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SLC13A5

Gene

solute carrier family 13 member 5

HGNCHGNC:23089EnsemblENSG00000141485NCBI Gene284111
Locus: gene with protein productLocation: 17p13.1

Also known as

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

Also known asNACT · INDY · mINDY
View full nomenclature history (6)
Alias symbolsNACT, INDY, mINDY
Previous namessolute carrier family 13 (sodium-dependent citrate transporter), member 5
Alias namesNa(+)/citrate cotransporter, mammalian INDY homolog (Drosophila)

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.

Undetermined early-onset epileptic encephalopathy
Genetic Diseases, Inborn
Genetic developmental and epileptic encephalopathy
Alcohol drinking
Sleep Initiation and Maintenance Disorders

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 13

Provenance

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