TCF7

Information TCF7

Description

This gene encodes a member of the T-cell factor/lymphoid enhancer-binding factor family of high mobility group (HMG) box transcriptional activators. This gene is expressed predominantly in T-cells and plays a critical role in natural killer cell and innate lymphoid cell development. The encoded protein forms a complex with beta-catenin and activates transcription through a Wnt/beta-catenin signaling pathway. Mice with a knockout of this gene are viable and fertile, but display a block in T-lymphocyte differentiation. Alternative splicing results in multiple transcript variants. Naturally-occurring isoforms lacking the N-terminal beta-catenin interaction domain may act as dominant negative regulators of Wnt signaling. [provided by RefSeq, Oct 2016]

Full Name

transcription factor 7

Source NCBI

ReMap Statistics

Datasets
3
Biotypes
3
Peaks
41,385
Non-redundant peaks
39,053

TF Classification

Super Class
Other all-alpha-helical DNA-binding domains
Class
High-mobility group (HMG) domain factors
Familly
TCF-7-related factors
Sub Familly
None

Source TFClass

External IDs

JASPAR
Ensembl
ENSG00000081059
UniProt
P36402
Genevisible
P36402
RefSeq
NM_001134851
Aliases
TCF-1
All peaks TCF7
Download BED file
Non redundant peaks TCF7
Download BED file
SEQUENCES TCF7
Download FASTA file
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Datasets Table for TCF7

Target name Target modification Ecotype/Strain Biotype Biotype modification Source Species Experiment Peaks
TCF7 GM12878 ENCODE Homo sapiens ENCSR501DKS 10,895
TCF7 Hep-G2 ENCODE Homo sapiens ENCSR444LIN 22,878
TCF7 K-562 ENCODE Homo sapiens ENCSR863KUB 7,612
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.