von willebrand's disease Gene Set

Dataset GWASdb SNP-Disease Associations
Category disease or phenotype associations
Type disease
Description A coagulation protein disease that is a hereditary abnormality which slows the blood clotting process. It arises from a qualitative or quantitative deficiency of von Willebrand factor (vWF), a multimeric protein that is required for platelet adhesion. (Human Disease Ontology, DOID_12531)
External Link http://jjwanglab.org/gwasdb/gwasdb2/gwasdb2/go_trait/DOID:12531
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Genes

22 genes associated with the disease von willebrand's disease in GWAS and other genetic association datasets from the GWASdb SNP-Disease Associations dataset.

Symbol Name Standardized Value
F7 coagulation factor VII (serum prothrombin conversion accelerator) 4.56214
ABO ABO blood group (transferase A, alpha 1-3-N-acetylgalactosaminyltransferase; transferase B, alpha 1-3-galactosyltransferase) 2.94782
F10 coagulation factor X 2.85945
SURF4 surfeit 4 2.79765
HNF4A hepatocyte nuclear factor 4, alpha 2.39563
PROCR protein C receptor, endothelial 2.3744
GCKR glucokinase (hexokinase 4) regulator 2.2338
VWF von Willebrand factor 2.01663
SURF2 surfeit 2 1.61157
APOA5 apolipoprotein A-V 1.46277
ZPR1 ZPR1 zinc finger 1.27258
PRKCQ protein kinase C, theta 1.2606
BUD13 BUD13 homolog (S. cerevisiae) 1.22504
EPB41L4A erythrocyte membrane protein band 4.1 like 4A 1.19386
ASIC2 acid sensing (proton gated) ion channel 2 1.14463
STAB2 stabilin 2 1.10764
ANKRD6 ankyrin repeat domain 6 1.04846
CDH2 cadherin 2, type 1, N-cadherin (neuronal) 1.02476
VAV2 vav 2 guanine nucleotide exchange factor 0.986376
ESR1 estrogen receptor 1 0.869084
DBH dopamine beta-hydroxylase (dopamine beta-monooxygenase) 0.835629
NRG1 neuregulin 1 0.78889