Gene Symbol | CWF19L1 |
Entrez Gene ID | 55280 |
Full Name | CWF19 like 1, cell cycle control (S. pombe) |
Synonyms | C19L1,SCAR17,hDrn1 |
General protein information |
|
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) |