Click here to close Hello! We notice that you are using Internet Explorer, which is not supported by Xenbase and may cause the site to display incorrectly. We suggest using a current version of Chrome, FireFox, or Safari.

Summary Expression Phenotypes Gene Literature (6) GO Terms (13) Nucleotides (94) Proteins (53) Interactants (67) Wiki
XB-GENEPAGE-1000031
???displayGene.symbol???:
 slc26a5

???displayGene.name???: 
solute carrier family 26 member 5

???displayGene.synonyms???
prestin ( Nomenclature history )

???displayGene.geneFunction???
anion exchanger

AI Protein Function :
The slc26a5 gene encodes prestin, a motor protein localized to the lateral membrane of outer hair cells in the basilar papilla; it functions as an anion transporter and voltage-dependent motor protein ...[+]



???displayGene.geneInteractants???
Loading ...

Diseases: 


Disease Ontology:
autosomal recessive nonsyndromic deafness [+]

MIM:
DEAFNESS, AUTOSOMAL RECESSIVE 61; DFNB61

External Links:
Loading gene data...
Please wait while we fetch the latest information
???displayGene.expression???                  Development Stages                                               Embryonic Tissues                                                                Adult Tissues
More Information
Xenbase Expression Details In situ images Single cell data at SPRING In situ: RNA-Seq:


Symbol legend: Blast sequence    View sequence    Literature or expression images   Hover cursor for info