Zinc finger protein 592

(Redirected from ZNF592)

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; OMA:ZNF592 - orthologs
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 MbChr 7: 80.64 – 80.69 Mb
PubMed search[3][4]
Wikidata
View/Edit HumanView/Edit Mouse

Function

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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

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  1. ^ a b c GRCh38: Ensembl release 89: ENSG00000166716Ensembl, May 2017
  2. ^ a b c GRCm38: Ensembl release 89: ENSMUSG00000005621Ensembl, 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

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