{"count":1,"next":null,"previous":null,"results":[{"gene_data":{"alias":["HN3","PROS26"],"biotype":"protein_coding","hgnc_id":"HGNC:9541","gene_name":"proteasome subunit beta 4","omim_gene":["602177"],"alias_name":null,"gene_symbol":"PSMB4","hgnc_symbol":"PSMB4","hgnc_release":"2017-11-03","ensembl_genes":{"GRch37":{"82":{"location":"1:151372010-151374420","ensembl_id":"ENSG00000159377"}},"GRch38":{"90":{"location":"1:151399534-151401944","ensembl_id":"ENSG00000159377"}}},"hgnc_date_symbol_changed":"1995-05-03"},"entity_type":"gene","entity_name":"PSMB4","confidence_level":"2","penetrance":null,"mode_of_pathogenicity":null,"publications":["26524591"],"evidence":["Expert Review Amber","North West GLH","London North GLH","NHS GMS","Victorian Clinical Genetics Services"],"phenotypes":["CANDLE syndrome (Autoinflammation, lipodystrophy, and dermatosis syndrome)"],"mode_of_inheritance":"BIALLELIC, autosomal or pseudoautosomal","tags":["digenic"],"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."}]}}]}