SLC3A1

Gene

solute carrier family 3 member 1

HGNCHGNC:11025 EnsemblENSG00000138079 NCBI Gene6519

Locus: gene with protein productLocation: 2p21

Also known as

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

Also known asNBAT · CSNU1 · D2H · RBAT · ATR1

View full nomenclature history (9)

Alias symbolsNBAT, CSNU1, D2H, RBAT, ATR1

Previous namessolute carrier family 3 (cystine, dibasic and neutral amino acid transporters, activator of cystine, dibasic and neutral amino acid transport), member 1, solute carrier family 3 (amino acid transporter heavy chain), member 1

Alias namesneutral and basic amino acid transport protein rBAT, amino acid 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.

Genetic Diseases, Inborn

Kidney Diseases

Autism Spectrum Disorder

Celiac Disease

Heart Arrest

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 3

Provenance

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

Open TargetsGene–disease associations from the Open Targets Platform.