CBFA2T3

Information CBFA2T3

Description

This gene encodes a member of the myeloid translocation gene family which interact with DNA-bound transcription factors and recruit a range of corepressors to facilitate transcriptional repression. The t(16;21)(q24;q22) translocation is one of the less common karyotypic abnormalities in acute myeloid leukemia. The translocation produces a chimeric gene made up of the 5'-region of the runt-related transcription factor 1 gene fused to the 3'-region of this gene. This gene is also a putative breast tumor suppressor. Alternative splicing results in transcript variants. [provided by RefSeq, Nov 2010]

Full Name

CBFA2/RUNX1 partner transcriptional co-repressor 3

Source NCBI

ReMap Statistics

Datasets
1
Biotypes
1
Peaks
55,031
Non-redundant peaks
55,031

TF Classification

Super Class
NA
Class
NA
Familly
NA
Sub Familly
NA

Source TFClass

External IDs

JASPAR
Ensembl
ENSG00000129993
UniProt
O75081
Genevisible
O75081
RefSeq
NM_005187
Aliases
ETO2; MTG16; MTGR2; RUNX1T3; ZMYND4
All peaks CBFA2T3
Download BED file
Non redundant peaks CBFA2T3
Download BED file
SEQUENCES CBFA2T3
Download FASTA file
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Datasets Table for CBFA2T3

Target name Target modification Ecotype/Strain Biotype Biotype modification Source Species Experiment Peaks
CBFA2T3 K-562 ENCODE Homo sapiens ENCSR697YLJ 55,031
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.