{"count":1,"next":null,"previous":null,"results":[{"gene_data":{"alias":["CD142","TF"],"biotype":"protein_coding","hgnc_id":"HGNC:3541","gene_name":"coagulation factor III, tissue factor","omim_gene":["134390"],"alias_name":["tissue factor"],"gene_symbol":"F3","hgnc_symbol":"F3","hgnc_release":"2017-11-03","ensembl_genes":{"GRch37":{"82":{"location":"1:94994781-95007356","ensembl_id":"ENSG00000117525"}},"GRch38":{"90":{"location":"1:94529225-94541800","ensembl_id":"ENSG00000117525"}}},"hgnc_date_symbol_changed":"2001-06-22"},"entity_type":"gene","entity_name":"F3","confidence_level":"2","penetrance":null,"mode_of_pathogenicity":"","publications":[],"evidence":["Wessex and West Midlands GLH","Expert Review Amber","NHS GMS","London South GLH"],"phenotypes":["Tissue factor deficiency (Factor III)"],"mode_of_inheritance":"BOTH monoallelic and biallelic (but BIALLELIC mutations cause a more SEVERE disease form), autosomal or pseudoautosomal","tags":[],"panel":{"id":516,"hash_id":null,"name":"Thrombophilia","disease_group":"","disease_sub_group":"","status":"public","version":"1.0","version_created":"2019-09-23T14:53:24.252789Z","relevant_disorders":["R97"],"stats":{"number_of_genes":20,"number_of_strs":0,"number_of_regions":0},"types":[{"name":"GMS Rare Disease","slug":"gms-rare-disease","description":"This panel type is used for GMS panels that are not virtual (i.e. could be a wet lab test)"},{"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."}]}}]}