SLC33A1

Gene

solute carrier family 33 member 1

HGNCHGNC:95 EnsemblENSG00000169359 NCBI Gene9197

Locus: gene with protein productLocation: 3q25.31

Also known as

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

Also known asACATN · SPG42 · AT-1 · AT1

View full nomenclature history (8)

Previous symbolsACATN, SPG42

Alias symbolsAT-1, AT1

Previous namesacetyl-Coenzyme A transporter, spastic paraplegia 42 (autosomal dominant), solute carrier family 33 (acetyl-CoA transporter), member 1

Alias namesAcetyl-CoA transporter 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

Spastic Paraplegia, Hereditary

Cataract

Epilepsies, Partial

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 33

Provenance

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

Open TargetsGene–disease associations from the Open Targets Platform.