ZNF592( Human )

Entrez Gene 9640 Entrez Gene 9640
zinc finger protein 592

Alias

CAMOS|SCAR5

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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