Reactome | VWF G1579R multimer:VWF G1579R (764-1605) [extracellular region]

VWF G1579R multimer:VWF G1579R (764-1605) [extracellular region]

Stable Identifier

R-HSA-9852779

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 G1579R multimer [extracellular region] (Homo sapiens)
        
        VWF G1579R multimer:VWF G1579R (764-1605) [extracellular region] (Homo sapiens)

Participants

components

Participates

as a member of

Cleaved VWF G1579R multimer [extracellular region] (Homo sapiens)

Disease

Name	Identifier	Synonyms
blood platelet disease	DOID:2218	platelet disorder, Thrombocytopathy

© 2024 Reactome

Cite Us!