Difference between revisions of "YOR002W"
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| − | '''Description of YOR002W:''' | + | '''Description of YOR002W:''' Alpha 1,3 glucosyltransferase, involved in transfer of oligosaccharides from dolichyl pyrophosphate to asparagine residues of proteins during N-linked protein glycosylation; mutations in human ortholog are associated with disease<ref name='S000055554'>Reiss G, et al. (1996) Isolation of the ALG6 locus of Saccharomyces cerevisiae required for glucosylation in the N-linked glycosylation pathway. Glycobiology 6(5):493-8 {{SGDpaper|S000055554}} PMID 8877369</ref><ref name='S000039314'>Imbach T, et al. (1999) A mutation in the human ortholog of the Saccharomyces cerevisiae ALG6 gene causes carbohydrate-deficient glycoprotein syndrome type-Ic. Proc Natl Acad Sci U S A 96(12):6982-7 |
{{SGDpaper|S000039314}} PMID 10359825</ref> | {{SGDpaper|S000039314}} PMID 10359825</ref> | ||
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Revision as of 07:21, 26 February 2009
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| Systematic name | YOR002W |
| Gene name | ALG6 |
| Aliases | |
| Feature type | ORF, Verified |
| Coordinates | Chr XV:329418..331052 |
| Primary SGDID | S000005528 |
Description of YOR002W: Alpha 1,3 glucosyltransferase, involved in transfer of oligosaccharides from dolichyl pyrophosphate to asparagine residues of proteins during N-linked protein glycosylation; mutations in human ortholog are associated with disease[1][2]
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References
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- ↑ Reiss G, et al. (1996) Isolation of the ALG6 locus of Saccharomyces cerevisiae required for glucosylation in the N-linked glycosylation pathway. Glycobiology 6(5):493-8 SGD PMID 8877369
- ↑ Imbach T, et al. (1999) A mutation in the human ortholog of the Saccharomyces cerevisiae ALG6 gene causes carbohydrate-deficient glycoprotein syndrome type-Ic. Proc Natl Acad Sci U S A 96(12):6982-7 SGD PMID 10359825
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