{"count":1,"next":null,"previous":null,"results":[{"gene_data":{"alias":["ICF45","FLJ11601","FLJ20546","IHG-1","hTHG1"],"biotype":"protein_coding","hgnc_id":"HGNC:26053","gene_name":"tRNA-histidine guanylyltransferase 1 like","omim_gene":null,"alias_name":["interphase cytoplasmic foci protein 45","induced by high glucose-1"],"gene_symbol":"THG1L","hgnc_symbol":"THG1L","hgnc_release":"2017-11-03","ensembl_genes":{"GRch37":{"82":{"location":"5:157158205-157168456","ensembl_id":"ENSG00000113272"}},"GRch38":{"90":{"location":"5:157731197-157741448","ensembl_id":"ENSG00000113272"}}},"hgnc_date_symbol_changed":"2006-09-01"},"entity_type":"gene","entity_name":"THG1L","confidence_level":"1","penetrance":null,"mode_of_pathogenicity":"","publications":[],"evidence":["NHS GMS","Wessex and West Midlands GLH"],"phenotypes":["Cerebellar ataxia with developmental delay"],"mode_of_inheritance":"BIALLELIC, autosomal or pseudoautosomal","tags":[],"panel":{"id":466,"hash_id":null,"name":"Hereditary ataxia - adult onset","disease_group":"","disease_sub_group":"","status":"public","version":"1.211","version_created":"2019-09-20T14:18:40.957460Z","relevant_disorders":["Hereditary ataxia with onset in adulthood","R54"],"stats":{"number_of_genes":236,"number_of_strs":13,"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."}]}}]}