{"count":1,"next":null,"previous":null,"results":[{"gene_data":{"alias":["TAPA"],"biotype":"protein_coding","hgnc_id":"HGNC:11566","gene_name":"TAP binding protein","omim_gene":["601962"],"alias_name":["tapasin"],"gene_symbol":"TAPBP","hgnc_symbol":"TAPBP","hgnc_release":"2017-11-03","ensembl_genes":{"GRch37":{"82":{"location":"6:33267471-33282164","ensembl_id":"ENSG00000231925"}},"GRch38":{"90":{"location":"6:33299694-33314387","ensembl_id":"ENSG00000231925"}}},"hgnc_date_symbol_changed":"1997-12-17"},"entity_type":"gene","entity_name":"TAPBP","confidence_level":"2","penetrance":null,"mode_of_pathogenicity":null,"publications":["12149238"],"evidence":["Expert Review Amber","IUIS Classification February 2018","Victorian Clinical Genetics Services","ESID Registry 20171117","GRID V2.0","GOSH PID v.8.0"],"phenotypes":["Bare lymphocyte syndrome, type I 604571","HLA class I deficiency","Vasculitis, pyoderma gangrenosum","Immunodeficiencies affecting cellular and humoral immunity"],"mode_of_inheritance":"BIALLELIC, autosomal or pseudoautosomal","tags":["deletions"],"panel":{"id":398,"hash_id":null,"name":"Primary immunodeficiency","disease_group":"","disease_sub_group":"","status":"public","version":"1.132","version_created":"2019-09-27T14:37:49.085568Z","relevant_disorders":["Primary immunodeficiency disorders","A- or hypo-gammaglobulinaemia","Congenital neutropaenia","Agranulocytosis","Combined B and T cell defect","Inherited complement deficiency","SCID","Primary immune disorder","Primary immunodeficiency","A-gammaglobulinaemia","Agammaglobulinaemia","hypo-gammaglobulinaemia","hypogammaglobulinemia","immune deficiency syndromes","Severe combined immunodeficiency","Congenital neutopenia","Familial haemophagocytic lymphohistiocytic disorders","Familial hemophagocytic lymphohistiocytic disorders","PID","Sepsis","Disseminated non-tuberculous mycobacterial infection","R15"],"stats":{"number_of_genes":395,"number_of_strs":0,"number_of_regions":2},"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."}]}}]}