{"count":1,"next":null,"previous":null,"results":[{"gene_data":{"alias":["SDR9C3"],"biotype":"protein_coding","hgnc_id":"HGNC:5209","gene_name":"hydroxysteroid 11-beta dehydrogenase 2","omim_gene":["614232"],"alias_name":["short chain dehydrogenase/reductase family 9C, member 3"],"gene_symbol":"HSD11B2","hgnc_symbol":"HSD11B2","hgnc_release":"2017-11-03T00:00:00","ensembl_genes":{"GRch37":{"82":{"location":"16:67464555-67471456","ensembl_id":"ENSG00000176387"}},"GRch38":{"90":{"location":"16:67430652-67437553","ensembl_id":"ENSG00000176387"}}},"hgnc_date_symbol_changed":"1994-11-18"},"entity_type":"gene","entity_name":"HSD11B2","confidence_level":"3","penetrance":"Complete","mode_of_pathogenicity":"","publications":["17314322","15126515","12788846"],"evidence":["Expert Review Green","Literature","Radboud University Medical Center, Nijmegen","UKGTN","Expert"],"phenotypes":["Apparent mineralocorticoid excess,\t218030"],"mode_of_inheritance":"BIALLELIC, autosomal or pseudoautosomal","tags":[],"panel":{"id":314,"hash_id":"553f9697bb5a1616e5ed45d4","name":"Extreme early-onset hypertension","disease_group":"Renal and urinary tract disorders","disease_sub_group":"Disorders of function","status":"public","version":"1.10","version_created":"2018-12-16T17:33:34.572280Z","relevant_disorders":[],"stats":{"number_of_genes":25,"number_of_strs":0,"number_of_regions":0},"types":[{"name":"Rare Disease 100K","slug":"rare-disease-100k","description":"Rare Disease 100K"},{"name":"GMS Rare Disease Virtual","slug":"gms-rare-disease-virtual","description":"This is a panel for the Genomic Medicine Service for an exome/genome/panel based test that requires a virtual gene panel for rare disease in the Test Directory."}]}}]}