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GENE INFORMATION

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Gene name

GP1BA (HGNC Symbol)

Synonyms

CD42b, GP1B

Description

glycoprotein Ib (platelet), alpha polypeptide (HGNC Symbol)

Entrez gene summary

Glycoprotein Ib (GP Ib) is a platelet surface membrane glycoprotein composed of a heterodimer, an alpha chain and a beta chain, that is linked by disulfide bonds. The Gp Ib functions as a receptor for von Willebrand factor (VWF). The complete receptor complex includes noncovalent association of the alpha and beta subunits with platelet glycoprotein IX and platelet glycoprotein V. The binding of the GP Ib-IX-V complex to VWF facilitates initial platelet adhesion to vascular subendothelium after vascular injury, and also initiates signaling events within the platelet that lead to enhanced platelet activation, thrombosis, and hemostasis. This gene encodes the alpha subunit. Several polymorphisms and mutations have been described in this gene, some of which are the cause of Bernard-Soulier syndromes and platelet-type von Willebrand disease. [provided by RefSeq, Mar 2010]

Chromosome

17 (Chromosome progress)

Cytoband

p13.2

Chromosome location (bp)

4835592 - 4838325

Ensembl

ENSG00000185245 (version 69.37)

Entrez gene

2811

UniProt

P07359

neXtProt

NX_P07359

Antibodypedia

GP1BA antibodies
 

PROTEIN VIEW

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GP1BA-001
 
 
 
 
 

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)

GP1BA-001 ENSP00000329380
ENST00000329125
P07359
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