ETV6

Information ETV6

Description

This gene encodes an ETS family transcription factor. The product of this gene contains two functional domains: a N-terminal pointed (PNT) domain that is involved in protein-protein interactions with itself and other proteins, and a C-terminal DNA-binding domain. Gene knockout studies in mice suggest that it is required for hematopoiesis and maintenance of the developing vascular network. This gene is known to be involved in a large number of chromosomal rearrangements associated with leukemia and congenital fibrosarcoma. [provided by RefSeq, Sep 2008]

Full Name

ETS variant 6

Source NCBI

ReMap Statistics

Datasets
6
Biotypes
3
Peaks
81,276
Non-redundant peaks
54,941

TF Classification

Super Class
Helix-turn-helix domains
Class
Tryptophan cluster factors
Familly
Ets-related factors
Sub Familly
ETV6-like factors

Source TFClass

External IDs

JASPAR
MA0645
Ensembl
ENSG00000139083
UniProt
P41212
Genevisible
P41212
RefSeq
NM_001987
Aliases
TEL; TEL/ABL; THC5
All peaks ETV6
Download BED file
Non redundant peaks ETV6
Download BED file
SEQUENCES ETV6
Download FASTA file
DOWNLOAD All ReMap
Got to catalogue

Datasets Table for ETV6

Target name Target modification Ecotype/Strain Biotype Biotype modification Source Species Experiment Peaks
ETV6 GM12878 ENCODE Homo sapiens ENCSR597VGC 6,117
ETV6 GM12878 ENCODE Homo sapiens ENCSR626VUC 26,696
ETV6 K-562 ENCODE Homo sapiens ENCSR000FCE 4,569
ETV6 K-562 ENCODE Homo sapiens ENCSR124BJR 6,720
ETV6 Reh pCCL-ETV6-HA GEO Homo sapiens GSE102785 7,329
ETV6 GM12878 GEO Homo sapiens GSE97661 29,845
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.