CWF19L1( Human )
CWF19 like 1, cell cycle control (S. pombe)
Alias
C19L1|SCAR17|hDrn1
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 mental retardation. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Dec 2014].