hypergammaglobulinemia Gene Set

Dataset HPO Gene-Disease Associations
Category disease or phenotype associations
Type phenotype
Description An increased level of gamma globulin (immunoglobulin) in the blood. (Human Phenotype Ontology, HP_0010702)
External Link http://compbio.charite.de/hpoweb/showterm?id=HP:0010702
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Genes

29 genes associated with the hypergammaglobulinemia phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

Symbol Name
ADA adenosine deaminase
CASP10 caspase 10, apoptosis-related cysteine peptidase
CD40 CD40 molecule, TNF receptor superfamily member 5
CD40LG CD40 ligand
CDSN corneodesmosin
COL1A1 collagen, type I, alpha 1
ELANE elastase, neutrophil expressed
FAS Fas cell surface death receptor
FASLG Fas ligand (TNF superfamily, member 6)
GBA glucosidase, beta, acid
IFIH1 interferon induced with helicase C domain 1
IKBKG inhibitor of kappa light polypeptide gene enhancer in B-cells, kinase gamma
KLHDC8B kelch domain containing 8B
KRT1 keratin 1, type II
KRT9 keratin 9, type I
MVK mevalonate kinase
MYD88 myeloid differentiation primary response 88
PSMB8 proteasome (prosome, macropain) subunit, beta type, 8
SCARB2 scavenger receptor class B, member 2
SETX senataxin
SFTPA2 surfactant protein A2
SH2D1A SH2 domain containing 1A
SPINK5 serine peptidase inhibitor, Kazal type 5
STAT3 signal transducer and activator of transcription 3 (acute-phase response factor)
TMEM173 transmembrane protein 173
TYK2 tyrosine kinase 2
UNG uracil-DNA glycosylase
VPS45 vacuolar protein sorting 45 homolog (S. cerevisiae)
WAS Wiskott-Aldrich syndrome