{"count":1,"next":null,"previous":null,"results":[{"gene_data":{"alias":[],"biotype":"protein_coding","hgnc_id":"HGNC:21011","gene_name":"carboxypeptidase O","omim_gene":["609563"],"alias_name":["metallocarboxypeptidase O","metallocarboxypeptidase C"],"gene_symbol":"CPO","hgnc_symbol":"CPO","hgnc_release":"2017-11-03","ensembl_genes":{"GRch37":{"82":{"location":"2:207804278-207834198","ensembl_id":"ENSG00000144410"}},"GRch38":{"90":{"location":"2:206939554-206969474","ensembl_id":"ENSG00000144410"}}},"hgnc_date_symbol_changed":"2004-01-29"},"entity_type":"gene","entity_name":"CPO","confidence_level":"2","penetrance":null,"mode_of_pathogenicity":"","publications":[],"evidence":["Expert Review Amber"],"phenotypes":[],"mode_of_inheritance":"","tags":[],"panel":{"id":563,"hash_id":null,"name":"Vascular skin disorders","disease_group":"","disease_sub_group":"","status":"public","version":"0.13","version_created":"2019-09-09T15:38:44.120161Z","relevant_disorders":[],"stats":{"number_of_genes":34,"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":"Component Of Super Panel","slug":"component-of-super-panel","description":"This panel is a component of a Super Panel"}]}}]}