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SLC5A7

Gene

solute carrier family 5 member 7

HGNCHGNC:14025EnsemblENSG00000115665NCBI Gene60482
Locus: gene with protein productLocation: 2q12.3

Also known as

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

Also known ashCHT · CHT1 · ChT
View full nomenclature history (6)
Alias symbolshCHT, CHT1, ChT
Previous namessolute carrier family 5 (choline transporter), member 7, solute carrier family 5 (sodium/choline cotransporter), member 7
Alias namesHigh affinity choline transporter 1

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 myasthenic syndromes
Muscular Atrophy
Genetic Diseases, Inborn
Familial prostate cancer

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 5

Provenance

HGNCCanonical human gene identity from HGNC (release 2026-07-07), updated 2023-01-20.
Open TargetsGene–disease associations from the Open Targets Platform.