Dysgammaglobulinemia Gene Set

Dataset DisGeNET Gene-Disease Associations
Category disease or phenotype associations
Type disease
Description A selective immunoglobulin deficiency disease that is caused by a reduction in some types of gamma globulins. (Human Disease Ontology, DOID_11702)
External Link https://www.disgenet.org/browser/0/1/0/C0013374
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Genes

9 genes associated with the disease Dysgammaglobulinemia in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.

Symbol Name
APCS amyloid P component, serum
CD40LG CD40 ligand
IKBKG inhibitor of kappa light polypeptide gene enhancer in B-cells, kinase gamma
IKZF1 IKAROS family zinc finger 1 (Ikaros)
IL4 interleukin 4
MAGT1 magnesium transporter 1
NBN nibrin
SH2D1A SH2 domain containing 1A
XIAP X-linked inhibitor of apoptosis, E3 ubiquitin protein ligase