GPC3

GENERAL INFORMATION

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Gene name

GPC3

Gene description

Glypican 3

Protein class

Cancer-related genes
Disease related genes
Predicted intracellular proteins
Predicted membrane proteins

Predicted localization

Intracellular,Membrane

Number of transcripts

3
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HUMAN PROTEIN ATLAS INFORMATION

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RNA tissue category

HPA:Tissue enhanced (placenta)
GTEx:Tissue enhanced (adipose tissue, lung)

Protein evidence

Evidence at protein level

Protein localization

Ubiquitous cytoplasmic expression, often with a granular pattern.

ANTIBODY RELIABILITY

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Data reliability
description

Antibody staining mainly not consistent with RNA expression data. Pending external verification.

Data reliability

Uncertain based on 2 antibodies.
HPA006316 , CAB017784
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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

Lymph node

Liver

Colon

Kidney

Testis

Placenta



PROTEIN EXPRESSION OVERVIEW

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Organ

Expression



RNA EXPRESSION OVERVIEW

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HPA dataset
RNA tissue category:  Tissue enhanced (placenta)

Organ

Expression

GTEx dataset
RNA tissue category:  Tissue enhanced (adipose tissue, lung)

Organ

Expression



GENE INFORMATION

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Gene name

GPC3 (HGNC Symbol)

Synonyms

DGSX, OCI-5, SDYS, SGB, SGBS, SGBS1

Description

Glypican 3 (HGNC Symbol)

Entrez gene summary

Cell surface heparan sulfate proteoglycans are composed of a membrane-associated protein core substituted with a variable number of heparan sulfate chains. Members of the glypican-related integral membrane proteoglycan family (GRIPS) contain a core protein anchored to the cytoplasmic membrane via a glycosyl phosphatidylinositol linkage. These proteins may play a role in the control of cell division and growth regulation. The protein encoded by this gene can bind to and inhibit the dipeptidyl peptidase activity of CD26, and it can induce apoptosis in certain cell types. Deletion mutations in this gene are associated with Simpson-Golabi-Behmel syndrome, also known as Simpson dysmorphia syndrome. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Sep 2009]

Chromosome

X

Cytoband

q26.2

Chromosome location (bp)

133535745 - 133985895

Protein evidence

Evidence at protein level (all genes)

Ensembl

ENSG00000147257 (version 78.38)

Entrez gene

2719

UniProt

P51654 (UniProt - Evidence at protein level)

neXtProt

NX_P51654

Antibodypedia

GPC3 antibodies


PROTEIN BROWSER

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ENST00000370818
 
ENST00000394299
 
ENST00000406757
 
 
 
 


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)

GPC3-001 ENSP00000359854
ENST00000370818
P51654
Show all »
Show » Show » 580 65.6 Yes 1
GPC3-002 ENSP00000385307
ENST00000406757
Show » Show » 256 29 No 0
GPC3-201 ENSP00000377836
ENST00000394299
P51654
Show all »
Show » Show » 603 68.4 Yes 1