abnormality of prothrombin Gene Set

Dataset GWASdb SNP-Phenotype Associations
Category disease or phenotype associations
Type phenotype
Description An anomaly of clotting factor II, which is known as prothrombin, a vitamin K-dependent proenzyme that functions in the blood coagulation cascade. (Human Phenotype Ontology, HP_0012200)
External Link http://jjwanglab.org/gwasdb/gwasdb2/gwasdb2/go_trait/HP:0012200
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Genes

9 genes associated with the abnormality of prothrombin phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset.

Symbol Name Standardized Value
KNG1 kininogen 1 3.37991
HRG histidine-rich glycoprotein 3.07791
ABO ABO blood group (transferase A, alpha 1-3-N-acetylgalactosaminyltransferase; transferase B, alpha 1-3-galactosyltransferase) 2.99384
F7 coagulation factor VII (serum prothrombin conversion accelerator) 2.61302
F11 coagulation factor XI 2.48651
EDEM2 ER degradation enhancer, mannosidase alpha-like 2 1.58488
F5 coagulation factor V (proaccelerin, labile factor) 1.30781
AGBL1 ATP/GTP binding protein-like 1 1.18704
C6ORF10 chromosome 6 open reading frame 10 1.0674