{"count":1,"next":null,"previous":null,"results":[{"gene_data":{"alias":["RGNEF","p190RhoGEF","RIP2"],"biotype":"protein_coding","hgnc_id":"HGNC:30322","gene_name":"Rho guanine nucleotide exchange factor 28","omim_gene":["612790"],"alias_name":null,"gene_symbol":"ARHGEF28","hgnc_symbol":"ARHGEF28","hgnc_release":"2017-11-03","ensembl_genes":{"GRch37":{"82":{"location":"5:72921983-73237818","ensembl_id":"ENSG00000214944"}},"GRch38":{"90":{"location":"5:73626158-73941993","ensembl_id":"ENSG00000214944"}}},"hgnc_date_symbol_changed":"2012-08-08"},"entity_type":"gene","entity_name":"ARHGEF28","confidence_level":"2","penetrance":null,"mode_of_pathogenicity":"","publications":["23286752","24712971","28709720","27154192"],"evidence":["NHS GMS","Yorkshire and North East GLH","Expert Review Amber"],"phenotypes":["Amyotrophic lateral sclerosis"],"mode_of_inheritance":"BOTH monoallelic and biallelic, autosomal or pseudoautosomal","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."}]}}]}