NCOR2

Information NCOR2

Description

This gene encodes a nuclear receptor co-repressor that mediates transcriptional silencing of certain target genes. The encoded protein is a member of a family of thyroid hormone- and retinoic acid receptor-associated co-repressors. This protein acts as part of a multisubunit complex which includes histone deacetylases to modify chromatin structure that prevents basal transcriptional activity of target genes. Aberrant expression of this gene is associated with certain cancers. Alternate splicing results in multiple transcript variants encoding different isoforms.[provided by RefSeq, Apr 2011]

Full Name

nuclear receptor corepressor 2

Source NCBI

ReMap Statistics

Datasets
4
Biotypes
3
Peaks
64,813
Non-redundant peaks
60,443

TF Classification

Super Class
Helix-turn-helix domains
Class
Tryptophan cluster factors
Familly
Myb/SANT domain factors
Sub Familly
NCoR-like factors

Source TFClass

External IDs

JASPAR
Ensembl
ENSG00000196498
UniProt
Q9Y618
Genevisible
Q9Y618
RefSeq
NM_001077261
Aliases
CTG26; N-CoR2; SMAP270; SMRT; SMRTE; SMRTE-tau; TNRC14; TRAC; TRAC-1; TRAC1
All peaks NCOR2
Download BED file
Non redundant peaks NCOR2
Download BED file
SEQUENCES NCOR2
Download FASTA file
DOWNLOAD All ReMap
Got to catalogue

Datasets Table for NCOR2

Target name Target modification Ecotype/Strain Biotype Biotype modification Source Species Experiment Peaks
NCOR2 LS180 GEO Homo sapiens GSE39277 17,156
NCOR2 LS180 125 GEO Homo sapiens GSE39277 29,423
NCOR2 OCI-Ly1 GEO Homo sapiens GSE29282 7,715
NCOR2 B-cell GERMINAL_CENTER GEO Homo sapiens GSE43350 10,519
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.