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SLC5A10

Gene

solute carrier family 5 member 10

HGNCHGNC:23155EnsemblENSG00000154025NCBI Gene125206
Locus: gene with protein productLocation: 17p11.2

Also known as

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

Also known asSGLT5
View full nomenclature history (3)
Alias symbolsSGLT5
Previous namessolute carrier family 5 (sodium/glucose cotransporter), member 10, solute carrier family 5 (sodium/sugar cotransporter), member 10

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.

Ovarian dysfunction
Brugada syndrome
Familial progressive cardiac conduction defect
Atrial Fibrillation
Familial isolated dilated cardiomyopathy

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.