Search for a gene
ALG9 - ALG9 alpha-1,2-mannosyltransferase
- Synonym(s) : dolichyl-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
- Previous symbols and names : DIBD1, 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), disrupted in bipolar affective disorder 1
- Type : gene with protein product
- Chromosomal location : 11q23.1
- OMIM: 606941
- HGNC: 15672
- UniProtKB: Q9H6U8
- Genatlas: ALG9
- GenCC: ALG9
- Ensembl: ENSG00000086848
- IUPHAR-DB: -
- Reactome: Q9H6U8
- LOVD: ALG9
Diseases list
- Disease-causing germline mutation(s) (loss of function) in ALG9-CDG
ORPHA:79328 
- Disease-causing germline mutation(s) (loss of function) in Autosomal dominant polycystic kidney disease
ORPHA:730
: AssessedAdditional information
Patient-centred resources for this gene
Research activities on this gene
Specialised Social Services
The documents contained in this web site are presented for information purposes only. The material is in no way intended to replace professional medical care by a qualified specialist and should not be used as a basis for diagnosis or treatment.
Orphanet is part of the Gene Curation Coalition, a global effort to harmonise gene-level resources.