Zinc finger protein 592
Zinc finger protein 592 is a protein that in humans is encoded by the ZNF592 gene. [1]
Function
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.
References
- ↑ “Entrez Gene: Zinc finger protein 592”. Retrieved 2016-03-07.
Further reading
- Huang J, Zheng DL, Qin FS, Cheng N, Chen H, Wan BB, Wang YP, Xiao HS, Han ZG (2010). “Genetic and epigenetic silencing of SCARA5 may contribute to human hepatocellular carcinoma by activating FAK signaling”. J. Clin. Invest. 120 (1): 223–41. doi:10.1172/JCI38012. PMC 2798676. PMID 20038795.
This article incorporates text from the United States National Library of Medicine, which is in the public domain.
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