CBX3

Information CBX3

Description

At the nuclear envelope, the nuclear lamina and heterochromatin are adjacent to the inner nuclear membrane. The protein encoded by this gene binds DNA and is a component of heterochromatin. This protein also can bind lamin B receptor, an integral membrane protein found in the inner nuclear membrane. The dual binding functions of the encoded protein may explain the association of heterochromatin with the inner nuclear membrane. This protein binds histone H3 tails methylated at Lys-9 sites. This protein is also recruited to sites of ultraviolet-induced DNA damage and double-strand breaks. Two transcript variants encoding the same protein but differing in the 5' UTR, have been found for this gene.[provided by RefSeq, Mar 2011]

Full Name

chromobox 3

Source NCBI

ReMap Statistics

Datasets
5
Biotypes
3
Peaks
123,476
Non-redundant peaks
112,539

TF Classification

Super Class
Unknown
Class
Unknown
Familly
Unknown
Sub Familly
Unknown

Source TFClass

External IDs

JASPAR
Ensembl
ENSG00000122565
UniProt
Q13185
Genevisible
Q13185
RefSeq
NM_007276
Aliases
HECH; HP1-GAMMA; HP1Hs-gamma
All peaks CBX3
Download BED file
Non redundant peaks CBX3
Download BED file
SEQUENCES CBX3
Download FASTA file
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Datasets Table for CBX3

Target name Target modification Ecotype/Strain Biotype Biotype modification Source Species Experiment Peaks
CBX3 K-562 ENCODE Homo sapiens ENCSR000ATV 296
CBX3 K-562 ENCODE Homo sapiens ENCSR000BRT 93,758
CBX3 HCT-116 ENCODE Homo sapiens ENCSR000BUH 27,745
CBX3 T-47D-MTVL GEO Homo sapiens GSE64467 1,307
CBX3 T-47D-MTVL BPTF GEO Homo sapiens GSE64467 370
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.