Zinc finger protein 592

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. GRCh38: Ensembl release 89: ENSG00000166716 - Ensembl, May 2017
  2. GRCm38: Ensembl release 89: ENSMUSG00000005621 - Ensembl, May 2017
  3. "Human PubMed Reference:". National Center for Biotechnology Information, U.S. National Library of Medicine.
  4. "Mouse PubMed Reference:". National Center for Biotechnology Information, U.S. National Library of Medicine.
  5. "Entrez Gene: Zinc finger protein 592". Retrieved 2016-03-07.

Further reading

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


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