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FIXa variant [plasma membrane]
Stable Identifier
R-HSA-9670846
Type
Complex
Species
Homo sapiens
Compartment
plasma membrane
Synonyms
F9 variant with mutation in the heavy chain
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 IX causes hemophilia B (Homo sapiens)
Defective F9 variant does not activate FX (Homo sapiens)
FIXa variant:FVIIIa does not convert FX to the active FXa (Homo sapiens)
factor VIIIa:factor IXa variant [plasma membrane] (Homo sapiens)
FIXa variant [plasma membrane] (Homo sapiens)
Participants
components
12xCbxE-3D-F9(47-191) [plasma membrane]
(Homo sapiens)
F9(227-461) variant [plasma membrane]
(Homo sapiens)
Participates
as a component of
factor VIIIa:factor IXa variant [plasma membrane] (Homo sapiens)
Disease
Name
Identifier
Synonyms
hemophilia B
DOID:12259
factor IX deficiency, Congenital factor IX deficiency, deficiency, functional factor IX, Congenital factor IX disorder
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