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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].
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Protein Aliases: Zinc finger protein 592
Gene Aliases: CAMOS; KIAA0211; SCAR5; ZNF592
UniProt ID: (Human) Q92610
Entrez Gene ID: (Human) 9640