ARID2

Information ARID2

Description

This gene encodes a member of the AT-rich interactive domain (ARID)-containing family of DNA-binding proteins. Members of the ARID family have roles in embryonic patterning, cell lineage gene regulation, cell cycle control, transcriptional regulation and chromatin structure modification. This protein functions as a subunit of the polybromo- and BRG1-associated factor or PBAF (SWI/SNF-B) chromatin remodeling complex which facilitates ligand-dependent transcriptional activation by nuclear receptors. Mutations in this gene are associated with hepatocellular carcinomas. A pseudogene of this gene is found on chromosome1. [provided by RefSeq, Dec 2016]

Full Name

AT-rich interaction domain 2

Source NCBI

ReMap Statistics

Datasets
4
Biotypes
3
Peaks
110,624
Non-redundant peaks
87,204

TF Classification

Super Class
Helix-turn-helix domains
Class
ARID domain factors
Familly
ARID-related factors
Sub Familly
ARID2

Source TFClass

External IDs

JASPAR
Ensembl
ENSG00000189079
UniProt
Q68CP9
Genevisible
Q68CP9
RefSeq
NM_001347839
Aliases
BAF200; DKFZp686G052; FLJ30619; KIAA1557
All peaks ARID2
Download BED file
Non redundant peaks ARID2
Download BED file
SEQUENCES ARID2
Download FASTA file
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Datasets Table for ARID2

Target name Target modification Ecotype/Strain Biotype Biotype modification Source Species Experiment Peaks
ARID2 Aska-SS GEO Homo sapiens GSE108025 34,024
ARID2 Aska-SS shSSX GEO Homo sapiens GSE108025 45,178
ARID2 K-562 ENCODE Homo sapiens ENCSR491EBY 9,889
ARID2 Hep-G2 GEO Homo sapiens GSE69566 21,533
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.