{"count":1,"next":null,"previous":null,"results":[{"gene_data":{"alias":["T54","GPATC5","GPATCH5","Spp2"],"biotype":"protein_coding","hgnc_id":"HGNC:30677","gene_name":"G-patch domain and KOW motifs","omim_gene":["301003"],"alias_name":["G patch domain containing 5"],"gene_symbol":"GPKOW","hgnc_symbol":"GPKOW","hgnc_release":"2017-11-03","ensembl_genes":{"GRch37":{"82":{"location":"X:48970334-48980151","ensembl_id":"ENSG00000068394"}},"GRch38":{"90":{"location":"X:49113389-49123801","ensembl_id":"ENSG00000068394"}}},"hgnc_date_symbol_changed":"2004-05-11"},"entity_type":"gene","entity_name":"GPKOW","confidence_level":"2","penetrance":null,"mode_of_pathogenicity":"","publications":["28612833"],"evidence":["Expert Review Amber","PAGE Additional Gene List"],"phenotypes":["male-lethal microcephaly with intrauterine growth restriction"],"mode_of_inheritance":"X-LINKED: hemizygous mutation in males, biallelic mutations in females","tags":[],"panel":{"id":478,"hash_id":null,"name":"Fetal anomalies","disease_group":"","disease_sub_group":"","status":"public","version":"0.344","version_created":"2019-09-17T09:38:10.568007Z","relevant_disorders":["R21"],"stats":{"number_of_genes":1721,"number_of_strs":0,"number_of_regions":0},"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."}]}}]}