TUSC3

Gene

tumor suppressor candidate 3

HGNCHGNC:30242 EnsemblENSG00000104723 NCBI Gene7991

Locus: gene with protein productLocation: 8p22

Also known as

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

Also known asMRT22 · MGC13453 · N33 · OST3A · MRT7 · MagT2 · SLC58A2

View full nomenclature history (10)

Previous symbolsMRT22

Alias symbolsMGC13453, N33, OST3A, MRT7, MagT2, SLC58A2

Previous namesmental retardation, non-syndromic, autosomal recessive, 22

Alias namesoligosaccharyltransferase 3 homolog A (S. cerevisiae), Magnesium uptake/transporter TUSC3

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.

Autosomal recessive non-syndromic intellectual disability

Dengue

Genetic Diseases, Inborn

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.

Oligosaccharyltransferase complex subunitsSolute carrier family 58

Provenance

HGNCCanonical human gene identity from HGNC (release 2026-07-07), updated 2023-03-14.

Open TargetsGene–disease associations from the Open Targets Platform.