von Willebrand factor

Symbol

VWF (may also be known as: None)

Organism

Human

Description

The glycoprotein encoded by this gene functions as both an antihemophilic factor carrier and a platelet-vessel wall mediator in the blood coagulation system. It is crucial to the hemostasis process. Mutations in this gene or deficiencies in this protein result in von Willebrand's disease. An unprocessed pseudogene has been found on chromosome 22. [provided by RefSeq, Jul 2008]

Orthologs

SymbolSpecies
vwf Danio rerio
Vwf Mus musculus

Links to external resources

Changes associated with this gene

GO Terms

GO IDGO TermGO Category
GO:0001889 liver development biological_process
GO:0001890 placenta development biological_process
GO:0002576 platelet degranulation biological_process
GO:0007155 cell adhesion biological_process
GO:0007596 blood coagulation biological_process
GO:0007597 blood coagulation, intrinsic pathway biological_process
Show more GO terms