SMARCE1

Information SMARCE1

Description

The protein encoded by this gene is part of the large ATP-dependent chromatin remodeling complex SWI/SNF, which is required for transcriptional activation of genes normally repressed by chromatin. The encoded protein, either alone or when in the SWI/SNF complex, can bind to 4-way junction DNA, which is thought to mimic the topology of DNA as it enters or exits the nucleosome. The protein contains a DNA-binding HMG domain, but disruption of this domain does not abolish the DNA-binding or nucleosome-displacement activities of the SWI/SNF complex. Unlike most of the SWI/SNF complex proteins, this protein has no yeast counterpart. [provided by RefSeq, Jul 2008]

Full Name

SWI/SNF related, matrix associated, actin dependent regulator of chromatin, subfamily e, member 1

Source NCBI

ReMap Statistics

Datasets
4
Biotypes
4
Peaks
107,814
Non-redundant peaks
101,964

TF Classification

Super Class
NA
Class
NA
Familly
NA
Sub Familly
NA

Source TFClass

External IDs

JASPAR
Ensembl
ENSG00000073584
UniProt
Q969G3
Genevisible
Q969G3
RefSeq
NM_003079
Aliases
BAF57; CSS5
All peaks SMARCE1
Download BED file
Non redundant peaks SMARCE1
Download BED file
SEQUENCES SMARCE1
Download FASTA file
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Datasets Table for SMARCE1

Target name Target modification Ecotype/Strain Biotype Biotype modification Source Species Experiment Peaks
SMARCE1 Hep-G2 ENCODE Homo sapiens ENCSR968QDP 608
SMARCE1 K-562 ENCODE Homo sapiens ENCSR157TCS 63,058
SMARCE1 MCF-7 ENCODE Homo sapiens ENCSR431TLD 30,084
SMARCE1 HMLE-Twist-ER 125nM_4OHT GEO Homo sapiens GSE96933 14,064
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.