iga deficiency Gene Set

Dataset GWASdb SNP-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)
External Link http://jjwanglab.org/gwasdb/gwasdb2/gwasdb2/go_trait/HP:0002720
Similar Terms
Downloads & Tools

Genes

6 genes associated with the iga deficiency phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset.

Symbol Name Standardized Value
NCK2 NCK adaptor protein 2 1.51005
NFASC neurofascin 1.48419
TNFSF13 tumor necrosis factor (ligand) superfamily, member 13 1.11203
CSMD1 CUB and Sushi multiple domains 1 0.509391
CHN2 chimerin 2 0.456563
LINC00547 long intergenic non-protein coding RNA 547 0.448846