ZNF592

Information ZNF592

Description

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]

Full Name

zinc finger protein 592

Source NCBI

Species

Homo sapiens [tax_id: 9606]

Genome

hg38

ReMap Statistics

Datasets
4
Biotypes
3
Peaks
52,073
Non-redundant peaks
48,680

TF Classification

Super Class
NA
Class
NA
Familly
NA
Sub Familly
NA

Source TFClass

External IDs

NCBI Gene
9640
Official Gene Name
ZNF592
JASPAR
Ensembl
ENSG00000166716
UniProt
Q92610
Genevisible
Q92610
RefSeq
NM_014630
Aliases
CAMOS; KIAA0211; SCAR5

External links
All peaks ZNF592
Download BED file
Non redundant peaks ZNF592
Download BED file
SEQUENCES ZNF592
Download FASTA file
DOWNLOAD All ReMap
Got to catalogue

Datasets Table for ZNF592

Target name Target modification Ecotype/Strain Biotype Biotype modification Source Species Experiment Peaks
ZNF592 MCF-7 ENCODE Homo sapiens ENCSR028NUR 295
ZNF592 MCF-7 ENCODE Homo sapiens ENCSR701AQS 8,932
ZNF592 K-562 ENCODE Homo sapiens ENCSR249BHQ 37,272
ZNF592 GM12878 ENCODE Homo sapiens ENCSR173ZVL 5,574
Target name Target modification Ecotype/Strain Biotype Biotype modification Source Species Experiment Peaks