGNC:7939","gene_name":"natriuretic peptide A","omim_gene":["108780"],"alias_name":null,"gene_symbol":"NPPA","hgnc_symbol":"NPPA","hgnc_release":"2017-11-03T00:00:00","ensembl_genes":{"GRch37":{"82":{"location":"1:11905766-11908402","ensembl_id":"ENSG00000175206"}},"GRch38":{"90":{"location":"1:11845709-11848345","ensembl_id":"ENSG00000175206"}}},"hgnc_date_symbol_changed":"1986-01-01"},"entity_type":"gene","entity_name":"NPPA","confidence_level":"1","penetrance":"Complete","mode_of_pathogenicity":"","publications":["23275345","doi:10.​1007/​s12265-016-9673-5"],"evidence":["South West GLH","Literature"],"phenotypes":["Dilated cardiomyopathy"],"mode_of_inheritance":"BOTH monoallelic and biallelic, autosomal or pseudoautosomal","tags":[],"panel":{"id":47,"hash_id":"55a4d99022c1fc6710839b84","name":"Dilated Cardiomyopathy and conduction defects","disease_group":"Cardiovascular disorders","disease_sub_group":"Cardiomyopathy","status":"public","version":"1.63","version_created":"2019-09-30T12:02:00.646768Z","relevant_disorders":["Dilated Cardiomyopathy","Dilated Cardiomyopathy (DCM)","Dilated cardiomyopathy - teen and adult"],"stats":{"number_of_genes":84,"number_of_strs":0,"number_of_regions":0},"types":[{"name":"Rare Disease 100K","slug":"rare-disease-100k","description":"Rare Disease 100K"}]}},{"gene_data":{"alias":[],"biotype":"protein_coding","hgnc_id":"HGNC:7939","gene_name":"natriuretic peptide A","omim_gene":["108780"],"alias_name":null,"gene_symbol":"NPPA","hgnc_symbol":"NPPA","hgnc_release":"2017-11-03","ensembl_genes":{"GRch37":{"82":{"location":"1:11905766-11908402","ensembl_id":"ENSG00000175206"}},"GRch38":{"90":{"location":"1:11845709-11848345","ensembl_id":"ENSG00000175206"}}},"hgnc_date_symbol_changed":"1986-01-01"},"entity_type":"gene","entity_name":"NPPA","confidence_level":"1","penetrance":null,"mode_of_pathogenicity":"","publications":["26888179","23275345"],"evidence":["London South GLH","Expert Review Red","London South GLH","Expert Review Red"],"phenotypes":["Dilated cardiomyopathy"],"mode_of_inheritance":"Unknown","tags":[],"panel":{"id":750,"hash_id":null,"name":"Sudden cardiac death","disease_group":"","disease_sub_group":"","status":"public","version":"0.10","version_created":"2019-09-24T10:05:54.784946Z","relevant_disorders":["Molecular autopsy","R138"],"stats":{"number_of_genes":119,"number_of_strs":0,"number_of_regions":0},"types":[{"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":"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)"}]}}]}