Homo sapiens Protein: CLDN14
Summary
InnateDB Protein IDBP-231418.5
Last Modified 2014-10-13 [Report errors or provide feedback]
Gene Symbol CLDN14
Protein Name claudin 14
Synonyms DFNB29;
Species Homo sapiens
Ensembl Protein ENSP00000382090
InnateDB Gene IDBG-2998 (CLDN14)
Protein Structure
UniProt Annotation
Function Plays a major role in tight junction-specific obliteration of the intercellular space, through calcium- independent cell-adhesion activity. {ECO:0000250}.
Subcellular Localization Cell junction, tight junction. Cell membrane; Multi-pass membrane protein.
Disease Associations Deafness, autosomal recessive, 29 (DFNB29) [MIM:614035]: A form of non-syndromic sensorineural hearing loss. Sensorineural deafness results from damage to the neural receptors of the inner ear, the nerve pathways to the brain, or the area of the brain that receives sound information. {ECO:0000269PubMed:11163249, ECO:0000269PubMed:22246673, ECO:0000269PubMed:23235333}. Note=The disease is caused by mutations affecting the gene represented in this entry.
Tissue Specificity Liver, kidney. Also found in ear.
Comments
Interactions
Number of Interactions This gene and/or its encoded proteins are associated with 0 experimentally validated interaction(s) in this database.
Gene Ontology

Molecular Function
Accession GO Term
GO:0005198 structural molecule activity
GO:0005515 protein binding
GO:0042802 identical protein binding
Biological Process
GO:0006461 protein complex assembly
GO:0016338 calcium-independent cell-cell adhesion
GO:0034329 cell junction assembly
GO:0045216 cell-cell junction organization
GO:0070830 tight junction assembly
Cellular Component
GO:0005783 endoplasmic reticulum
GO:0005886 plasma membrane
GO:0005923 tight junction
GO:0016021 integral component of membrane
Protein Structure and Domains
PDB ID
InterPro IPR004031 PMP-22/EMP/MP20/Claudin superfamily
IPR005411 Claudin-2
IPR006187 Claudin
PFAM PF00822
PF13903
PRINTS PR01589
PR01077
PIRSF
SMART
TIGRFAMs
Post-translational Modifications
Modification
Cross-References
SwissProt O95500
PhosphoSite PhosphoSite-O95500
TrEMBL
UniProt Splice Variant
Entrez Gene 23562
UniGene Hs.741857
RefSeq NP_652763
HUGO HGNC:2035
OMIM 605608
CCDS CCDS13645
HPRD 05727
IMGT
EMBL AF314090 AJ132445 AJ566765 AJ566766 AP001726 AY355348 AY355349 AY358533 BC012126
GenPept AAG60052 AAH12126 AAQ88897 AAR05858 AAR05859 BAA95509 CAA10669 CAD97762 CAD97763