| Gene Symbol | CWF19L1 |
| Entrez Gene ID | 55280 |
| Full Name | CWF19 like 1, cell cycle control (S. pombe) |
| Synonyms | C19L1,SCAR17,hDrn1 |
| General protein information |
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| Gene Type | protein-coding |
| Organism | Homo sapiens(human) |
| Genome | |
| Summary | This gene encodes a member of the CWF19 protein family. Mutations in this gene have been associated with autosomal recessive spinocerebellar ataxia-17 and mild cognitive disability. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Dec 2014]. |
| Disorder MIM: | |
| Disorder Html: | Spinocerebellar ataxia, autosomal recessive 17, 616127 (3) |

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