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VWF I1568N multimer:VWF I1568N (764-1605) [extracellular region]
Stable Identifier
R-HSA-9852787
Type
Complex
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 I1568N multimer [extracellular region] (Homo sapiens)
VWF I1568N multimer:VWF I1568N (764-1605) [extracellular region] (Homo sapiens)
Participants
components
VWF I1568N (764-1605) [extracellular region]
(Homo sapiens)
x 24
VWF I1568N (764-2813) [extracellular region]
(Homo sapiens)
Participates
as a member of
Cleaved VWF I1568N multimer [extracellular region] (Homo sapiens)
Disease
Name
Identifier
Synonyms
blood platelet disease
DOID:2218
platelet disorder, Thrombocytopathy
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