EC Number |
BRENDA No. |
Title |
Journal |
Volume |
Pages |
Year |
Organism |
PubMed ID |
---|
2.4.1.267 | 758995 |
Novel genetic variants of ALG6 and GALNTL4 of the glycosylation pathway predict cutaneous melanoma-specific survival |
Cancers (Basel) |
12 |
288 |
2020 |
Homo sapiens |
31991610 |
2.4.1.267 | 759846 |
Structure and mechanism of the ER-based glucosyltransferase ALG6 |
Nature |
579 |
443-447 |
2020 |
Saccharomyces cerevisiae |
32103179 |
2.4.1.267 | 708652 |
A frequent mild mutation in ALG6 may exacerbate the clinical severity of patients with congenital disorder of glycosylation Ia (CDG-Ia) caused by phosphomannomutase deficiency |
Hum. Mol. Genet. |
11 |
599-604 |
2002 |
Homo sapiens |
11875054 |
2.4.1.267 | 709966 |
Analysis of multiple mutations in the hALG6 gene in a patient with congenital disorder of glycosylation Ic |
Mol. Genet. Metab. |
70 |
219-223 |
2000 |
Homo sapiens |
10924277 |
2.4.1.267 | 723575 |
Engineering Yarrowia lipolytica to produce glycoproteins homogeneously modified with the universal Man3GlcNAc2 N-glycan core |
PLoS ONE |
7 |
e39976 |
2012 |
Yarrowia lipolytica |
22768188 |
2.4.1.267 | 708659 |
Identification of a frequent variant in ALG6, the cause of congenital disorder of glycosylation-Ic |
Hum. Mutat. |
22 |
420-421 |
2003 |
Homo sapiens |
14517965 |
2.4.1.267 | 708620 |
Isolation of the ALG6 locus of Saccharomyces cerevisiae required for glucosylation in the N-linked glycosylation pathway |
Glycobiology |
6 |
493-498 |
1996 |
Saccharomyces cerevisiae |
8877369 |
2.4.1.267 | 736204 |
Reduced expression of the oligosaccharyltransferase exacerbates protein hypoglycosylation in cells lacking the fully assembled oligosaccharide donor |
Glycobiology |
25 |
774-783 |
2015 |
Cricetulus griseus |
25792706 |
2.4.1.267 | 736204 |
Reduced expression of the oligosaccharyltransferase exacerbates protein hypoglycosylation in cells lacking the fully assembled oligosaccharide donor |
Glycobiology |
25 |
774-783 |
2015 |
Homo sapiens |
25792706 |
2.4.1.267 | 708197 |
Skeletal dysplasia with brachytelephalangy in a patient with a congenital disorder of glycosylation due to ALG6 gene mutations |
Clin. Genet. |
77 |
507-509 |
2010 |
Homo sapiens |
20447155 |