{"symbol":"ZNF592","synonyms":["CAMOS","SCAR5"],"name":"zinc finger protein 592","description":"This gene is thought to play a role in a complex developmental pathway and the regulation of genes involved in cerebellar development. Mutations in this gene have been associated with autosomal recessive spinocerebellar ataxia. [provided by RefSeq, Jan 2011]","ncbiEntrezGeneId":9640,"ncbiEntrezGeneUrl":"http://www.ncbi.nlm.nih.gov/gene/9640","proteins":[{"symbol":"ZN592_HUMAN","href":"/api/1.0/protein/ZN592_HUMAN"}],"hgncRootFamilies":[{"name":"Zinc fingers","href":"/api/1.0/gene_family/Zinc+fingers"}]}