GP1BA

GENERAL INFORMATION

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Gene name

GP1BA

Gene description

Glycoprotein Ib (platelet), alpha polypeptide

Protein class

CD markers
Disease related genes
Plasma proteins
Predicted membrane proteins

Predicted localization

Membrane

Number of transcripts

2
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HUMAN PROTEIN ATLAS INFORMATION

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RNA tissue category

HPA:Tissue enhanced (lymph node, tonsil)
GTEx:Mixed

Protein evidence

Evidence at protein level

Protein localization

Expression in platelets and in megakaryocytes.

ANTIBODY RELIABILITY

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Data reliability
description

Pending RNA-based expert annotation.

Data reliability

Supportive based on 2 antibodies.
HPA013316 , CAB002496
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RNA AND PROTEIN EXPRESSION SUMMARY

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RNA expression (FPKM) Protein expression (score)
Brain
Endocrine tissues
Bone marrow & immune system
Muscle tissues
Lung
Liver & gallbladder
Pancreas
Gastrointestinal tract
Kidney & urinary bladder
Male tissues
Female tissues
Adipose & soft tissue
Skin
Cerebral cortex

Bone marrow

Lymph node

Liver

Colon

Kidney

Testis



PROTEIN EXPRESSION OVERVIEW

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Organ

Expression



RNA EXPRESSION OVERVIEW

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HPA dataset
RNA tissue category:  Tissue enhanced (lymph node, tonsil)

Organ

Expression

GTEx dataset
RNA tissue category:  Mixed

Organ

Expression



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. Mutations in this gene result in Bernard-Soulier syndromes and platelet-type von Willebrand disease. The coding region of this gene is known to contain a polymophic variable number tandem repeat (VNTR) domain that is associated with susceptibility to nonarteritic anterior ischemic optic neuropathy. [provided by RefSeq, Oct 2013]

Chromosome

17

Cytoband

p13.2

Chromosome location (bp)

4932297 - 4935030

Protein evidence

Evidence at protein level (all genes)

Ensembl

ENSG00000185245 (version 78.38)

Entrez gene

2811

UniProt

P07359 (UniProt - Evidence at protein level)

neXtProt

NX_P07359

Antibodypedia

GP1BA antibodies


PROTEIN BROWSER

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ENST00000329125
 
ENST00000611961
 
 
 
 


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
Show all »
Show » Show » 652 71.5 Yes 1
GP1BA-201 ENSP00000484439
ENST00000611961
P07359
Show all »
Show » Show » 626 69 Yes 1