[5] 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.

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

This article on a gene on human chromosome 15 is a stub.

You can help Wikipedia by expanding it.This protein-related article is a stub.