hypertensive retinopathy Gene Set

Dataset DISEASES Text-mining Gene-Disease Association Evidence Scores
Category disease or phenotype associations
Type disease
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Genes

23 genes co-occuring with the disease hypertensive retinopathy in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.

Symbol Name Standardized Value
PSMD9 proteasome (prosome, macropain) 26S subunit, non-ATPase, 9 1.13543
ALB albumin 0.97212
REN renin 0.952021
MBD1 methyl-CpG binding domain protein 1 0.885569
RING1 ring finger protein 1 0.779841
WDR20 WD repeat domain 20 0.72612
SELENBP1 selenium binding protein 1 0.661197
NTS neurotensin 0.617877
ACE angiotensin I converting enzyme 0.531154
WDFY2 WD repeat and FYVE domain containing 2 0.451831
HSD11B2 hydroxysteroid (11-beta) dehydrogenase 2 0.403064
F2R coagulation factor II (thrombin) receptor 0.392257
CYP11B2 cytochrome P450, family 11, subfamily B, polypeptide 2 0.368149
DNTT DNA nucleotidylexotransferase 0.360395
AGTR1 angiotensin II receptor, type 1 0.322637
FLNA filamin A, alpha 0.297291
LEPR leptin receptor 0.28151
ADAMTS13 ADAM metallopeptidase with thrombospondin type 1 motif, 13 0.222479
LEP leptin 0.214975
VEGFA vascular endothelial growth factor A 0.204263
XIAP X-linked inhibitor of apoptosis, E3 ubiquitin protein ligase 0.203275
APOH apolipoprotein H (beta-2-glycoprotein I) 0.199033
KDR kinase insert domain receptor 0.171036