CLDN4

GENERAL INFORMATION

? »

Gene name

CLDN4

Gene description

Claudin 4

Protein class

Cancer-related genes
Disease related genes
Potential drug targets
Predicted membrane proteins
Transporters

Predicted localization

Membrane

Number of transcripts

3
SHOW MORE

HUMAN PROTEIN ATLAS INFORMATION

? »

RNA tissue category

HPA:Mixed
GTEx:Mixed

Protein evidence

Evidence at protein level

Protein localization

Membranous expression in several tissues, most abundant in gastrointestinal tract.

ANTIBODY RELIABILITY

? »

Data reliability
description

Antibody staining mainly consistent with RNA expression data. Caution, targets protein from more than one gene. Presumed off target binding observed and disregarded.

Data reliability

Supportive based on 2 antibodies.
HPA007322 , CAB002610
SHOW MORE

RNA AND PROTEIN EXPRESSION SUMMARY

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

Lymph node

Liver

Esophagus

Colon

Kidney

Testis



PROTEIN EXPRESSION OVERVIEW

? »

Organ

Expression



RNA EXPRESSION OVERVIEW

? »
HPA dataset
RNA tissue category:  Mixed

Organ

Expression

GTEx dataset
RNA tissue category:  Mixed

Organ

Expression



GENE INFORMATION

? »

Gene name

CLDN4 (HGNC Symbol)

Synonyms

CPE-R, CPETR, CPETR1, hCPE-R, WBSCR8

Description

Claudin 4 (HGNC Symbol)

Entrez gene summary

The protein encoded by this intronless gene belongs to the claudin family. Claudins are integral membrane proteins that are components of the epithelial cell tight junctions, which regulate movement of solutes and ions through the paracellular space. This protein is a high-affinity receptor for Clostridium perfringens enterotoxin (CPE) and may play a role in internal organ development and function during pre- and postnatal life. This gene is deleted in Williams-Beuren syndrome, a neurodevelopmental disorder affecting multiple systems. [provided by RefSeq, Sep 2013]

Chromosome

7

Cytoband

q11.23

Chromosome location (bp)

73799542 - 73832693

Protein evidence

Evidence at protein level (all genes)

Ensembl

ENSG00000189143 (version 78.38)

Entrez gene

1364

UniProt

O14493 (UniProt - Evidence at protein level)

neXtProt

NX_O14493

Antibodypedia

CLDN4 antibodies


PROTEIN BROWSER

? »
 
 
 
ENST00000340958
 
ENST00000431918
 
ENST00000435050
 
 
 
 


PROTEIN INFORMATION

? »

Splice variant

Ensembl

UniProt

Protein class

Gene ontology

Length
(aa)

Molecular mass
(kDa)

Signal peptide
(predicted)

Transmembrane regions
(predicted)

CLDN4-001 ENSP00000388639
ENST00000431918
O14493
Show all »
Show » Show » 209 22.1 No 3
CLDN4-002 ENSP00000409544
ENST00000435050
O14493
Show all »
Show » Show » 209 22.1 No 3
CLDN4-201 ENSP00000342445
ENST00000340958
O14493
Show all »
Show » Show » 209 22.1 No 3