CLDN14

GENERAL INFORMATION

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Gene name

CLDN14

Gene description

Claudin 14

Protein class

Disease related genes
Predicted membrane proteins

Predicted localization

Membrane

Number of transcripts

5
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HUMAN PROTEIN ATLAS INFORMATION

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RNA tissue category

HPA:Group enriched (kidney, liver)
GTEx:Group enriched (kidney, liver)

Protein evidence

Evidence at protein level

ANTIBODY RELIABILITY

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Data reliability

Pending normal tissue annotation.
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RNA AND PROTEIN EXPRESSION SUMMARY

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RNA expression (FPKM) Protein expression (score)
Brain
N/A
Endocrine tissues
N/A
Bone marrow & immune system
N/A
Muscle tissues
N/A
Lung
N/A
Nasopharynx
N/A
N/A
Bronchus
N/A
N/A
Lung
N/A
Liver & gallbladder
N/A
Liver
N/A
Pancreas
N/A
Pancreas
N/A
Gastrointestinal tract
N/A
Kidney & urinary bladder
N/A
Male tissues
N/A
Testis
N/A
Epididymis
N/A
N/A
Prostate
N/A
Seminal vesicle
N/A
N/A
Female tissues
N/A
Breast
N/A
N/A
Vagina
N/A
N/A
Cervix, uterine
N/A
N/A
Ovary
N/A
Placenta
N/A
Adipose & soft tissue
N/A
Skin
N/A
Skin
N/A


PROTEIN EXPRESSION OVERVIEW

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Pending normal tissue annotation.


RNA EXPRESSION OVERVIEW

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HPA dataset
RNA tissue category:  Group enriched (kidney, liver)

Organ

Expression

GTEx dataset
RNA tissue category:  Group enriched (kidney, liver)

Organ

Expression



GENE INFORMATION

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Gene name

CLDN14 (HGNC Symbol)

Synonyms

DFNB29

Description

Claudin 14 (HGNC Symbol)

Entrez gene summary

Tight junctions represent one mode of cell-to-cell adhesion in epithelial or endothelial cell sheets, forming continuous seals around cells and serving as a physical barrier to prevent solutes and water from passing freely through the paracellular space. These junctions are comprised of sets of continuous networking strands in the outwardly facing cytoplasmic leaflet, with complementary grooves in the inwardly facing extracytoplasmic leaflet. The protein encoded by this gene, a member of the claudin family, is an integral membrane protein and a component of tight junction strands. The encoded protein also binds specifically to the WW domain of Yes-associated protein. Defects in this gene are the cause of an autosomal recessive form of nonsyndromic sensorineural deafness. It is also reported that four synonymous variants in this gene are associated with kidney stones and reduced bone mineral density. Several transcript variants encoding the same protein have been found for this gene. [provided by RefSeq, Jun 2010]

Chromosome

21

Cytoband

q22.13

Chromosome location (bp)

36460621 - 36576569

Protein evidence

Evidence at protein level (all genes)

Ensembl

ENSG00000159261 (version 78.38)

Entrez gene

23562

UniProt

O95500 (UniProt - Evidence at protein level)

neXtProt

NX_O95500

Antibodypedia

CLDN14 antibodies


PROTEIN BROWSER

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ENST00000342108
 
ENST00000399135
 
ENST00000399136
 
ENST00000399137
 
ENST00000399139
 
 
 
 


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)

CLDN14-001 ENSP00000382090
ENST00000399137
O95500
Show all »
Show » Show » 239 25.7 No 3
CLDN14-002 ENSP00000382087
ENST00000399135
O95500
Show all »
Show » Show » 239 25.7 No 3
CLDN14-003 ENSP00000382088
ENST00000399136
O95500
Show all »
Show » Show » 239 25.7 No 3
CLDN14-004 ENSP00000339292
ENST00000342108
O95500
Show all »
Show » Show » 239 25.7 No 3
CLDN14-006 ENSP00000382092
ENST00000399139
O95500
Show all »
Show » Show » 239 25.7 No 3