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XB-GENEPAGE-482084
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 slc4a11

???displayGene.name???: 
solute carrier family 4 member 11

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XNBC2 ( Nomenclature history )

???displayGene.geneFunction???
transmembrane solute exchange

AI Protein Function :
slc4a11 encodes a membrane transport protein that functions as a sodium‑bicarbonate cotransporter, localizing to the basolateral plasma membrane of epithelial cells; expression is documented in the pro...[+]



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Diseases: 


Disease Ontology:
congenital hereditary endothelial dystrophy of cornea [+]

MIM:
CORNEAL ENDOTHELIAL DYSTROPHY; CHED [+]

External Links:
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???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:


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