igg deficiency Gene Set

Dataset HPO Gene-Disease Associations
Category disease or phenotype associations
Type phenotype
Description An abnormally decreased level of immunoglobulin IgG in blood. (Human Phenotype Ontology, HP_0004315)
External Link http://compbio.charite.de/hpoweb/showterm?id=HP:0004315
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26 genes associated with the igg deficiency phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

Symbol Name
AICDA activation-induced cytidine deaminase
ATM ATM serine/threonine kinase
B2M beta-2-microglobulin
BLM Bloom syndrome, RecQ helicase-like
CD40 CD40 molecule, TNF receptor superfamily member 5
CD40LG CD40 ligand
CNBP CCHC-type zinc finger, nucleic acid binding protein
CXCR4 chemokine (C-X-C motif) receptor 4
EPG5 ectopic P-granules autophagy protein 5 homolog (C. elegans)
ERCC2 excision repair cross-complementation group 2
ERCC3 excision repair cross-complementation group 3
GTF2H5 general transcription factor IIH, polypeptide 5
ICOS inducible T-cell co-stimulator
IKBKG inhibitor of kappa light polypeptide gene enhancer in B-cells, kinase gamma
IL2RG interleukin 2 receptor, gamma
ITK IL2-inducible T-cell kinase
PMM2 phosphomannomutase 2
RAG1 recombination activating gene 1
RAG2 recombination activating gene 2
RNF168 ring finger protein 168, E3 ubiquitin protein ligase
SH2D1A SH2 domain containing 1A
SP110 SP110 nuclear body protein
TCN2 transcobalamin II
TNFRSF13B tumor necrosis factor receptor superfamily, member 13B
TNFRSF13C tumor necrosis factor receptor superfamily, member 13C
UNG uracil-DNA glycosylase