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 belonging to the solute carrier family 24 and functions as a plasma‑membrane transporter that extrudes Ca2+ in exchange for Na+ and K+, th...[+]
???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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