Biology:Zinc finger protein 592

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Short description: Protein found in humans


A representation of the 3D structure of the protein myoglobin showing turquoise α-helices.
Generic protein structure example


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

  1. ↑ "Entrez Gene: Zinc finger protein 592". https://www.ncbi.nlm.nih.gov/gene/9640. 

Further reading

This article incorporates text from the United States National Library of Medicine, which is in the public domain.




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