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 (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

Protein Function :


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

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

Diseases: 


Disease Ontology:
congenital stationary night blindness 1D [+]

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

External Links:
 
???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