abnormality of the intrinsic pathway Gene Set

Dataset GWASdb SNP-Phenotype Associations
Category disease or phenotype associations
Type phenotype
Description An abnormality of the intrinsic pathway (also known as the contact activation pathway) of the coagulation cascade. (Human Phenotype Ontology, HP_0010989)
External Link http://jjwanglab.org/gwasdb/gwasdb2/gwasdb2/go_trait/HP:0010989
Similar Terms
Downloads & Tools

Genes

15 genes associated with the abnormality of the intrinsic pathway phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset.

Symbol Name Standardized Value
ABO ABO blood group (transferase A, alpha 1-3-N-acetylgalactosaminyltransferase; transferase B, alpha 1-3-galactosyltransferase) 3.17266
PROCR protein C receptor, endothelial 2.34964
SURF4 surfeit 4 2.3439
STXBP5 syntaxin binding protein 5 (tomosyn) 2.05673
VWF von Willebrand factor 1.76413
SURF2 surfeit 2 0.915998
EPB41L4A erythrocyte membrane protein band 4.1 like 4A 0.424122
ASIC2 acid sensing (proton gated) ion channel 2 0.413807
STAB2 stabilin 2 0.410331
ANKRD6 ankyrin repeat domain 6 0.406588
CDH2 cadherin 2, type 1, N-cadherin (neuronal) 0.405267
VAV2 vav 2 guanine nucleotide exchange factor 0.403073
ESR1 estrogen receptor 1 0.394651
DBH dopamine beta-hydroxylase (dopamine beta-monooxygenase) 0.391869
NRG1 neuregulin 1 0.387897