increased igm level Gene Set

Dataset HPO Gene-Disease Associations
Category disease or phenotype associations
Type phenotype
Description An abnormally increased level of immunoglobulin M in blood. (Human Phenotype Ontology, HP_0003496)
External Link http://compbio.charite.de/hpoweb/showterm?id=HP:0003496
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Genes

10 genes associated with the increased igm level phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

Symbol Name
CASP10 caspase 10, apoptosis-related cysteine peptidase
CD40 CD40 molecule, TNF receptor superfamily member 5
CD40LG CD40 ligand
FAS Fas cell surface death receptor
FASLG Fas ligand (TNF superfamily, member 6)
IKBKG inhibitor of kappa light polypeptide gene enhancer in B-cells, kinase gamma
KLHDC8B kelch domain containing 8B
MYD88 myeloid differentiation primary response 88
SH2D1A SH2 domain containing 1A
UNG uracil-DNA glycosylase