Retinal Neovascularization Gene Set

Dataset HuGE Navigator Gene-Phenotype Associations
Category disease or phenotype associations
Type phenotype
Description formation of new blood vessels originating from the retinal veins and extending along the inner (vitreal) surface of the retina (Mammalian Phenotype Ontology, MP_0008852)
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Genes

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

Symbol Name
ADORA2A adenosine A2a receptor
ARMS2 age-related maculopathy susceptibility 2
C9 complement component 9
CFB complement factor B
CFH complement factor H
F5 coagulation factor V (proaccelerin, labile factor)
FLT1 fms-related tyrosine kinase 1
FZD4 frizzled class receptor 4
HTRA1 HtrA serine peptidase 1
IFNG interferon, gamma
KDR kinase insert domain receptor
LRP5 low density lipoprotein receptor-related protein 5
PON1 paraoxonase 1
TCF7L2 transcription factor 7-like 2 (T-cell specific, HMG-box)
VASH1 vasohibin 1
VEGFA vascular endothelial growth factor A