Reactome | GP1BA variant [plasma membrane]

GP1BA variant [plasma membrane]

Stable Identifier

R-HSA-9844268

Type

Set [DefinedSet]

Species

Homo sapiens

Compartment

plasma membrane

Locations in the PathwayBrowser

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Disease (Homo sapiens)

- Diseases of hemostasis (Homo sapiens)
  - Defects of platelet adhesion to exposed collagen (Homo sapiens)
    - Enhanced binding of GP1BA variant to VWF multimer:collagen (Homo sapiens)
      - GP1BA variant binds to VWF multimer:collagen (Homo sapiens)
        
        Collagen type I fibril:VWF multimer:GP1BA variant:GP1BB:GP9:GP5 [plasma membrane] (Homo sapiens)
        
        GP1BA variant:GP1BB:GP9:GP5 [plasma membrane] (Homo sapiens)
        
        GP1BA variant:GP1BB:GP9 [plasma membrane] (Homo sapiens)
        
        GP1BA variant [plasma membrane] (Homo sapiens)
        
        GP1BA variant:GP1BB:GP9:GP5 [plasma membrane] (Homo sapiens)
        
        GP1BA variant:GP1BB:GP9 [plasma membrane] (Homo sapiens)
        
        GP1BA variant [plasma membrane] (Homo sapiens)

Participants

members

Participates

as a component of

GP1BA variant:GP1BB:GP9 [plasma membrane] (Homo sapiens)

Disease

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

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