VWF

GENE INFORMATION

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Gene name

VWF (HGNC Symbol)

Synonyms

F8VWF

Description

Von Willebrand factor (HGNC Symbol)

Entrez gene summary

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]

Chromosome

12

Cytoband

p13.31

Chromosome location (bp)

5948874 - 6124770

Protein evidence

Evidence at protein level (all genes)

Ensembl

ENSG00000110799 (version 78.38)

Entrez gene

7450

UniProt

P04275 (UniProt - Evidence at protein level)

neXtProt

NX_P04275

Antibodypedia

VWF antibodies
 

PROTEIN VIEW

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VWF-002
 
 
 
 
 

PROTEIN INFORMATION

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Splice variant

Ensembl

UniProt

Protein class

Gene ontology

Length
(aa)

Molecular mass
(kDa)

Signal peptide
(predicted)

Transmembrane regions
(predicted)

VWF-002 ENSP00000261405
ENST00000261405
P04275
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