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

Species: Mus musculus

Gene Type: protein coding
Gene ID: 214111

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

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