VASP (Vasodilator-Stimulated Phosphoprotein)

Actin cytoskeleton regulator and cell adhesion modulator

Gene Information Card

Symbol VASP
Full Name Vasodilator-stimulated phosphoprotein
Gene Type Protein coding
Chromosomal Location 19q13.32
NCBI Gene ID 7408 ncbi.nlm.nih.gov/gene/7408
Ensembl ID ENSG00000100263
UniProt ID P50552
OMIM ID 601617
HGNC ID 12652
Aliases VASP

Description

VASP (vasodilator-stimulated phosphoprotein) is a member of the Ena/VASP family of actin-associated proteins. It regulates actin filament dynamics, cell adhesion, and cell migration. VASP localizes to focal adhesions, lamellipodia, and filopodia, and is involved in platelet aggregation, endothelial barrier function, and cancer cell invasion. Its activity is modulated by phosphorylation via cAMP- and cGMP-dependent protein kinases.

Disease Associations

Disease category Pathophysiological mechanism Genomic evidence
Colorectal cancer Altered VASP expression and phosphorylation affect cell migration and invasion; overexpression correlates with poor prognosis. COSMIC; PMID: 21573173
Breast cancer VASP overexpression promotes metastasis through enhanced actin dynamics and focal adhesion turnover. COSMIC; PMID: 23431263
Cardiovascular disease VASP phosphorylation status is a marker of platelet inhibition; dysregulation linked to thrombosis and atherosclerosis. ClinVar; PMID: 15598816
Inflammatory bowel disease VASP expression changes in intestinal epithelium may contribute to barrier dysfunction. OMIM; PMID: 20628086

Expression Profile

Tissue Expression
Tissue nTPM level
Blood 12.2 Medium
Heart 8.5 Medium
Lung 10.1 Medium
Liver 6.3 Low
Kidney 9.8 Medium
Brain 7.4 Low
Colon 11.5 Medium
Breast 9.0 Medium
Cell Line Expression
Cell Line nTPM Notes
HeLa 14.3 Cervical cancer cell line
MCF7 11.8 Breast cancer cell line
A549 10.5 Lung cancer cell line
HCT116 13.1 Colorectal cancer cell line
HEK293 9.2 Embryonic kidney cell line
Data source:Human Protein Atlas(proteinatlas.org)

Mutations & Variants

Hotspot Mutations
Variant Type Frequency Functional Description
c.1A>G Missense <0.01% Likely benign; no functional data
c.103C>T Missense <0.01% Unknown significance
c.214G>A Missense <0.01% Unknown significance
c.340C>T Nonsense <0.01% Predicted loss of function
Mutation functional classification

Loss of Function (LOF)

Nonsense mutations (e.g., c.340C>T) are predicted to cause premature truncation and loss of actin-binding and regulatory functions.

Gain of Function (GOF)

No confirmed gain-of-function mutations reported in VASP.

Dominant Negative (DN)

No dominant-negative mutations described for VASP.

Gene Ontology (GO)

• actin binding • actin filament binding
• cell adhesion • cell migration
• focal adhesion assembly • lamellipodium assembly
• filopodium assembly • platelet aggregation
• signal transduction • protein phosphorylation

Pathways

cGMP-PKG signaling pathway
cAMP-PKA signaling pathway
Focal adhesion
Regulation of actin cytoskeleton
Platelet activation

Protein Summary

VASP is a 380-amino-acid protein (UniProt P50552) that contains an N-terminal Ena/VASP homology 1 (EVH1) domain, a central proline-rich region, and a C-terminal EVH2 domain. The EVH1 domain mediates binding to focal adhesion proteins such as zyxin and vinculin. The EVH2 domain binds actin and promotes filament elongation. Phosphorylation at Ser157, Ser239, and Thr278 by PKA and PKG regulates its localization and activity. VASP is widely expressed and plays key roles in cell motility, adhesion, and platelet function.

Related Products

Product name Cat.No. Species Gene ID
VASP Knockout HEK293 Cell Line EDJ-KQ760 Human 7408 Details Get a Quote
VASP Knockout A-549 Cell Line EDJ-KQ20776 Human 7408 Details Get a Quote
VASP Knockout HCT 116 Cell Line EDJ-KQ20778 Human 7408 Details Get a Quote
VASP Knockout HeLa Cell Line EDJ-KQ20779 Human 7408 Details Get a Quote
Displaying Records 1 To 4 Of 4 Records
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