CEBPG

Information CEBPG

Description

The C/EBP family of transcription factors regulates viral and cellular CCAAT/enhancer element-mediated transcription. C/EBP proteins contain the bZIP region, which is characterized by two motifs in the C-terminal half of the protein: a basic region involved in DNA binding and a leucine zipper motif involved in dimerization. The C/EBP family consist of several related proteins, C/EBP alpha, C/EBP beta, C/EBP gamma, and C/EBP delta, that form homodimers and that form heterodimers with each other. CCAAT/enhancer binding protein gamma may cooperate with Fos to bind PRE-I enhancer elements. Two transcript variants encoding the same protein have been found for this gene. [provided by RefSeq, Nov 2011]

Full Name

CCAAT enhancer binding protein gamma

Source NCBI

ReMap Statistics

Datasets
4
Biotypes
3
Peaks
194,141
Non-redundant peaks
149,252

TF Classification

Super Class
Basic domains
Class
Basic leucine zipper factors (bZIP)
Familly
C/EBP-related
Sub Familly
C/EBP

Source TFClass

External IDs

JASPAR
MA0838
Ensembl
ENSG00000153879
UniProt
P53567
Genevisible
P53567
RefSeq
NM_001252296
Aliases
GPE1BP; IG/EBP-1
All peaks CEBPG
Download BED file
Non redundant peaks CEBPG
Download BED file
SEQUENCES CEBPG
Download FASTA file
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Datasets Table for CEBPG

Target name Target modification Ecotype/Strain Biotype Biotype modification Source Species Experiment Peaks
CEBPG Hep-G2 ENCODE Homo sapiens ENCSR639IIZ 111,819
CEBPG K-562 ENCODE Homo sapiens ENCSR490LWA 47,867
CEBPG K-562 ENCODE Homo sapiens ENCSR620VIC 29,648
CEBPG MCF-7 ENCODE Homo sapiens ENCSR094ZCF 4,807
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.