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ALG13

Gene

ALG13 UDP-N-acetylglucosaminyltransferase subunit

HGNCHGNC:30881EnsemblENSG00000101901NCBI Gene79868
Locus: gene with protein productLocation: Xq23

Also known as

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

Also known asGLT28D1 · CXorf45 · MDS031 · YGL047W · FLJ23018 · TDRD13 · CDG1S
View full nomenclature history (12)
Previous symbolsGLT28D1, CXorf45
Alias symbolsMDS031, YGL047W, FLJ23018, TDRD13, CDG1S
Previous namesglycosyltransferase 28 domain containing 1, chromosome X open reading frame 45, asparagine-linked glycosylation 13 homolog (S. cerevisiae)
Alias namestudor domain containing 13, N-acetylglucosaminyldiphosphodolichol N-acetylglucosaminyltransferase

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.

Congenital disorder of glycosylation
Genetic Diseases, Inborn
Genetic developmental and epileptic encephalopathy

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.

UDP-N-acetylglucosaminyltransferase subunitsOTU domain containingTudor domain containing

Provenance

HGNCCanonical human gene identity from HGNC (release 2026-07-07), updated 2023-03-15.
Open TargetsGene–disease associations from the Open Targets Platform.