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Cleaved VWF G1631D multimer [extracellular region]
Stable Identifier
R-HSA-9852784
Type
Set [DefinedSet]
Species
Homo sapiens
Compartment
extracellular region
Locations in the PathwayBrowser
Expand all
Disease (Homo sapiens)
Diseases of hemostasis (Homo sapiens)
Defects of platelet adhesion to exposed collagen (Homo sapiens)
Enhanced cleavage of VWF variant by ADAMTS13 (Homo sapiens)
ADAMTS13 cleaves VWF variant multimer (Homo sapiens)
Collagen type I fibril:cleaved VWF variant multimer [extracellular region] (Homo sapiens)
Cleaved VWF variants with increased susceptibility to proteolysis [extracellular region] (Homo sapiens)
Cleaved VWF G1631D multimer [extracellular region] (Homo sapiens)
Participants
members
VWF G1631D multimer:VWF G1631D (1606-2813) [extracellular region]
(Homo sapiens)
VWF G1631 multimer:VWF (764-1605) [extracellular region]
(Homo sapiens)
Participates
as a member of
Cleaved VWF variants with increased susceptibility to proteolysis [extracellular region] (Homo sapiens)
Disease
Name
Identifier
Synonyms
blood platelet disease
DOID:2218
platelet disorder, Thrombocytopathy
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