DMAP1

Information DMAP1

Description

This gene encodes a subunit of several, distinct complexes involved in the repression or activation of transcription. The encoded protein can independently repress transcription and is targeted to replication foci throughout S phase by interacting directly with the N-terminus of DNA methyltransferase 1. During late S phase, histone deacetylase 2 is added to this complex, providing a means to deacetylate histones in transcriptionally inactive heterochromatin following replication. The encoded protein is also a component of the nucleosome acetyltransferase of H4 complex and interacts with the transcriptional corepressor tumor susceptibility gene 101 and the pro-apoptotic death-associated protein 6, among others. Alternatively spliced transcript variants encoding the same protein have been described. [provided by RefSeq, Jul 2008]

Full Name

DNA methyltransferase 1 associated protein 1

Source NCBI

ReMap Statistics

Datasets
1
Biotypes
1
Peaks
47,981
Non-redundant peaks
47,981

TF Classification

Super Class
NA
Class
NA
Familly
NA
Sub Familly
NA

Source TFClass

External IDs

JASPAR
Ensembl
ENSG00000178028
UniProt
Q9NPF5
Genevisible
Q9NPF5
RefSeq
NM_001034023
Aliases
DNMAP1; DNMTAP1; EAF2; FLJ11543; KIAA1425; MEAF2; SWC4
All peaks DMAP1
Download BED file
Non redundant peaks DMAP1
Download BED file
SEQUENCES DMAP1
Download FASTA file
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Datasets Table for DMAP1

Target name Target modification Ecotype/Strain Biotype Biotype modification Source Species Experiment Peaks
DMAP1 Hep-G2 ENCODE Homo sapiens ENCSR670YPQ 47,981
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.