Retinal Vein Occlusion Gene Set

Dataset HuGE Navigator Gene-Phenotype Associations
Category disease or phenotype associations
Type phenotype
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Genes

30 genes associated with the Retinal Vein Occlusion phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset.

Symbol Name
ACE angiotensin I converting enzyme
CCL2 chemokine (C-C motif) ligand 2
CCL5 chemokine (C-C motif) ligand 5
CXCL8 chemokine (C-X-C motif) ligand 8
F12 coagulation factor XII (Hageman factor)
F13A1 coagulation factor XIII, A1 polypeptide
F2 coagulation factor II (thrombin)
F5 coagulation factor V (proaccelerin, labile factor)
F8 coagulation factor VIII, procoagulant component
FGB fibrinogen beta chain
FTCD formimidoyltransferase cyclodeaminase
HPSE heparanase
IL10 interleukin 10
IL18 interleukin 18
IL1B interleukin 1, beta
IL1RN interleukin 1 receptor antagonist
IL4 interleukin 4
IL6 interleukin 6
ITGA2 integrin, alpha 2 (CD49B, alpha 2 subunit of VLA-2 receptor)
ITGA2B integrin, alpha 2b (platelet glycoprotein IIb of IIb/IIIa complex, antigen CD41)
ITGB3 integrin, beta 3 (platelet glycoprotein IIIa, antigen CD61)
MMP2 matrix metallopeptidase 2
MTHFR methylenetetrahydrofolate reductase (NAD(P)H)
PLAT plasminogen activator, tissue
PON1 paraoxonase 1
PROCR protein C receptor, endothelial
SERPINE1 serpin peptidase inhibitor, clade E (nexin, plasminogen activator inhibitor type 1), member 1
TIMP2 TIMP metallopeptidase inhibitor 2
TNF tumor necrosis factor
VKORC1 vitamin K epoxide reductase complex, subunit 1