{"count":1,"next":null,"previous":null,"results":[{"gene_data":{"alias":["TR","CF2R","PAR1","PAR-1"],"biotype":"protein_coding","hgnc_id":"HGNC:3537","gene_name":"coagulation factor II thrombin receptor","omim_gene":["187930"],"alias_name":["protease activated receptor 1"],"gene_symbol":"F2R","hgnc_symbol":"F2R","hgnc_release":"2017-11-03","ensembl_genes":{"GRch37":{"82":{"location":"5:76011868-76031606","ensembl_id":"ENSG00000181104"}},"GRch38":{"90":{"location":"5:76716043-76735781","ensembl_id":"ENSG00000181104"}}},"hgnc_date_symbol_changed":"1991-07-16"},"entity_type":"gene","entity_name":"F2R","confidence_level":"2","penetrance":null,"mode_of_pathogenicity":"","publications":["26630678"],"evidence":["Expert Review Amber","North West GLH","Yorkshire and North East GLH","London South GLH","NHS GMS","Wessex and West Midlands GLH"],"phenotypes":["Type 1 VWD"],"mode_of_inheritance":"BOTH monoallelic and biallelic, autosomal or pseudoautosomal","tags":[],"panel":{"id":545,"hash_id":null,"name":"Bleeding and platelet disorders","disease_group":"","disease_sub_group":"","status":"public","version":"0.78","version_created":"2019-09-23T11:07:54.788299Z","relevant_disorders":["R90"],"stats":{"number_of_genes":111,"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)"}]}}]}