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GENE INFORMATION

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Gene name

ZNF592 (HGNC Symbol)

Synonyms

CAMOS, KIAA0211, SCAR5

Description

zinc finger protein 592 (HGNC Symbol)

Entrez gene summary

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. [provided by RefSeq, Jan 2011]

Chromosome

15 (Chromosome progress)

Cytoband

q25.3

Chromosome location (bp)

85291866 - 85349659

Ensembl

ENSG00000166716 (version 69.37)

Entrez gene

9640

UniProt

Q92610

neXtProt

NX_Q92610

Antibodypedia

ZNF592 antibodies
 

PROTEIN VIEW

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ZNF592-001
 
ZNF592-003
 
ZNF592-201
 
 
 
 
 

PROTEIN INFORMATION

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Splice variant

Ensembl

UniProt

Protein class

Gene ontology

Length
(aa)

Molecular mass
(kDa)

Signal peptide
(predicted)

Transmembrane regions
(predicted)

ZNF592-001 ENSP00000452877
ENST00000560079
Q92610
Show all »
Show » Show » 1267 137.5 No 0
ZNF592-003 ENSP00000453491
ENST00000559607
H0YM74
Show all »
Show » 858 92 No 0
ZNF592-201 ENSP00000299927
ENST00000299927
Q92610
Show all »
Show » Show » 1267 137.5 No 0