Prothrombin G20210A Mutation Gene Set
Genes
19 genes associated with the disease Prothrombin G20210A Mutation in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
| Symbol |
Name |
|
ACE
|
angiotensin I converting enzyme
|
|
ANAPC1
|
anaphase promoting complex subunit 1
|
|
COX8A
|
cytochrome c oxidase subunit VIIIA (ubiquitous)
|
|
CPB2
|
carboxypeptidase B2 (plasma)
|
|
F2
|
coagulation factor II (thrombin)
|
|
F5
|
coagulation factor V (proaccelerin, labile factor)
|
|
F8
|
coagulation factor VIII, procoagulant component
|
|
FGB
|
fibrinogen beta chain
|
|
G6PD
|
glucose-6-phosphate dehydrogenase
|
|
HRG
|
histidine-rich glycoprotein
|
|
IL31RA
|
interleukin 31 receptor A
|
|
ITGB3
|
integrin, beta 3 (platelet glycoprotein IIIa, antigen CD61)
|
|
LPA
|
lipoprotein, Lp(a)
|
|
MTHFR
|
methylenetetrahydrofolate reductase (NAD(P)H)
|
|
PROS1
|
protein S (alpha)
|
|
SCN5A
|
sodium channel, voltage gated, type V alpha subunit
|
|
SERPINB2
|
serpin peptidase inhibitor, clade B (ovalbumin), member 2
|
|
SERPINE1
|
serpin peptidase inhibitor, clade E (nexin, plasminogen activator inhibitor type 1), member 1
|
|
SLC25A24
|
solute carrier family 25 (mitochondrial carrier; phosphate carrier), member 24
|
