Zinc finger protein 592

ZNF592
Identifiers
Aliases	ZNF592, CAMOS, SCAR5, zinc finger protein 592
External IDs	OMIM: 613624 MGI: 2443541 HomoloGene: 8759 GeneCards: ZNF592
Gene location (Human)
Chr.	Chromosome 15 (human)[1]
End	84,806,445 bp[1]
Gene location (Mouse)
Chr.	Chromosome 7 (mouse)[2]
End	81,045,164 bp[2]
Gene ontology
Molecular function	• DNA binding; • GO:0001948 protein binding; • metal ion binding; • nucleic acid binding; • GO:0001200, GO:0001133, GO:0001201 DNA-binding transcription factor activity, RNA polymerase II-specific;
Cellular component	• cell nucleus;
Biological process	• regulation of transcription, DNA-templated; • transcription, DNA-templated; • regulation of transcription from RNA polymerase II promoter;
	Sources:Amigo / QuickGO
Orthologs
	9640
	233410
	ENSG00000166716
	ENSMUSG00000005621
	Q92610
	Q8BHZ4
	NM_014630
	NM_178707
	NP_055445
	NP_848822
	Wikidata
View/Edit Human	View/Edit Mouse

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

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

GRCh38: Ensembl release 89: ENSG00000166716 - Ensembl, May 2017
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.

Zinc finger protein 592

Function

References

Further reading