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
ReMap Statistics
- Datasets
- 4
- Biotypes
- 3
- Peaks
- 54,437
- Non-redundant peaks
- 50,799
TF Classification
- Super Class
- Zinc-coordinating DNA-binding domains
- Class
- C2H2 zinc finger factors
- Familly
- Factors with multiple dispersed zinc fingers
- Sub Familly
- ZNF532-like factors
Source TFClass
External IDs
- JASPAR
- Ensembl
- ENSG00000166716
- UniProt
- Q92610
- Genevisible
- Q92610
- RefSeq
- NM_014630
- Aliases
- CAMOS; KIAA0211; SCAR5
Datasets Table for ZNF592
| Target name | Target modification | Ecotype/Strain | Biotype | Biotype modification | Source | Species | Experiment | Peaks |
|---|---|---|---|---|---|---|---|---|
| ZNF592 | GM12878 | ENCODE | Homo sapiens | ENCSR173ZVL | 5,590 | |||
| ZNF592 | K-562 | ENCODE | Homo sapiens | ENCSR249BHQ | 39,515 | |||
| ZNF592 | MCF-7 | ENCODE | Homo sapiens | ENCSR028NUR | 296 | |||
| ZNF592 | MCF-7 | ENCODE | Homo sapiens | ENCSR701AQS | 9,036 | |||
| Target name | Target modification | Ecotype/Strain | Biotype | Biotype modification | Source | Species | Experiment | Peaks |