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factor VIIIa variant [plasma membrane]
Stable Identifier
R-HSA-9668353
Type
Complex
Species
Homo sapiens
Compartment
plasma membrane
Synonyms
FVIIIa variant
Locations in the PathwayBrowser
Expand all
Disease (Homo sapiens)
Diseases of hemostasis (Homo sapiens)
Defects of contact activation system (CAS) and kallikrein/kinin system (KKS) (Homo sapiens)
Defective factor VIII causes hemophilia A (Homo sapiens)
Defective cofactor function of FVIIIa variant (Homo sapiens)
FVIIIa variant:FIXa does not convert FX to the active FXa (Homo sapiens)
FVIIIa variant:FIXa [plasma membrane] (Homo sapiens)
factor VIIIa variant [plasma membrane] (Homo sapiens)
Participants
components
F8(373-640) variant [plasma membrane]
(Homo sapiens)
factor VIIIa A1 polypeptide [plasma membrane]
(Homo sapiens)
factor VIIIa A3 C1 C2 polypeptide [plasma membrane]
(Homo sapiens)
Participates
as a component of
FVIIIa variant:FIXa [plasma membrane] (Homo sapiens)
Disease
Name
Identifier
Synonyms
factor VIII deficiency
DOID:12134
Congenital factor VIII disorder, Subhemophilia, Hemophilia A
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