Abnormal Thrombosis Gene Set

Dataset DisGeNET Gene-Disease Associations
Category disease or phenotype associations
Type disease
Description Venous or arterial thrombosis (formation of blood clots) of spontaneous nature and which cannot be fully explained by acquired risk (e.g. atherosclerosis). (Human Phenotype Ontology, HP_0001977)
External Link https://www.disgenet.org/browser/0/1/0/C4025731
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Genes

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

Symbol Name
BMPR2 bone morphogenetic protein receptor, type II (serine/threonine kinase)
CFTR cystic fibrosis transmembrane conductance regulator (ATP-binding cassette sub-family C, member 7)
CTRC chymotrypsin C (caldecrin)
JAK2 Janus kinase 2
MPI mannose phosphate isomerase
MYH9 myosin, heavy chain 9, non-muscle
PROC protein C (inactivator of coagulation factors Va and VIIIa)
PRSS1 protease, serine, 1 (trypsin 1)
PRSS2 protease, serine, 2 (trypsin 2)
RFT1 RFT1 homolog (S. cerevisiae)
RHAG Rh-associated glycoprotein
SLC2A10 solute carrier family 2 (facilitated glucose transporter), member 10
SPINK1 serine peptidase inhibitor, Kazal type 1