{"count":1,"next":null,"previous":null,"results":[{"gene_data":{"alias":["MST1","KRS2","YSK3"],"biotype":"protein_coding","hgnc_id":"HGNC:11408","gene_name":"serine/threonine kinase 4","omim_gene":["604965"],"alias_name":["mammalian sterile 20-like 1","yeast Ste20-like","kinase responsive to stress 2"],"gene_symbol":"STK4","hgnc_symbol":"STK4","hgnc_release":"2017-11-03","ensembl_genes":{"GRch37":{"82":{"location":"20:43595115-43708600","ensembl_id":"ENSG00000101109"}},"GRch38":{"90":{"location":"20:44966474-45079959","ensembl_id":"ENSG00000101109"}}},"hgnc_date_symbol_changed":"1997-10-09"},"entity_type":"gene","entity_name":"STK4","confidence_level":"3","penetrance":null,"mode_of_pathogenicity":null,"publications":["22174160","22294732","26801501","26117625","24453252"],"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","Combined B and T cell defect v1.12"],"phenotypes":["Hypergammaglobulinaemia, lymphopenia, combined immunodeficiency, congenital heart disease, autoimmunity","T-cell immunodeficiency, recurrent infections, autoimmunity, and cardiac malformations","AR hyperimmunoglobulin E syndrome","Combined immunodeficiency","Intermittent neutropenia, bacterial, viral (HPV), candidal infections, EBV lymphoproliferation, autoimmune cytopenias, lymphoma, congenital heart disease","Immunodeficiencies affecting cellular and humoral immunity"],"mode_of_inheritance":"BIALLELIC, autosomal or pseudoautosomal","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."}]}}]}