IgA Deficiency Gene Set

Dataset HuGE Navigator Gene-Phenotype Associations
Category disease or phenotype associations
Type phenotype
Description A B cell deficiency that is an autosomal recessive disorder caused by mutation in the IgA (CD79 alpha) antigen receptor. (Human Disease Ontology, DOID_0060025)
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Genes

20 genes associated with the IgA Deficiency phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset.

Symbol Name
CLEC16A C-type lectin domain family 16, member A
CTLA4 cytotoxic T-lymphocyte-associated protein 4
HLA-A major histocompatibility complex, class I, A
HLA-B major histocompatibility complex, class I, B
HLA-DQA1 major histocompatibility complex, class II, DQ alpha 1
HLA-DQB1 major histocompatibility complex, class II, DQ beta 1
HLA-DRA major histocompatibility complex, class II, DR alpha
HLA-DRB1 major histocompatibility complex, class II, DR beta 1
ICOS inducible T-cell co-stimulator
IFIH1 interferon induced with helicase C domain 1
IGHA1 immunoglobulin heavy constant alpha 1
IL10 interleukin 10
IL6 interleukin 6
MSH5 mutS homolog 5
PRDM1 PR domain containing 1, with ZNF domain
PTPN22 protein tyrosine phosphatase, non-receptor type 22 (lymphoid)
TLR3 toll-like receptor 3
TNF tumor necrosis factor
TNFRSF13B tumor necrosis factor receptor superfamily, member 13B
XBP1 X-box binding protein 1