ALG9 Back

asparagine-linked glycosylation 9 homolog (S. cerevisiae, alpha- 1,2-mannosyltransferase)

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NCBI Description of ALG9
This 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 been found for this gene.

Community Annotation of ALG9 Add / Edit ALG9: Annotations

No community annotations yet for ALG9.
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Figure notes


• "Mouse over" a mutation to see details.
• Missense green saturation indicates evolutionary conservation of the mutated positions.
• Red hashes in protein strip are splice sites.
• Blue-white-red bars are log2 copy ratio distributions (–1 to +1) from Zack et al. (2013).


Legend

ALG9 is highly significantly mutated in
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ALG9 is significantly mutated in
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ALG9 is near significance in
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Click on a tumor type to see its full list of significant genes.

Data details


• Mutation list for ALG9