abnormality of the common coagulation pathway Gene Set
Genes
17 genes associated with the abnormality of the common coagulation pathway phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
Symbol |
Name |
ANO6
|
anoctamin 6
|
F10
|
coagulation factor X
|
F13A1
|
coagulation factor XIII, A1 polypeptide
|
F13B
|
coagulation factor XIII, B polypeptide
|
F5
|
coagulation factor V (proaccelerin, labile factor)
|
FGA
|
fibrinogen alpha chain
|
FGB
|
fibrinogen beta chain
|
FGG
|
fibrinogen gamma chain
|
GGCX
|
gamma-glutamyl carboxylase
|
LMAN1
|
lectin, mannose-binding, 1
|
MCFD2
|
multiple coagulation factor deficiency 2
|
PRF1
|
perforin 1 (pore forming protein)
|
PTPN11
|
protein tyrosine phosphatase, non-receptor type 11
|
STX11
|
syntaxin 11
|
UNC13D
|
unc-13 homolog D (C. elegans)
|
VKORC1
|
vitamin K epoxide reductase complex, subunit 1
|
XIAP
|
X-linked inhibitor of apoptosis, E3 ubiquitin protein ligase
|