Zinc finger protein 592

Zinc finger protein 592 is a protein that in humans is encoded by the ZNF592 gene. [5]

ZNF592
Identifiers
AliasesZNF592, CAMOS, SCAR5, zinc finger protein 592
External IDsOMIM: 613624 MGI: 2443541 HomoloGene: 8759 GeneCards: ZNF592
Gene location (Human)
Chr.Chromosome 15 (human)[1]
Band15q25.3Start84,748,592 bp[1]
End84,806,445 bp[1]
Orthologs
SpeciesHumanMouse
Entrez

9640

233410

Ensembl

ENSG00000166716

ENSMUSG00000005621

UniProt

Q92610

Q8BHZ4

RefSeq (mRNA)

NM_014630

NM_178707

RefSeq (protein)

NP_055445

NP_848822

Location (UCSC)Chr 15: 84.75 – 84.81 MbChr 7: 80.99 – 81.05 Mb
PubMed search[3][4]
Wikidata
View/Edit HumanView/Edit Mouse

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.

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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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