{"count":1,"next":null,"previous":null,"results":[{"gene_data":{"alias":["STAP-1","BRDG1"],"biotype":"protein_coding","hgnc_id":"HGNC:24133","gene_name":"signal transducing adaptor family member 1","omim_gene":["604298"],"alias_name":["BCR downstream signaling 1"],"gene_symbol":"STAP1","hgnc_symbol":"STAP1","hgnc_release":"2017-11-03T00:00:00","ensembl_genes":{"GRch37":{"82":{"location":"4:68424446-68473055","ensembl_id":"ENSG00000035720"}},"GRch38":{"90":{"location":"4:67558728-67607337","ensembl_id":"ENSG00000035720"}}},"hgnc_date_symbol_changed":"2007-08-09"},"entity_type":"gene","entity_name":"STAP1","confidence_level":"1","penetrance":"Complete","mode_of_pathogenicity":"","publications":["25035151","26036859","25170087"],"evidence":["Expert Review Red","Literature"],"phenotypes":["hypercholesterolemia"],"mode_of_inheritance":"MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted","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"}]}}]}