Vascular Occlusion Gene Set

Dataset DisGeNET Gene-Disease Associations
Category disease or phenotype associations
Type disease
External Link https://www.disgenet.org/browser/0/1/0/C1096458
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Genes

30 genes associated with the disease Vascular Occlusion in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.

Symbol Name
BMPR2 bone morphogenetic protein receptor, type II (serine/threonine kinase)
CCL2 chemokine (C-C motif) ligand 2
CRP C-reactive protein, pentraxin-related
CTNNB1 catenin (cadherin-associated protein), beta 1, 88kDa
EDN1 endothelin 1
EPO erythropoietin
FLT1 fms-related tyrosine kinase 1
FZD9 frizzled class receptor 9
GDNF glial cell derived neurotrophic factor
HK2 hexokinase 2
IGF1 insulin-like growth factor 1 (somatomedin C)
MIP major intrinsic protein of lens fiber
MTHFR methylenetetrahydrofolate reductase (NAD(P)H)
P4HB prolyl 4-hydroxylase, beta polypeptide
PGF placental growth factor
PIK3CG phosphatidylinositol-4,5-bisphosphate 3-kinase, catalytic subunit gamma
PLAT plasminogen activator, tissue
PLAU plasminogen activator, urokinase
PPARGC1A peroxisome proliferator-activated receptor gamma, coactivator 1 alpha
PPBP pro-platelet basic protein (chemokine (C-X-C motif) ligand 7)
PROC protein C (inactivator of coagulation factors Va and VIIIa)
SCD stearoyl-CoA desaturase (delta-9-desaturase)
SELP selectin P (granule membrane protein 140kDa, antigen CD62)
SERPINE1 serpin peptidase inhibitor, clade E (nexin, plasminogen activator inhibitor type 1), member 1
SPIN1 spindlin 1
TGFB3 transforming growth factor, beta 3
THBS1 thrombospondin 1
TNF tumor necrosis factor
TYMS thymidylate synthetase
VEGFA vascular endothelial growth factor A