Thromboembolism Gene Set

Dataset DisGeNET Gene-Disease Associations
Category disease or phenotype associations
Type disease
Description The formation of a blood clot inside a blood vessel that subsequently travels through the blood stream from the site where it formed to another location in the body, generally leading to vascular occlusion at the distant site. (Human Phenotype Ontology, HP_0001907)
External Link https://www.disgenet.org/browser/0/1/0/C1112433
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Genes

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

Symbol Name
ACTB actin, beta
ADA2 adenosine deaminase 2
ADORA2A adenosine A2a receptor
ASRGL1 asparaginase like 1
C1S complement component 1, s subcomponent
CHI3L1 chitinase 3-like 1 (cartilage glycoprotein-39)
CRP C-reactive protein, pentraxin-related
GPX3 glutathione peroxidase 3
KCNQ1 potassium channel, voltage gated KQT-like subfamily Q, member 1
PLAT plasminogen activator, tissue
ROCK2 Rho-associated, coiled-coil containing protein kinase 2
SERPINF1 serpin peptidase inhibitor, clade F (alpha-2 antiplasmin, pigment epithelium derived factor), member 1
SERPINF2 serpin peptidase inhibitor, clade F (alpha-2 antiplasmin, pigment epithelium derived factor), member 2