CLDN11

GENERAL INFORMATION

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Gene name

CLDN11

Gene description

Claudin 11

Protein class

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 (testis)
GTEx:Tissue enhanced (ovary, testis)

Protein evidence

Evidence at protein level

Protein localization

Membranous expression in sertoli cells in testis and oligodendrocytes in the CNS.

ANTIBODY RELIABILITY

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Data reliability
description

Antibody staining consistent with RNA expression data.

Data reliability

Supportive based on 2 antibodies.
HPA013166 , CAB009789
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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

Hippocampus

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 (testis)

Organ

Expression

GTEx dataset
RNA tissue category:  Tissue enhanced (ovary, testis)

Organ

Expression



GENE INFORMATION

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Gene name

CLDN11 (HGNC Symbol)

Synonyms

OSP, OTM

Description

Claudin 11 (HGNC Symbol)

Entrez gene summary

This gene encodes a member of the claudin family. Claudins are integral membrane proteins and components of tight junction strands. Tight junction strands serve as a physical barrier to prevent solutes and water from passing freely through the paracellular space between epithelial or endothelial cell sheets, and also play critical roles in maintaining cell polarity and signal transductions. The protein encoded by this gene is a major component of central nervous system (CNS) myelin and plays an important role in regulating proliferation and migration of oligodendrocytes. Mouse studies showed that the gene deficiency results in deafness and loss of the Sertoli cell epithelial phenotype in the testis. This protein is a tight junction protein at the human blood-testis barrier (BTB), and the BTB disruption is related to a dysfunction of this gene. Alternatively spliced transcript variants encoding different isoforms have been identified.[provided by RefSeq, Aug 2010]

Chromosome

3

Cytoband

q26.2

Chromosome location (bp)

170418865 - 170860380

Protein evidence

Evidence at protein level (all genes)

Ensembl

ENSG00000013297 (version 78.38)

Entrez gene

5010

UniProt

O75508 (UniProt - Evidence at protein level)

neXtProt

NX_O75508

Antibodypedia

CLDN11 antibodies


PROTEIN BROWSER

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ENST00000064724
 
ENST00000486975
 
 
 
 


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)

CLDN11-001 ENSP00000064724
ENST00000064724
O75508
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Show » Show » 207 22 No 4
CLDN11-002 ENSP00000417434
ENST00000486975
B4DFI2
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Show » Show » 165 18 No 3