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MAGT1

Gene

magnesium transporter 1

HGNCHGNC:28880EnsemblENSG00000102158NCBI Gene84061
Locus: gene with protein productLocation: Xq21.1

Also known as

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

Also known asDKFZp564K142 · IAP · OST3B · MRX95 · SLC58A1
View full nomenclature history (6)
Alias symbolsDKFZp564K142, IAP, OST3B, MRX95, SLC58A1
Alias namesoligosaccharyltransferase 3 homolog B (S. cerevisiae)

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.

Dengue
Severe Combined Immunodeficiency
Congenital disorder of glycosylation
COVID-19
Genetic Diseases, Inborn
Developmental Disabilities

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.