iga deficiency Gene Set
Genes
16 genes associated with the iga 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
|
|
BLM
|
Bloom syndrome, RecQ helicase-like
|
|
CD40
|
CD40 molecule, TNF receptor superfamily member 5
|
|
CD40LG
|
CD40 ligand
|
|
CR2
|
complement component (3d/Epstein Barr virus) receptor 2
|
|
ICOS
|
inducible T-cell co-stimulator
|
|
IKBKG
|
inhibitor of kappa light polypeptide gene enhancer in B-cells, kinase gamma
|
|
IL2RA
|
interleukin 2 receptor, alpha
|
|
LRBA
|
LPS-responsive vesicle trafficking, beach and anchor containing
|
|
PLCG2
|
phospholipase C, gamma 2 (phosphatidylinositol-specific)
|
|
PMM2
|
phosphomannomutase 2
|
|
PTRF
|
polymerase I and transcript release factor
|
|
TCN2
|
transcobalamin II
|
|
TNFRSF13B
|
tumor necrosis factor receptor superfamily, member 13B
|
|
UNG
|
uracil-DNA glycosylase
|
