{"count":1,"next":null,"previous":null,"results":[{"gene_data":{"alias":[],"biotype":"protein_coding","hgnc_id":"HGNC:2637","gene_name":"cytochrome P450 family 3 subfamily A member 4","omim_gene":["124010"],"alias_name":null,"gene_symbol":"CYP3A4","hgnc_symbol":"CYP3A4","hgnc_release":"2017-11-03","ensembl_genes":{"GRch37":{"82":{"location":"7:99354604-99381888","ensembl_id":"ENSG00000160868"}},"GRch38":{"90":{"location":"7:99756960-99784265","ensembl_id":"ENSG00000160868"}}},"hgnc_date_symbol_changed":"1990-02-24"},"entity_type":"gene","entity_name":"CYP3A4","confidence_level":"2","penetrance":null,"mode_of_pathogenicity":"","publications":["29461981"],"evidence":["Expert Review Amber","NHS GMS"],"phenotypes":[],"mode_of_inheritance":"MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted","tags":[],"panel":{"id":482,"hash_id":null,"name":"Hypophosphataemia or rickets","disease_group":"","disease_sub_group":"","status":"public","version":"2.1","version_created":"2019-07-31T12:01:20.025463Z","relevant_disorders":["R154"],"stats":{"number_of_genes":14,"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."},{"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."}]}}]}