DDX5

Information DDX5

Description

This gene encodes a member of the DEAD box family of RNA helicases that are involved in a variety of cellular processes as a result of its role as an adaptor molecule, promoting interactions with a large number of other factors. This protein is involved in pathways that include the alteration of RNA structures, plays a role as a coregulator of transcription, a regulator of splicing, and in the processing of small noncoding RNAs. Members of this family contain nine conserved motifs, including the conserved Asp-Glu-Ala-Asp (DEAD) motif, important to ATP binding and hydrolysis as well as RNA binding and unwinding activities. Dysregulation of this gene may play a role in cancer development. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Sep 2017]

Full Name

DEAD-box helicase 5

Source NCBI

ReMap Statistics

Datasets
2
Biotypes
2
Peaks
53,963
Non-redundant peaks
53,948

TF Classification

Super Class
Unknown
Class
Unknown
Familly
Unknown
Sub Familly
Unknown

Source TFClass

External IDs

JASPAR
Ensembl
ENSG00000108654
UniProt
P17844
Genevisible
P17844
RefSeq
NM_001320595
Aliases
G17P1; HLR1; HUMP68; p68
All peaks DDX5
Download BED file
Non redundant peaks DDX5
Download BED file
SEQUENCES DDX5
Download FASTA file
DOWNLOAD All ReMap
Got to catalogue

Datasets Table for DDX5

Target name Target modification Ecotype/Strain Biotype Biotype modification Source Species Experiment Peaks
DDX5 HeLa GEO Homo sapiens GSE24126 1,175
DDX5 NTERA2 GEO Homo sapiens GSE58641 52,788
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.