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ENRat
Slc24a1 - solute carrier family 24 member 1
Alias:
Nckx1
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Enables calcium, potassium:sodium antiporter activity. Involved in calcium ion transmembrane transport. Is intrinsic component of plasma membrane. Human ortholog(s) of this gene implicated in congenital stationary night blindness 1D. Orthologous to human SLC24A1 (solute carrier family 24 member 1). [provided by Alliance of Genome Resources, Apr 2022]
Basic Information
NCBI
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Slc24a1 Genetics information (-)
mRatBN7.2
Sequence Homology
Transcripts & Proteins
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* This data comes from NCBI.
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