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VWF gene

von Willebrand factor

Key facts

Official symbol
VWF
Full name
VWF
Chromosome
12
Map location
12p13.31
Organism
Homo sapiens
NCBI Gene ID
7450
Also known as
F8VWF, VWD

Function summary

This gene encodes a glycoprotein involved in hemostasis. The encoded preproprotein is proteolytically processed following assembly into large multimeric complexes. These complexes function in the adhesion of platelets to sites of vascular injury and the transport of various proteins in the blood. Mutations in this gene result in von Willebrand disease, an inherited bleeding disorder. An unprocessed pseudogene has been found on chromosome 22. [provided by RefSeq, Oct 2015].

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Data source: NCBI Gene · alsesAI Gene Library