Hyper-Igm Immunodeficiency Syndrome Gene Set

Dataset DisGeNET Gene-Disease Associations
Category disease or phenotype associations
Type disease
External Link https://www.disgenet.org/browser/0/1/0/C1720956
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Genes

31 genes associated with the disease Hyper-Igm Immunodeficiency Syndrome in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.

Symbol Name
AICDA activation-induced cytidine deaminase
BTK Bruton agammaglobulinemia tyrosine kinase
CD19 CD19 molecule
CD27 CD27 molecule
CD40 CD40 molecule, TNF receptor superfamily member 5
CD40LG CD40 ligand
CD80 CD80 molecule
CHI3L1 chitinase 3-like 1 (cartilage glycoprotein-39)
CYBB cytochrome b-245, beta polypeptide
EBI3 Epstein-Barr virus induced 3
ERG v-ets avian erythroblastosis virus E26 oncogene homolog
FCER2 Fc fragment of IgE, low affinity II, receptor for (CD23)
FOXP3 forkhead box P3
HPRT1 hypoxanthine phosphoribosyltransferase 1
IKBKG inhibitor of kappa light polypeptide gene enhancer in B-cells, kinase gamma
IL10 interleukin 10
IL18R1 interleukin 18 receptor 1
IL2RA interleukin 2 receptor, alpha
ISG20 interferon stimulated exonuclease gene 20kDa
MRC1 mannose receptor, C type 1
MRFAP1 Morf4 family associated protein 1
NCF1 neutrophil cytosolic factor 1
PIK3CA phosphatidylinositol-4,5-bisphosphate 3-kinase, catalytic subunit alpha
PIK3CB phosphatidylinositol-4,5-bisphosphate 3-kinase, catalytic subunit beta
PIK3CD phosphatidylinositol-4,5-bisphosphate 3-kinase, catalytic subunit delta
PIK3CG phosphatidylinositol-4,5-bisphosphate 3-kinase, catalytic subunit gamma
PIK3R1 phosphoinositide-3-kinase, regulatory subunit 1 (alpha)
SWAP70 SWAP switching B-cell complex 70kDa subunit
TNF tumor necrosis factor
TRAP triiodothyronine receptor auxiliary protein
UNG uracil-DNA glycosylase