Qualitative Abnormality Of Granulocyte Gene Set

Dataset DisGeNET Gene-Disease Associations
Category disease or phenotype associations
Type disease
External Link https://www.disgenet.org/browser/0/1/0/C0272183
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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