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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???
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Diseases:
Disease Ontology:
autosomal recessive nonsyndromic deafness
MIM:
DEAFNESS, AUTOSOMAL RECESSIVE 61; DFNB61
External Links:
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