Qualitative Abnormality Of Granulocyte Gene Set
Genes
20 genes associated with the disease Qualitative Abnormality Of Granulocyte in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
| Symbol |
Name |
|
ACTB
|
actin, beta
|
|
ADAM17
|
ADAM metallopeptidase domain 17
|
|
C5AR1
|
complement component 5a receptor 1
|
|
DOCK2
|
dedicator of cytokinesis 2
|
|
ELK3
|
ELK3, ETS-domain protein (SRF accessory protein 2)
|
|
EPHB1
|
EPH receptor B1
|
|
ESR1
|
estrogen receptor 1
|
|
G6PC
|
glucose-6-phosphatase, catalytic subunit
|
|
G6PC3
|
glucose 6 phosphatase, catalytic, 3
|
|
GABPA
|
GA binding protein transcription factor, alpha subunit 60kDa
|
|
HIF1A
|
hypoxia inducible factor 1, alpha subunit (basic helix-loop-helix transcription factor)
|
|
HMGB1
|
high mobility group box 1
|
|
HMOX1
|
heme oxygenase 1
|
|
NFE2L2
|
nuclear factor, erythroid 2-like 2
|
|
POTEF
|
POTE ankyrin domain family, member F
|
|
RAC2
|
ras-related C3 botulinum toxin substrate 2 (rho family, small GTP binding protein Rac2)
|
|
SLC37A4
|
solute carrier family 37 (glucose-6-phosphate transporter), member 4
|
|
SLC6A2
|
solute carrier family 6 (neurotransmitter transporter), member 2
|
|
SOD2
|
superoxide dismutase 2, mitochondrial
|
|
WDR1
|
WD repeat domain 1
|