SLC47A1

Gene

solute carrier family 47 member 1

HGNCHGNC:25588 EnsemblENSG00000142494 NCBI Gene55244

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 asFLJ10847 · MATE1

View full nomenclature history (4)

Alias symbolsFLJ10847, MATE1

Previous namessolute carrier family 47 (multidrug and toxin extrusion), member 1

Alias namesmultidrug and toxin extrusion 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.

Neurodegenerative Diseases

Intracranial Aneurysm

Diabetes Mellitus, Type 2

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.

Small nucleolar RNA protein coding host genesSolute carrier family 47

Provenance

HGNCCanonical human gene identity from HGNC (release 2026-07-07), updated 2023-01-20.

Open TargetsGene–disease associations from the Open Targets Platform.