{"count":1,"next":null,"previous":null,"results":[{"gene_data":{"alias":["PKACg"],"biotype":"protein_coding","hgnc_id":"HGNC:9382","gene_name":"protein kinase cAMP-activated catalytic subunit gamma","omim_gene":["176893"],"alias_name":null,"gene_symbol":"PRKACG","hgnc_symbol":"PRKACG","hgnc_release":"2017-11-03","ensembl_genes":{"GRch37":{"82":{"location":"9:71627469-71629039","ensembl_id":"ENSG00000165059"}},"GRch38":{"90":{"location":"9:69012529-69014113","ensembl_id":"ENSG00000165059"}}},"hgnc_date_symbol_changed":"2001-06-22"},"entity_type":"gene","entity_name":"PRKACG","confidence_level":"3","penetrance":null,"mode_of_pathogenicity":"","publications":["25061177"],"evidence":["North West GLH","Yorkshire and North East GLH","London South GLH","NHS GMS","Expert Review Green","Wessex and West Midlands GLH"],"phenotypes":["616176BLEEDING DISORDER, PLATELET-TYPE, 19","616176 BLEEDING DISORDER, PLATELET-TYPE, 19","BDPLT19"],"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)"}]}}]}