{"count":1,"next":null,"previous":null,"results":[{"gene_data":{"alias":[],"biotype":"protein_coding","hgnc_id":"HGNC:5033","gene_name":"heterogeneous nuclear ribonucleoprotein A2/B1","omim_gene":["600124"],"alias_name":null,"gene_symbol":"HNRNPA2B1","hgnc_symbol":"HNRNPA2B1","hgnc_release":"2017-11-03","ensembl_genes":{"GRch37":{"82":{"location":"7:26229547-26241149","ensembl_id":"ENSG00000122566"}},"GRch38":{"90":{"location":"7:26189927-26201529","ensembl_id":"ENSG00000122566"}}},"hgnc_date_symbol_changed":"2007-08-16"},"entity_type":"gene","entity_name":"HNRNPA2B1","confidence_level":"2","penetrance":null,"mode_of_pathogenicity":"","publications":["25299611","23455423","27773581"],"evidence":["NHS GMS","Yorkshire and North East GLH","Expert Review Amber"],"phenotypes":["Amyotrophic lateral sclerosis"],"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."}]}}]}