| Gene Symbol | RXYLT1 |
| Entrez Gene ID | 10329 |
| Full Name | ribitol xylosyltransferase 1 |
| Synonyms | HP10481,MDDGA10,TMEM5 |
| General protein information |
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| Gene Type | protein-coding |
| Organism | Homo sapiens(human) |
| Genome | |
| Summary | This gene encodes a type II transmembrane protein that is thought to have glycosyltransferase function. Mutations in this gene result in cobblestone lissencephaly. Alternative splicing results in multiple transcript variants encoding different isoforms. [provided by RefSeq, May 2013]. |
| Disorder MIM: | |
| Disorder Html: | Muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies), type A, 10, 615041 (3) |









































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