This gene is a member of the glycosyltransferase 1 family. The encoded protein and ALG13 are thought to be subunits of UDP-GlcNAc transferase, which catalyzes the first two committed steps in endoplasmic reticulum N-linked glycosylation. Mutations in this gene have been linked to congenital myasthenic syndrome (CMSWTA). Alternatively spliced transcript variants have been identified. [provided by RefSeq, Mar 2015]
| SKU | Test Kits | Buffer | Dye Color | Order Now |
|---|---|---|---|---|
| ALG14-20-RE | 20 (40 μL) | 200 μL |  |
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| ALG14-20-OR | 20 (40 μL) | 200 μL |  |
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| ALG14-20-GO | 20 (40 μL) | 200 μL |  |
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| ALG14-20-GR | 20 (40 μL) | 200 μL |  |
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| ALG14-20-AQ | 20 (40 μL) | 200 μL |  |
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This gene is a member of the glycosyltransferase 1 family. The encoded protein and ALG13 are thought to be subunits of UDP-GlcNAc transferase, which catalyzes the first two committed steps in endoplasmic reticulum N-linked glycosylation. Mutations in this gene have been linked to congenital myasthenic syndrome (CMSWTA). Alternatively spliced transcript variants have been identified. [provided by RefSeq, Mar 2015]
Gene Symbol : ALG14
Gene Name : ALG14, UDP-N-acetylglucosaminyltransferase subunit
Chromosome : CHR 1: 950,729,73-949,815,64
Locus : 1p21.3
Alt. Genes : ZNF263
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