retinopathy of prematurity Gene Set
Dataset
GAD Gene-Disease Associations
Category
disease or phenotype associations
Type
disease
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Genes
18 genes associated with the disease retinopathy of prematurity in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
Symbol
Name
ALDH2
aldehyde dehydrogenase 2 family (mitochondrial)
ANGPT2
angiopoietin 2
CFH
complement factor H
EPAS1
endothelial PAS domain protein 1
EPO
erythropoietin
ESR1
estrogen receptor 1
FZD4
frizzled class receptor 4
HIF1A
hypoxia inducible factor 1, alpha subunit (basic helix-loop-helix transcription factor)
IGF1
insulin-like growth factor 1 (somatomedin C)
IL1A
interleukin 1, alpha
IL1B
interleukin 1, beta
NDP
Norrie disease (pseudoglioma)
NOS3
nitric oxide synthase 3 (endothelial cell)
SERPINF1
serpin peptidase inhibitor, clade F (alpha-2 antiplasmin, pigment epithelium derived factor), member 1
TGFB1
transforming growth factor, beta 1
TNF
tumor necrosis factor
TRAF2
TNF receptor-associated factor 2
VEGFA
vascular endothelial growth factor A