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Summary Expression Phenotypes Gene Literature (0) GO Terms (22) Nucleotides (70) Proteins (34) Interactants (5) Wiki
XB-GENEPAGE-991429
???displayGene.symbol???:
 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 protein localized to the cell membrane. This transporter functions in melanocytes of the skin and retinal pigment epithelium to regulate i...[+]


InterPro :
K/Na/Ca-exchanger, NaCa Exmemb, ARM-type fold, NCX ion-bd dom sf

???displayGene.geneInteractants???
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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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