Zinc finger protein 592: Difference between revisions

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==Function==
==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.
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 ==
== References ==

Latest revision as of 12:48, 9 January 2019

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Identifiers
Aliases
External IDsGeneCards: [1]
Orthologs
SpeciesHumanMouse
Entrez

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Ensembl

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UniProt

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RefSeq (mRNA)

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RefSeq (protein)

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Location (UCSC)n/an/a
PubMed searchn/an/a
Wikidata
View/Edit Human

Zinc finger protein 592 is a protein that in humans is encoded by the ZNF592 gene. [1]

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. ↑ "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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