selective iga deficiency disease Gene Set

Dataset GWASdb SNP-Disease Associations
Category disease or phenotype associations
Type disease
Description A selective immunoglobulin deficiency disease that is the result of a deficiency of immunoglobulin A (IgA), an antibody that protects against infections of the mucous membranes lining the mouth, airways, and digestive tract. (Human Disease Ontology, DOID_11701)
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25 genes associated with the disease selective iga deficiency disease in GWAS and other genetic association datasets from the GWASdb SNP-Disease Associations dataset.

Symbol Name Standardized Value
HLA-DQA1 major histocompatibility complex, class II, DQ alpha 1 2.32996
IFIH1 interferon induced with helicase C domain 1 1.52067
CLEC16A C-type lectin domain family 16, member A 1.28906
TNFSF13 tumor necrosis factor (ligand) superfamily, member 13 1.26953
DGKZ diacylglycerol kinase, zeta 1.14463
FAS Fas cell surface death receptor 1.02476
FOXP1 forkhead box P1 0.898875
DOT1L DOT1-like histone H3K79 methyltransferase 0.892579
CD86 CD86 molecule 0.874542
NRP1 neuropilin 1 0.835629
RFC3 replication factor C (activator 1) 3, 38kDa 0.819144
MTCL1 microtubule crosslinking factor 1 0.804621
LOC440600 uncharacterized LOC440600 0.804621
ITGB2 integrin, beta 2 (complement component 3 receptor 3 and 4 subunit) 0.801304
ECT2L epithelial cell transforming 2 like 0.775452
IRF8 interferon regulatory factor 8 0.772631
DRD2 dopamine receptor D2 0.764084
ST6GALNAC3 ST6 (alpha-N-acetyl-neuraminyl-2,3-beta-galactosyl-1,3)-N-acetylgalactosaminide alpha-2,6-sialyltransferase 3 0.738669
GDE1 glycerophosphodiester phosphodiesterase 1 0.734059
PTPDC1 protein tyrosine phosphatase domain containing 1 0.724858
RAC2 ras-related C3 botulinum toxin substrate 2 (rho family, small GTP binding protein Rac2) 0.718432
AHI1 Abelson helper integration site 1 0.714351
PLCB1 phospholipase C, beta 1 (phosphoinositide-specific) 0.69773
CELF1 CUGBP, Elav-like family member 1 0.689554
MAP6D1 MAP6 domain containing 1 0.683452