{"count":1,"next":null,"previous":null,"results":[{"gene_data":{"alias":["ZNF912"],"biotype":"protein_coding","hgnc_id":"HGNC:9045","gene_name":"PLAG1 zinc finger","omim_gene":["603026"],"alias_name":null,"gene_symbol":"PLAG1","hgnc_symbol":"PLAG1","hgnc_release":"2017-11-03","ensembl_genes":{"GRch37":{"82":{"location":"8:57073463-57123883","ensembl_id":"ENSG00000181690"}},"GRch38":{"90":{"location":"8:56160904-56211324","ensembl_id":"ENSG00000181690"}}},"hgnc_date_symbol_changed":"1998-02-11"},"entity_type":"gene","entity_name":"PLAG1","confidence_level":"3","penetrance":null,"mode_of_pathogenicity":"","publications":["28796236"],"evidence":["Expert Review Green","Expert list"],"phenotypes":["SRS","Silver-Russell syndrome"],"mode_of_inheritance":"MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted","tags":[],"panel":{"id":473,"hash_id":null,"name":"Growth failure in early childhood","disease_group":"","disease_sub_group":"","status":"public","version":"1.3","version_created":"2019-08-14T09:11:49.488162Z","relevant_disorders":["R147"],"stats":{"number_of_genes":126,"number_of_strs":0,"number_of_regions":5},"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."},{"name":"GMS signed-off","slug":"gms-signed-off","description":"This panel has undergone review by a NHSE GMS disease specialist group and processes to be signed-off for use within the GMS."}]}}]}