{"count":1,"next":null,"previous":null,"results":[{"gene_data":{"alias":["H326","FLJ35857"],"biotype":"protein_coding","hgnc_id":"HGNC:24891","gene_name":"DDB1 and CUL4 associated factor 8","omim_gene":["615820"],"alias_name":null,"gene_symbol":"DCAF8","hgnc_symbol":"DCAF8","hgnc_release":"2017-11-03T00:00:00","ensembl_genes":{"GRch37":{"82":{"location":"1:160185505-160254920","ensembl_id":"ENSG00000132716"}},"GRch38":{"90":{"location":"1:160215715-160262531","ensembl_id":"ENSG00000132716"}}},"hgnc_date_symbol_changed":"2009-07-17"},"entity_type":"gene","entity_name":"DCAF8","confidence_level":"1","penetrance":"Complete","mode_of_pathogenicity":"","publications":["24500646"],"evidence":["NHS GMS","South West GLH","Expert Review Red","Expert Review"],"phenotypes":["?Giant axonal neuropathy 2, autosomal dominant, 610100"],"mode_of_inheritance":"MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted","tags":[],"panel":{"id":85,"hash_id":"55ad205422c1fc7041340234","name":"Hereditary neuropathy","disease_group":"Neurology and neurodevelopmental disorders","disease_sub_group":"Motor and Sensory Disorders of the PNS","status":"public","version":"1.333","version_created":"2019-07-09T13:10:50.031506Z","relevant_disorders":["Charcot-Marie-Tooth disease"],"stats":{"number_of_genes":276,"number_of_strs":11,"number_of_regions":2},"types":[{"name":"Rare Disease 100K","slug":"rare-disease-100k","description":"Rare Disease 100K"},{"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."}]}}]}