Slc24a1 - solute carrier family 24 member 1 Gene

Also Known as Nckx1

Species: Rattus norvegicus

Gene Type: protein coding
Gene ID: 56814

Summary

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]

Slc24a1 Products (1)

mRNA Protein Name
NM_020090.1 NP_064475.1 sodium/potassium/calcium exchanger 1

Gene Ontology

  • Biological Process
  • Cellular Component
Biological Process GO Annotation Evidence References Source
involved in calcium ion transmembrane transport IDA
IDA: Inferred from direct assay
10751314 RGD
Cellular Component GO Annotation Evidence References Source
located in cell surface IDA
IDA: Inferred from direct assay
10751314 RGD
EXP: Inferred from Experiment IDA: Inferred from direct assay IPI: Inferred from physical interaction IMP: Inferred from mutant phenotype IGI: Inferred from genetic interaction IEP: Inferred from expression pattern
Protein Preferred Names Protein Names

sodium/potassium/calcium exchanger 1

  • Na(+)/K(+)/Ca(2+)-exchange protein 1

  • retinal Na/Ca,K exchanger

  • retinal rod Na-Ca+K exchanger

  • sodium/calcium/potassium exchanger

  • solute carrier family 24 (sodium/potassium/calcium exchanger), 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