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SLC38A11

Gene

solute carrier family 38 member 11

HGNCHGNC:26836EnsemblENSG00000169507NCBI Gene151258
Locus: gene with protein productLocation: 2q24.3

Also known as

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

Also known asFLJ39822 · AVT2
View full nomenclature history (3)
Alias symbolsFLJ39822, AVT2
Previous namessolute carrier family 38, member 11

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.

Diabetes Mellitus, Type 2
Diabetes Mellitus
Aortic Diseases
Narcolepsy
Glaucoma, Open-Angle
Wounds and Injuries
Alcohol drinking
Seasonal allergic rhinitis

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 38

Provenance

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