YNL219C
(Redirected from ALG9)
Share your knowledge...Edit this entry! <protect>
| Systematic name | YNL219C |
| Gene name | ALG9 |
| Aliases | |
| Feature type | ORF, Verified |
| Coordinates | Chr XIV:237663..235996 |
| Primary SGDID | S000005163 |
Description of YNL219C: Mannosyltransferase, involved in N-linked glycosylation; catalyzes both the transfer of seventh mannose residue on B-arm and ninth mannose residue on the C-arm from Dol-P-Man to lipid-linked oligosaccharides; mutation of the human ortholog causes type 1 congenital disorders of glycosylation[1][2][3]
</protect>
Contents
Community Commentary
About Community Commentary. Please share your knowledge!
<protect>
References
See Help:References on how to add references
- ↑ Burda P, et al. (1996) Stepwise assembly of the lipid-linked oligosaccharide in the endoplasmic reticulum of Saccharomyces cerevisiae: identification of the ALG9 gene encoding a putative mannosyl transferase. Proc Natl Acad Sci U S A 93(14):7160-5 SGD PMID 8692962
- ↑ Frank CG and Aebi M (2005) ALG9 mannosyltransferase is involved in two different steps of lipid-linked oligosaccharide biosynthesis. Glycobiology 15(11):1156-63 SGD PMID 15987956
- ↑ Frank CG, et al. (2004) Identification and functional analysis of a defect in the human ALG9 gene: definition of congenital disorder of glycosylation type IL. Am J Hum Genet 75(1):146-50 SGD PMID 15148656
See Help:Categories on how to add the wiki page for this gene to a Category </protect>
