Zinc finger protein 592

Last updated
ZNF592
Identifiers
Aliases ZNF592 , CAMOS, SCAR5, zinc finger protein 592
External IDs OMIM: 613624 MGI: 2443541 HomoloGene: 8759 GeneCards: ZNF592
Orthologs
SpeciesHumanMouse
Entrez
Ensembl
UniProt
RefSeq (mRNA)

NM_014630

NM_178707

RefSeq (protein)

NP_055445

NP_848822

Location (UCSC) Chr 15: 84.75 – 84.81 Mb Chr 7: 80.64 – 80.69 Mb
PubMed search [3] [4]
Wikidata
View/Edit Human View/Edit Mouse

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

Contents

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. 1 2 3 GRCh38: Ensembl release 89: ENSG00000166716 - Ensembl, May 2017
  2. 1 2 3 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.