ALG9

Gene

ALG9 alpha-1,2-mannosyltransferase

HGNCHGNC:15672 EnsemblENSG00000086848 NCBI Gene79796

Locus: gene with protein productLocation: 11q23.1

Also known as

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

Also known asDIBD1

View full nomenclature history (8)

Previous symbolsDIBD1

Previous namesdisrupted in bipolar affective disorder 1, asparagine-linked glycosylation 9 homolog (yeast, alpha 1,2 mannosyltransferase), asparagine-linked glycosylation 9, alpha- 1,2-mannosyltransferase homolog (S. cerevisiae, alpha- 1,2-mannosyltransferase), asparagine-linked glycosylation 9, alpha-1,2-mannosyltransferase homolog (S. cerevisiae)

Alias namesdolichyl-P-Man:Man(6)GlcNAc(2)-PP-dolichol alpha-1,2-mannosyltransferase, dolichyl-P-Man:Man(8)GlcNAc(2)-PP-dolichol alpha-1,2-mannosyltransferase, dol-P-Man dependent 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.

Polycystic Kidney, Autosomal Dominant

Neurodegenerative Diseases

Congenital disorder of glycosylation

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.

Dolichyl D-mannosyl phosphate dependent mannosyltransferases

Provenance

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

Open TargetsGene–disease associations from the Open Targets Platform.