Blood Coagulation Disorders, Inherited Gene Set

Dataset HuGE Navigator Gene-Phenotype Associations
Category disease or phenotype associations
Type phenotype
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Genes

20 genes associated with the Blood Coagulation Disorders, Inherited phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset.

Symbol Name
ABO ABO blood group (transferase A, alpha 1-3-N-acetylgalactosaminyltransferase; transferase B, alpha 1-3-galactosyltransferase)
ACE angiotensin I converting enzyme
APOB apolipoprotein B
APOE apolipoprotein E
CYP2C9 cytochrome P450, family 2, subfamily C, polypeptide 9
F12 coagulation factor XII (Hageman factor)
F13A1 coagulation factor XIII, A1 polypeptide
F2 coagulation factor II (thrombin)
F5 coagulation factor V (proaccelerin, labile factor)
FGB fibrinogen beta chain
GRK6 G protein-coupled receptor kinase 6
HRG histidine-rich glycoprotein
ITGB3 integrin, beta 3 (platelet glycoprotein IIIa, antigen CD61)
KLKB1 kallikrein B, plasma (Fletcher factor) 1
KNG1 kininogen 1
MTHFR methylenetetrahydrofolate reductase (NAD(P)H)
SERPINE1 serpin peptidase inhibitor, clade E (nexin, plasminogen activator inhibitor type 1), member 1
SLC19A2 solute carrier family 19 (thiamine transporter), member 2
THBD thrombomodulin
VKORC1 vitamin K epoxide reductase complex, subunit 1