solute carrier family 24 member 1

Summary
Gene Symbol
  • SLC24A1
Organism
Homo sapiens (human)
NCBI Gene
9187
PubChem
9187
Alliance of Genome Resources
Annotation
Keyword
  • Alternative splicing
  • Antiport
  • Calcium transport
  • Cell membrane
  • Congenital stationary night blindness
  • Glycoprotein
  • Phosphoprotein
  • Proteomics identification
  • Reference proteome
  • Repeat
  • Sensory transduction
  • Signal
  • Symport
  • Transmembrane helix
  • Vision
Proteins
Displaying all 4 entries
UniProt Protein Name
B4DUG1
  • Na(+)/K(+)/Ca(2+)-exchange protein 1
  • Retinal rod Na-Ca+K exchanger
  • Solute carrier family 24 member 1
B4E1W0
  • Na(+)/K(+)/Ca(2+)-exchange protein 1
  • Retinal rod Na-Ca+K exchanger
  • Solute carrier family 24 member 1
F5H127
  • Na(+)/K(+)/Ca(2+)-exchange protein 1
  • Retinal rod Na-Ca+K exchanger
  • Solute carrier family 24 member 1
O60721
  • Na(+)/K(+)/Ca(2+)-exchange protein 1
  • Retinal rod Na-Ca+K exchanger
  • Solute carrier family 24 member 1
Gene Ontology (GO)
GO Hierarchy
GO Hierarchy
OrthoDB (Group)
Group level
Eukaryota
Group Name
sodium/potassium/calcium exchanger
Functional Category
  • E: Amino acid transport and metabolism
  • P: Inorganic ion transport and metabolism
  • T: Signal transduction mechanisms
Disease
Disease Ontology
Displaying 1 entry
DO ID Disease Name Source
DOID:0110868 congenital stationary night blindness 1D

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Acknowledgements

Supported by JST NBDC Grant Number JPMJND2204

Partly supported by NIH Common Fund Grant #1U01GM125267-01


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Last updated: December 9, 2024