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
All peaks ZNF778
Download BED file
Non redundant peaks ZNF778
Download BED file
SEQUENCES ZNF778
Download FASTA file
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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

ReMap is a database of transcriptional regulators peaks derived from curated ChIP-seq, ChIP-exo, DAP-seq experiments in Human and Thaliana.

You are using the 2020 ReMap (3rd) release.
The ReMap catalogues (2020, 2018, 2015) are under CC BY-NC 4.0 international license, while ReMapEnrich, remap-pipeline under GNU GPLv3 licence.

Inserm TAGC
AMU AMU-MESO

This work was granted access to the HPC resources of Aix-Marseille Université financed by the project Equip@Meso (ANR-10-EQPX-29-01) of the program "Investissements d’Avenir" supervised by the Agence Nationale de la Recherche.