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Protein-coding gene in the species Homo sapiens

Platelet glycoprotein VI

Platelet glycoprotein VI
All data from the card 18
Aliases
GP6, BDPLT11, GPIV, GPVI, glycoprotein VI platelet
External IDs
OMIM: 605546; MGI: 1889810; GeneCards: GP6
PDB
Ortholog search: PDBe RCSB
Chr.
Chromosome 19 (human)
Band
19q13.42
End
55,038,264 bp
Chr.
Chromosome 7 (mouse)
Band
7|7 A1
End
4,400,743 bp
BioGPS
More reference expression data
Databases
NCBI: entry; OMA: entry
Species
Human
Entrez
51206
Ensembl
ENSG00000088053ENSG00000274050ENSG00000278670ENSG00000276211ENSG00000277439ENSG00000278316ENSG00000275633ENSG00000274566ENSG00000275931ENSG00000276065
UniProt
Q9HCN6
RefSeq (mRNA)
NM_016363NM_001083899NM_001256017
RefSeq (protein)
NP_001077368NP_001242946NP_057447
Location (UCSC)
Chr 19: 55.01 – 55.04 Mb

Platelet glycoprotein VI (GPVI) is a glycoprotein receptor for collagen which is expressed in platelets. In humans, glycoprotein VI is encoded by the GP6 gene. It was first cloned in 2000 by several groups including that of Martine Jandrot-Perrus from INSERM.

Function

GPVI is a 58-kD platelet membrane glycoprotein that plays a crucial role in the collagen-induced activation and aggregation of platelets. Upon injury to the vessel wall and subsequent damage to the endothelial lining, exposure of the subendothelial matrix to blood flow results in deposition of platelets. Collagen fibers are the most thrombogenic macromolecular components of the extracellular matrix, with collagen types I, III, and VI being the major forms found in blood vessels. Platelet interaction with collagen occurs as a 2-step procedure: (1) the initial adhesion to collagen is followed by (2) an activation step leading to platelet secretion, recruitment of additional platelets, and aggregation. In physiologic conditions, the resulting platelet plug is the initial hemostatic event limiting blood loss. However, exposure of collagen after rupture of atherosclerotic plaques is a major stimulus of thrombus formation associated with myocardial infarction or stroke.

Complete or partial deficiency of GPVI in humans is a rare condition presenting as a mild bleeding disorder.

Interactions

GPVI has been shown to interact with LYN.

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Text from Wikipedia, CC BY-SA 4.0 · Source article