{"count":1,"next":null,"previous":null,"results":[{"gene_data":{"alias":["CEAP1","DRAP","ALP56"],"biotype":"protein_coding","hgnc_id":"HGNC:934","gene_name":"beta-site APP-cleaving enzyme 2","omim_gene":["605668"],"alias_name":["memapsin 1"],"gene_symbol":"BACE2","hgnc_symbol":"BACE2","hgnc_release":"2017-11-03T00:00:00","ensembl_genes":{"GRch37":{"82":{"location":"21:42539728-42654445","ensembl_id":"ENSG00000182240"}},"GRch38":{"90":{"location":"21:41167801-41282518","ensembl_id":"ENSG00000182240"}}},"hgnc_date_symbol_changed":"2000-05-23"},"entity_type":"gene","entity_name":"BACE2","confidence_level":"1","penetrance":"Complete","mode_of_pathogenicity":"","publications":[],"evidence":["Expert Review Red","Other"],"phenotypes":["HSCR"],"mode_of_inheritance":"Unknown","tags":["watchlist"],"panel":{"id":63,"hash_id":"58c7f5008f620328d77ce70f","name":"Familial Hirschsprung Disease","disease_group":"Gastroenterological disorders","disease_sub_group":"Gastrointestinal disorders","status":"public","version":"1.6","version_created":"2019-06-20T15:11:10.292595Z","relevant_disorders":[],"stats":{"number_of_genes":62,"number_of_strs":0,"number_of_regions":0},"types":[{"name":"Rare Disease 100K","slug":"rare-disease-100k","description":"Rare Disease 100K"}]}}]}
