impaired ig class switch recombination Gene Set

Dataset HPO Gene-Disease Associations
Category disease or phenotype associations
Type phenotype
Description An impairment of the class-switch recombination process that normally leads B lymphocytes to produce IgG, IgA, or IgE. (Human Phenotype Ontology, HP_0002959)
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4 genes associated with the impaired ig class switch recombination phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

Symbol Name
AICDA activation-induced cytidine deaminase
CD40 CD40 molecule, TNF receptor superfamily member 5
CD40LG CD40 ligand
UNG uracil-DNA glycosylase