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ALG11

Gene

ALG11 alpha-1,2-mannosyltransferase

HGNCHGNC:32456EnsemblENSG00000253710NCBI Gene440138
Locus: gene with protein productLocation: 13q14.3

Also known as

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

Also known asKIAA0266 · CDG1P
View full nomenclature history (5)
Alias symbolsKIAA0266, CDG1P
Previous namesasparagine-linked glycosylation 11 homolog (S. cerevisiae, alpha-1,2-mannosyltransferase), asparagine-linked glycosylation 11, alpha-1,2-mannosyltransferase homolog (yeast)
Alias namesGDP-Man:Man(3)GlcNAc(2)-PP-dolichol alpha-1,2-mannosyltransferase

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
Neurodegenerative Diseases
Genetic Diseases, Inborn
Hepatolenticular Degeneration
Retinitis Pigmentosa

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.

Glycosyl transferases group 1 domain containing

Provenance

HGNCCanonical human gene identity from HGNC (release 2026-07-07), updated 2023-01-20.
Open TargetsGene–disease associations from the Open Targets Platform.