{"count":1,"next":null,"previous":null,"results":[{"gene_data":{"alias":[],"biotype":"protein_coding","hgnc_id":"HGNC:11640","gene_name":"transcription factor 7 like 1","omim_gene":["604652"],"alias_name":null,"gene_symbol":"TCF7L1","hgnc_symbol":"TCF7L1","hgnc_release":"2017-11-03","ensembl_genes":{"GRch37":{"82":{"location":"2:85360533-85537511","ensembl_id":"ENSG00000152284"}},"GRch38":{"90":{"location":"2:85133410-85310388","ensembl_id":"ENSG00000152284"}}},"hgnc_date_symbol_changed":"1998-01-20"},"entity_type":"gene","entity_name":"TCF7L1","confidence_level":"2","penetrance":null,"mode_of_pathogenicity":"","publications":["26764381"],"evidence":["Expert Review Amber","Literature"],"phenotypes":["No OMIM number","pituitary hormone deficiency"],"mode_of_inheritance":"MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown","tags":[],"panel":{"id":483,"hash_id":null,"name":"Pituitary hormone deficiency","disease_group":"","disease_sub_group":"","status":"public","version":"2.0","version_created":"2019-07-31T14:30:21.964840Z","relevant_disorders":["R159"],"stats":{"number_of_genes":50,"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."}]}}]}