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XB-GENEPAGE-991429
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 slc24a1

???displayGene.name???: 
solute carrier family 24 member 1

???displayGene.synonyms???
LOC108711497 , LOC108712804 ( Nomenclature history )

???displayGene.geneFunction???
K+-dependent Ca2+/Na+ exchanger NCKX1 and related proteins

AI Protein Function :
slc24a1 encodes a potassium‑dependent sodium/calcium exchanger belonging to the solute carrier family 24 and functions as a plasma‑membrane transporter that extrudes Ca2+ in exchange for Na+ and K+, th...[+]



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Diseases: 


Disease Ontology:
congenital stationary night blindness [+]

MIM:
NIGHT BLINDNESS, CONGENITAL STATIONARY, TYPE 1D; CSNB1D

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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