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GP5 (gene)

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Protein-coding gene in the species Homo sapiens This article is about the glycoprotein V. For the GP5 computer chip, see GP5 chip. For the Soviet-era civilian gas mask, see GP-5 gas mask.
GP5
Identifiers
AliasesGP5, CD42d, GPV, glycoprotein V platelet
External IDsOMIM: 173511; MGI: 1096363; HomoloGene: 74523; GeneCards: GP5; OMA:GP5 - orthologs
Gene location (Human)
Chromosome 3 (human)
Chr.Chromosome 3 (human)
Chromosome 3 (human)Genomic location for GP5Genomic location for GP5
Band3q29Start194,394,821 bp
End194,399,266 bp
Gene location (Mouse)
Chromosome 16 (mouse)
Chr.Chromosome 16 (mouse)
Chromosome 16 (mouse)Genomic location for GP5Genomic location for GP5
Band16|16 B2Start30,126,503 bp
End30,129,597 bp
RNA expression pattern
Bgee
HumanMouse (ortholog)
Top expressed in
  • monocyte

  • trabecular bone

  • right uterine tube

  • bronchial epithelial cell

  • granulocyte

  • lymph node

  • blood

  • appendix

  • bone marrow

  • gallbladder
Top expressed in
  • tibiofemoral joint

  • blood

  • morula

  • blastocyst

  • embryo

  • spleen

  • embryo

  • yolk sac

  • abdominal wall

  • bone marrow
More reference expression data
BioGPS
More reference expression data
Gene ontology
Molecular function
Cellular component
Biological process
Sources:Amigo / QuickGO
Orthologs
SpeciesHumanMouse
Entrez

2814

14729

Ensembl

ENSG00000178732

ENSMUSG00000047953

UniProt

P40197

O08742
Q9QZU3

RefSeq (mRNA)

NM_004488

NM_008148

RefSeq (protein)

NP_004479

NP_032174

Location (UCSC)Chr 3: 194.39 – 194.4 MbChr 16: 30.13 – 30.13 Mb
PubMed search
Wikidata
View/Edit HumanView/Edit Mouse

Glycoprotein V (platelet) (GP5) also known as CD42d (Cluster of Differentiation 42d), is a human gene.

Human platelet glycoprotein V (GP5) is a part of the Ib-V-IX system of surface glycoproteins that constitute the receptor for von Willebrand factor (VWF; MIM 193400) and mediate the adhesion of platelets to injured vascular surfaces in the arterial circulation, a critical initiating event in hemostasis. The main portion of the receptor is a heterodimer composed of 2 polypeptide chains, an alpha chain (GP1BA; MIM 606672) and a beta chain (GP1BB; MIM 138720), that are linked by disulfide bonds. The complete receptor complex includes noncovalent association of the alpha and beta subunits with platelet glycoprotein IX (GP9; MIM 173515) and GP5. Mutations in GP1BA, GP1BB, and GP9 have been shown to cause Bernard-Soulier syndrome (MIM 231200), a bleeding disorder.

See also

References

  1. ^ GRCh38: Ensembl release 89: ENSG00000178732Ensembl, May 2017
  2. ^ GRCm38: Ensembl release 89: ENSMUSG00000047953Ensembl, May 2017
  3. "Human PubMed Reference:". National Center for Biotechnology Information, U.S. National Library of Medicine.
  4. "Mouse PubMed Reference:". National Center for Biotechnology Information, U.S. National Library of Medicine.
  5. ^ "Entrez Gene: GP5 glycoprotein V (platelet)".

Further reading

External links

This article incorporates text from the United States National Library of Medicine, which is in the public domain.

Proteins: clusters of differentiation (see also list of human clusters of differentiation)
1–50
51–100
101–150
151–200
201–250
251–300
301–350


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