Hypopigmentation-Immunodeficiency Disease Gene Set
Genes
14 genes associated with the disease Hypopigmentation-Immunodeficiency Disease in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
| Symbol |
Name |
|
AP3B1
|
adaptor-related protein complex 3, beta 1 subunit
|
|
DNAJC21
|
DnaJ (Hsp40) homolog, subfamily C, member 21
|
|
FCGR3A
|
Fc fragment of IgG, low affinity IIIa, receptor (CD16a)
|
|
FCGR3B
|
Fc fragment of IgG, low affinity IIIb, receptor (CD16b)
|
|
FGL1
|
fibrinogen-like 1
|
|
HPS1
|
Hermansky-Pudlak syndrome 1
|
|
MLPH
|
melanophilin
|
|
MYO5A
|
myosin VA (heavy chain 12, myoxin)
|
|
NCR3
|
natural cytotoxicity triggering receptor 3
|
|
ORAI1
|
ORAI calcium release-activated calcium modulator 1
|
|
RAB27A
|
RAB27A, member RAS oncogene family
|
|
RAB27B
|
RAB27B, member RAS oncogene family
|
|
SBF2
|
SET binding factor 2
|
|
VPS39
|
vacuolar protein sorting 39 homolog (S. cerevisiae)
|
