Zinc finger protein 592
Appearance
(Redirected from ZNF592)
ZNF592 | |||||||||||||||||||||||||||||||||||||||||||||||||||
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Aliases | ZNF592, CAMOS, SCAR5, zinc finger protein 592 | ||||||||||||||||||||||||||||||||||||||||||||||||||
External IDs | OMIM: 613624; MGI: 2443541; HomoloGene: 8759; GeneCards: ZNF592; OMA:ZNF592 - orthologs | ||||||||||||||||||||||||||||||||||||||||||||||||||
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Zinc finger protein 592 is a protein that in humans is encoded by the ZNF592 gene. [5]
Function
[edit]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
[edit]- ^ a b c GRCh38: Ensembl release 89: ENSG00000166716 – Ensembl, May 2017
- ^ a b c GRCm38: Ensembl release 89: ENSMUSG00000005621 – Ensembl, May 2017
- ^ "Human PubMed Reference:". National Center for Biotechnology Information, U.S. National Library of Medicine.
- ^ "Mouse PubMed Reference:". National Center for Biotechnology Information, U.S. National Library of Medicine.
- ^ "Entrez Gene: Zinc finger protein 592". Retrieved 2016-03-07.
Further reading
[edit]- Huang J, Zheng DL, Qin FS, Cheng N, Chen H, Wan BB, Wang YP, Xiao HS, Han ZG (2010). "Genetic and epigenetic silencing of SCARA5 may contribute to human hepatocellular carcinoma by activating FAK signaling". J. Clin. Invest. 120 (1): 223–41. doi:10.1172/JCI38012. PMC 2798676. PMID 20038795.
This article incorporates text from the United States National Library of Medicine, which is in the public domain.