igm deficiency Gene Set
Genes
10 genes associated with the igm deficiency phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
| Symbol |
Name |
|
BLM
|
Bloom syndrome, RecQ helicase-like
|
|
CARD11
|
caspase recruitment domain family, member 11
|
|
CNBP
|
CCHC-type zinc finger, nucleic acid binding protein
|
|
ICOS
|
inducible T-cell co-stimulator
|
|
LAMTOR2
|
late endosomal/lysosomal adaptor, MAPK and MTOR activator 2
|
|
LRBA
|
LPS-responsive vesicle trafficking, beach and anchor containing
|
|
PLCG2
|
phospholipase C, gamma 2 (phosphatidylinositol-specific)
|
|
TCN2
|
transcobalamin II
|
|
TNFRSF13B
|
tumor necrosis factor receptor superfamily, member 13B
|
|
WAS
|
Wiskott-Aldrich syndrome
|
