{"count":1,"next":null,"previous":null,"results":[{"gene_data":{"alias":["MCH4"],"biotype":"protein_coding","hgnc_id":"HGNC:1500","gene_name":"caspase 10","omim_gene":["601762"],"alias_name":null,"gene_symbol":"CASP10","hgnc_symbol":"CASP10","hgnc_release":"2017-11-03","ensembl_genes":{"GRch37":{"82":{"location":"2:202047604-202094129","ensembl_id":"ENSG00000003400"}},"GRch38":{"90":{"location":"2:201182881-201229406","ensembl_id":"ENSG00000003400"}}},"hgnc_date_symbol_changed":"1997-04-21"},"entity_type":"gene","entity_name":"CASP10","confidence_level":"3","penetrance":null,"mode_of_pathogenicity":null,"publications":["25663566","21447005","10412980","16446975","9028957","16611303"],"evidence":["NHS GMS","North West GLH","London North GLH","IUIS Classification February 2018","Victorian Clinical Genetics Services","Expert Review Green","ESID Registry 20171117","GRID V2.0","GOSH PID v.8.0"],"phenotypes":["Autoimmune lymphoproliferative syndrome, type II, 603909","Autoimmune lymphoproliferative syndrome (ALPS)","Adenopathies, splenomegaly, autoimmunity","Diseases of Immune Dysregulation"],"mode_of_inheritance":"MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown","tags":[],"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."}]}}]}