SLC38A7

Gene

solute carrier family 38 member 7

HGNCHGNC:25582 EnsemblENSG00000103042 NCBI Gene55238

Locus: gene with protein productLocation: 16q21

Also known as

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

Also known asFLJ10815 · SNAT7

View full nomenclature history (4)

Alias symbolsFLJ10815, SNAT7

Previous namessolute carrier family 38, member 7

Alias namesSodium-coupled neutral amino acid transporter 7

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.

Sleep Initiation and Maintenance Disorders

Malignant epithelial tumor of ovary

Neoplasms

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.