| Gene Symbol | ALG14 |
| Entrez Gene ID | 199857 |
| Full Name | ALG14, UDP-N-acetylglucosaminyltransferase subunit |
| Synonyms | CMS15 |
| General protein information |
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| Gene Type | protein-coding |
| Organism | Homo sapiens(human) |
| Genome | |
| Summary | 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]. |
| Disorder MIM: | |
| Disorder Html: | ?Myasthenic syndrome, congenital, 15, without tubular aggregates, 616227 (3) |









































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