SLC24A1

Gene

solute carrier family 24 member 1

HGNCHGNC:10975 EnsemblENSG00000074621 NCBI Gene9187

Locus: gene with protein productLocation: 15q22.31

Also known as

Symbols and names change; identity (the HGNC ID) does not. Previous and alternative forms are kept distinct.

Also known asNCKX1 · NCKX · RODX · KIAA0702 · HsT17412 · CSNB1D

View full nomenclature history (9)

Alias symbolsNCKX1, NCKX, RODX, KIAA0702, HsT17412, CSNB1D

Previous namessolute carrier family 24 (sodium/potassium/calcium exchanger), member 1

Alias namesNa/Ca-K exchanger 1, retinal rod Na+/Ca+/K+ exchanger

Associated diseases

via associated_with

Diseases linked to this gene through the canonical GENE→DISEASE (associated_with) relation, drawn from Open Targets' top-ranked associations by overall score — not the full association set. Disease-level detail lives on each disease's own page.

Congenital stationary night blindness

Retinitis Pigmentosa

Retinal Dystrophies

Neurodegenerative Diseases

Ovarian dysfunction

Genetic Diseases, Inborn

Alzheimer's Disease

Optic Atrophy

Drawn from Open Targets’ top 10 associations by overall score for this gene — the subset resolved to a canonical disease. Lower-ranked associations, and diseases not yet canonicalised, are not shown.

Gene family

HGNC gene-group membership.

Solute carrier family 24

Provenance

HGNCCanonical human gene identity from HGNC (release 2026-07-07), updated 2023-01-20.

Open TargetsGene–disease associations from the Open Targets Platform.