Species Human Entrez 9640 | Human Mouse Ensembl ENSG00000166716 | |
Aliases ZNF592, CAMOS, SCAR5, zinc finger protein 592 External IDs MGI: 2443541 HomoloGene: 8759 GeneCards: ZNF592 | ||
Zinc finger protein 592 is a protein that in humans is encoded by the ZNF592 gene.
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
Zinc finger protein 592 Wikipedia(Text) CC BY-SA