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