Species: Hu, Mu
Applications: ICC/IF, IHC
Host: Rabbit Polyclonal
Species: Hu
Applications: WB
Host: Rabbit Polyclonal
Species: Hu
Applications: AC
Description
The ALG9 gene encodes an alpha-1,2-mannosyltransferase enzyme that functions in lipid-linked oligosaccharide assembly. Mutations in this gene result in congenital disorder of glycosylation type Il. Multiple transcript variants encoding different isoforms have
Bioinformatics
Entrez |
Human |
Product By Gene ID |
79796 |
Alternate Names |
- alpha-1,2-mannosyltransferase ALG9
- asparagine-linked glycosylation 9 homolog (S. cerevisiae, alpha-1,2-mannosyltransferase)
- asparagine-linked glycosylation 9 homolog (yeast, alpha 1,2mannosyltransferase)
- 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)
- Asparagine-linked glycosylation protein 9 homolog
- CDG1L
- DIBD1FLJ21845
- disrupted in bipolar affective disorder 1
- Disrupted in bipolar disorder protein 1
- DKFZp586M2420
- EC 2.4.1.-
- LOH11CR1J
- loss of heterozygosity, 11, chromosomal region 1 gene J product
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