{"symbol":"CWF19L1","synonyms":["hDrn1","C19L1","SCAR17"],"name":"CWF19-like 1, cell cycle control (S. pombe)","description":"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]","ncbiEntrezGeneId":55280,"ncbiEntrezGeneUrl":"http://www.ncbi.nlm.nih.gov/gene/55280","proteins":[{"symbol":"C19L1_HUMAN","href":"/api/1.0/protein/C19L1_HUMAN"}],"hgncRootFamilies":[]}