Reactome | VWF C1099P multimer [extracellular region]

VWF C1099P multimer [extracellular region]

Stable Identifier

R-HSA-9844264

Type

Complex

Species

Homo sapiens

Compartment

extracellular region

Synonyms

VWF C1099P (764-2813) multimer, von Willibrand factor multimer

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:VWF variant multimer [extracellular region] (Homo sapiens)
        
        VWF variants with increased susceptibility to proteolysis [extracellular region] (Homo sapiens)
        
        VWF C1099P multimer [extracellular region] (Homo sapiens)

Participants

components

x 50 VWF C1099P (764-2813) [extracellular region] (Homo sapiens)

Participates

as a member of

VWF variants with increased susceptibility to proteolysis [extracellular region] (Homo sapiens)

Disease

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

Cross References

Mondo

0000009

© 2025 Reactome

Cite Us!