{"count":1,"next":null,"previous":null,"results":[{"gene_data":{"alias":["COX1","PGHS-1","PTGHS"],"biotype":"protein_coding","hgnc_id":"HGNC:9604","gene_name":"prostaglandin-endoperoxide synthase 1","omim_gene":["176805"],"alias_name":["cyclooxygenase-1"],"gene_symbol":"PTGS1","hgnc_symbol":"PTGS1","hgnc_release":"2017-11-03","ensembl_genes":{"GRch37":{"82":{"location":"9:125132824-125157982","ensembl_id":"ENSG00000095303"}},"GRch38":{"90":{"location":"9:122370530-122395703","ensembl_id":"ENSG00000095303"}}},"hgnc_date_symbol_changed":"1992-10-27"},"entity_type":"gene","entity_name":"PTGS1","confidence_level":"2","penetrance":null,"mode_of_pathogenicity":"","publications":["11442478","27629384","8562397","28748566","6103258"],"evidence":["Expert Review Amber","North West GLH","Yorkshire and North East GLH","London South GLH","NHS GMS","Wessex and West Midlands GLH"],"phenotypes":["BDPLT12","605735 BLEEDING DISORDER, PLATELET-TYPE, 12"],"mode_of_inheritance":"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)"}]}}]}