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factor VIIIa A1:A3-C1-C2 [extracellular region]
Stable Identifier
R-HSA-9670019
Type
Complex
Species
Homo sapiens
Compartment
extracellular region
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 F8 accelerates dissociation of the A2 domain (Homo sapiens)
Defects in F8 A2 domain accelerate dissociation of the A2 domain (Homo sapiens)
factor VIIIa A1:A3-C1-C2 [extracellular region] (Homo sapiens)
Hemostasis (Homo sapiens)
Formation of Fibrin Clot (Clotting Cascade) (Homo sapiens)
Intrinsic Pathway of Fibrin Clot Formation (Homo sapiens)
Factor VIIIa dissociates (Homo sapiens)
factor VIIIa A1:A3-C1-C2 [extracellular region] (Homo sapiens)
Participants
components
factor VIIIa A1 polypeptide [extracellular region]
(Homo sapiens)
factor VIIIa A3 C1 C2 polypeptide [extracellular region]
(Homo sapiens)
Participates
as an output of
Defects in F8 A2 domain accelerate dissociation of the A2 domain (Homo sapiens)
Factor VIIIa dissociates (Homo sapiens)
Inferred To
factor VIIIa A1:A3-C1-C2 [extracellular region]
(Bos taurus)
factor VIIIa A1:A3-C1-C2 [extracellular region]
(Gallus gallus)
factor VIIIa A1:A3-C1-C2 [extracellular region]
(Mus musculus)
factor VIIIa A1:A3-C1-C2 [extracellular region]
(Rattus norvegicus)
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