Zinc finger protein 592

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.

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• {{cite journal |vauthors=Huang J, Zheng DL, Qin FS, Cheng N, Chen H, Wan BB, Wang YP, Xiao HS, Han ZG |title=Genetic and epigenetic silencing of SCARA5 may contribute to human hepatocellular carcinoma by activating FAK signaling |journal=J. Clin. Invest. |volume=120 |issue=1 |pages=223–41 |year=2010 |pmid=20038795 |pmc=2798676 |doi=10.1172/JCI38012 }}

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Category:Human proteins

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