ZNF513
Information ZNF513
- Description
The protein encoded by this gene is a possible transcriptional regulator involved in retinal development. Defects in this gene can be a cause of autosomal-recessive retinitis pigmentosa. Two transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Mar 2011]
- Full Name
zinc finger protein 513
Source NCBI
- Species
Homo sapiens [tax_id: 9606]
- Genome
hg38
ReMap Statistics
- Datasets
- 1
- Biotypes
- 1
- Peaks
- 12,463
- Non-redundant peaks
- 12,463
TF Classification
- Super Class
- NA
- Class
- NA
- Familly
- NA
- Sub Familly
- NA
Source TFClass
External IDs
- NCBI Gene
- 130557
- Official Gene Name
- ZNF513
- JASPAR
- Ensembl
- ENSG00000163795
- UniProt
- Q8N8E2
- Genevisible
- Q8N8E2
- RefSeq
- NM_001201459
- Aliases
- FLJ32203
Datasets Table for ZNF513
| Target name | Target modification | Ecotype/Strain | Biotype | Biotype modification | Source | Species | Experiment | Peaks |
|---|---|---|---|---|---|---|---|---|
| ZNF513 | HEK293 | ENCODE | Homo sapiens | ENCSR503DPC | 12,463 | |||
| Target name | Target modification | Ecotype/Strain | Biotype | Biotype modification | Source | Species | Experiment | Peaks |