iga deficiency Gene Set

Dataset GAD Gene-Disease Associations
Category disease or phenotype associations
Type disease
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

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

Symbol Name
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-DRB1 major histocompatibility complex, class II, DR beta 1
IGHA1 immunoglobulin heavy constant alpha 1
IL10 interleukin 10
IL6 interleukin 6
MSH5 mutS homolog 5
TNFRSF13B tumor necrosis factor receptor superfamily, member 13B