{"count":1,"next":null,"previous":null,"results":[{"gene_data":{"alias":[],"biotype":"protein_coding","hgnc_id":"HGNC:3402","gene_name":"epoxide hydrolase 2","omim_gene":["132811"],"alias_name":null,"gene_symbol":"EPHX2","hgnc_symbol":"EPHX2","hgnc_release":"2017-11-03T00:00:00","ensembl_genes":{"GRch37":{"82":{"location":"8:27348296-27403081","ensembl_id":"ENSG00000120915"}},"GRch38":{"90":{"location":"8:27490779-27545564","ensembl_id":"ENSG00000120915"}}},"hgnc_date_symbol_changed":"1994-07-26"},"entity_type":"gene","entity_name":"EPHX2","confidence_level":"1","penetrance":"Complete","mode_of_pathogenicity":"","publications":[],"evidence":["Radboud University Medical Center, Nijmegen"],"phenotypes":["Hypercholesterolemia, familial, due to LDLR defect, modifier of, 143890"],"mode_of_inheritance":"","tags":[],"panel":{"id":6,"hash_id":"561518be22c1fc212900fb84","name":"Familial hypercholesterolaemia","disease_group":"Cardiovascular disorders","disease_sub_group":"Arteriopathies","status":"public","version":"1.26","version_created":"2019-10-07T15:50:14.542064Z","relevant_disorders":["Familial Hypercholesterolaemia","Familial Hypercholesterolemia"],"stats":{"number_of_genes":43,"number_of_strs":0,"number_of_regions":0},"types":[{"name":"Rare Disease 100K","slug":"rare-disease-100k","description":"Rare Disease 100K"}]}}]}