Entity Details

Primary name CLDN14
Entity type gene
Source Source Link

Details

PrimaryID23562
RefseqGeneNG_011777
SymbolCLDN14
Nameclaudin 14
Chromosome21
Location21q22.13
TaxID9606
Statuslive
SourceGenomegenomic
SourceOriginnatural
CreationDate2000-02-20
ModificationDate2021-06-11

Ontological Relatives

UniProt IDsCLD14_HUMAN

GO terms

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GOName
GO:0005198 structural molecule activity
GO:0005783 endoplasmic reticulum
GO:0005886 plasma membrane
GO:0005923 bicellular tight junction
GO:0007155 cell adhesion
GO:0016021 integral component of membrane
GO:0016338 calcium-independent cell-cell adhesion via plasma membrane cell-adhesion molecules
GO:0042802 identical protein binding
GO:0065003 protein-containing complex assembly
GO:0070830 bicellular tight junction assembly

Diseases

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Disease IDSourceNameDescription
614035 OMIMDeafness, autosomal recessive, 29 (DFNB29)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. The disease is caused by variants affecting the gene represented in this entry.

Interactions

4 interactions

InteractorPartnerSourcesPublicationsLink
CLDN14PLEKHA1BioGRID, IntAct27107012 details
CLDN14PLLPBioGRID, IntAct32296183 details
CLDN14CTXN3BioGRID, IntAct32296183 details
CLDN14MALBioGRID, IntAct32296183 details