Slc24a1 - solute carrier family 24 (sodium/potassium/calcium exchanger), member 1 Gene

Mus musculus

Gene ID: 214111 | Gene type: protein coding

About Slc24a1

Summary

Predicted to enable Calcium Channel activity and calcium, potassium:sodium antiporter activity. Predicted to be involved in cellular calcium ion homeostasis; inorganic cation transmembrane transport; and regulation of synaptic plasticity. Predicted to be located in plasma membrane. Predicted to be intrinsic component of plasma membrane. Predicted to be integral component of plasma membrane. Is expressed in cerebellum; hippocampus; retina inner nuclear layer; retina nuclear layer; and retina outer nuclear layer. Used to study congenital stationary night blindness 1D. 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]

Slc24a1 Products(2)

mRNA	Protein	Name
NM_001410501.1	NP_001397430.1	sodium/potassium/calcium exchanger 1 isoform 2
NM_144813.3	NP_659062.1	sodium/potassium/calcium exchanger 1 isoform 1

Protein Preferred Names

Protein Names

sodium/potassium/calcium exchanger 1

Na(+)/K(+)/Ca(2+)-exchange protein 1	retinal rod Na-Ca+K exchanger
solute carrier family 24 member 1

Related Agents

Pre-clinical Phase

Bioactive Molecules (1)

Cat. No.	Product Name	Effect	Purity	Rare Diseases
HY-RS13084	SLC24A1 Human Pre-designed siRNA Set A	Pre-designed Set	/	Unkown

Orthologs Information

Species	Symbol	Source	ID
Homo sapiens	Slc24a1	NCBI	NCBI:9187

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