{"count":1,"next":null,"previous":null,"results":[{"gene_data":{"alias":["FLJ20142","dJ776P7.1","MACROD3"],"biotype":"protein_coding","hgnc_id":"HGNC:18010","gene_name":"ganglioside induced differentiation associated protein 2","omim_gene":null,"alias_name":null,"gene_symbol":"GDAP2","hgnc_symbol":"GDAP2","hgnc_release":"2017-11-03","ensembl_genes":{"GRch37":{"82":{"location":"1:118406107-118472253","ensembl_id":"ENSG00000196505"}},"GRch38":{"90":{"location":"1:117863485-117929630","ensembl_id":"ENSG00000196505"}}},"hgnc_date_symbol_changed":"2002-01-16"},"entity_type":"gene","entity_name":"GDAP2","confidence_level":"2","penetrance":null,"mode_of_pathogenicity":"","publications":[],"evidence":["Expert Review Amber","London North GLH","NHS GMS","Wessex and West Midlands GLH"],"phenotypes":["Autosomal recessive spinocerebellar ataxia"],"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."}]}}]}