SMARCA2

Information SMARCA2

Description

The protein encoded by this gene is a member of the SWI/SNF family of proteins and is highly similar to the brahma protein of Drosophila. Members of this family have helicase and ATPase activities and are thought to regulate transcription of certain genes by altering the chromatin structure around those genes. The encoded protein is part of the large ATP-dependent chromatin remodeling complex SNF/SWI, which is required for transcriptional activation of genes normally repressed by chromatin. Alternatively spliced transcript variants encoding different isoforms have been found for this gene, which contains a trinucleotide repeat (CAG) length polymorphism. [provided by RefSeq, Jan 2014]

Full Name

SWI/SNF related, matrix associated, actin dependent regulator of chromatin, subfamily a, member 2

Source NCBI

ReMap Statistics

Datasets
2
Biotypes
1
Peaks
19,493
Non-redundant peaks
17,624

TF Classification

Super Class
NA
Class
NA
Familly
NA
Sub Familly
NA

Source TFClass

External IDs

JASPAR
Ensembl
ENSG00000080503
UniProt
P51531
Genevisible
P51531
RefSeq
NM_001289396
Aliases
BAF190; BRM; NCBRS; SNF2; SNF2L2; SNF2LA; SWI2; Sth1p; hBRM; hSNF2a
All peaks SMARCA2
Download BED file
Non redundant peaks SMARCA2
Download BED file
SEQUENCES SMARCA2
Download FASTA file
DOWNLOAD All ReMap
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Datasets Table for SMARCA2

Target name Target modification Ecotype/Strain Biotype Biotype modification Source Species Experiment Peaks
SMARCA2 SK-N-MC shEWSFLI1 GEO Homo sapiens GSE94275 15,923
SMARCA2 SK-N-MC shGFP GEO Homo sapiens GSE94275 3,570
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.