{"count":1,"next":null,"previous":null,"results":[{"gene_data":{"alias":["RME8","KIAA0678"],"biotype":"protein_coding","hgnc_id":"HGNC:30343","gene_name":"DnaJ heat shock protein family (Hsp40) member C13","omim_gene":["614334"],"alias_name":null,"gene_symbol":"DNAJC13","hgnc_symbol":"DNAJC13","hgnc_release":"2017-11-03","ensembl_genes":{"GRch37":{"82":{"location":"3:132136370-132257876","ensembl_id":"ENSG00000138246"}},"GRch38":{"90":{"location":"3:132417526-132539032","ensembl_id":"ENSG00000138246"}}},"hgnc_date_symbol_changed":"2004-03-17"},"entity_type":"gene","entity_name":"DNAJC13","confidence_level":"2","penetrance":null,"mode_of_pathogenicity":"","publications":["24218364","25186792","30537300"],"evidence":["NHS GMS","Yorkshire and North East GLH","Expert Review Amber"],"phenotypes":[],"mode_of_inheritance":"MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown","tags":[],"panel":{"id":474,"hash_id":null,"name":"Neurodegenerative disorders - adult onset","disease_group":"","disease_sub_group":"","status":"public","version":"1.106","version_created":"2019-09-20T16:19:10.101841Z","relevant_disorders":["R58"],"stats":{"number_of_genes":395,"number_of_strs":18,"number_of_regions":4},"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."}]}}]}