{"count":1,"next":null,"previous":null,"results":[{"gene_data":{"alias":["FBX1","FBXO1"],"biotype":"protein_coding","hgnc_id":"HGNC:1591","gene_name":"cyclin F","omim_gene":["600227"],"alias_name":null,"gene_symbol":"CCNF","hgnc_symbol":"CCNF","hgnc_release":"2017-11-03","ensembl_genes":{"GRch37":{"82":{"location":"16:2479395-2508855","ensembl_id":"ENSG00000162063"}},"GRch38":{"90":{"location":"16:2429394-2458854","ensembl_id":"ENSG00000162063"}}},"hgnc_date_symbol_changed":"1994-05-18"},"entity_type":"gene","entity_name":"CCNF","confidence_level":"3","penetrance":null,"mode_of_pathogenicity":"","publications":["27080313","29102476","30008669"],"evidence":["Yorkshire and North East GLH","Expert Review Green","NHS GMS","London North GLH"],"phenotypes":["Frontotemporal dementia / 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."}]}}]}