ZNF778
Information ZNF778
- Description
The protein encoded by this gene is a member of the krueppel C2H2-type zinc-finger protein family, and it contains one KRAB domain and eighteen C2H2-type zinc fingers. This gene is a candidate gene for autism and variable cognitive impairment in the 16q24.3 microdeletion syndrome. Alternatively spliced transcript variants have been found for this gene. [provided by RefSeq, Jan 2011]
- Full Name
zinc finger protein 778
- Source NCBI
ReMap Statistics
- Datasets
- 2
- Biotypes
- 2
- Peaks
- 17,311
- Non-redundant peaks
- 16,189
TF Classification
- Super Class
- NA
- Class
- NA
- Familly
- NA
- Sub Familly
- NA
Source TFClass
External IDs
- JASPAR
- Ensembl
- ENSG00000170100
- UniProt
- Q96MU6
- Genevisible
- Q96MU6
- RefSeq
- NM_001201407
- Aliases
- FLJ31875
Datasets Table for ZNF778
| Target name | Target modification | Ecotype/Strain | Biotype | Biotype modification | Source | Species | Experiment | Peaks |
|---|---|---|---|---|---|---|---|---|
| ZNF778 | HEK293 | GEO | Homo sapiens | GSE76494 | 10,672 | |||
| ZNF778 | HEK293T | GEO | Homo sapiens | GSE78099 | 6,639 | |||
| Target name | Target modification | Ecotype/Strain | Biotype | Biotype modification | Source | Species | Experiment | Peaks |