DDX20

Information DDX20

Description

DEAD box proteins, characterized by the conserved motif Asp-Glu-Ala-Asp (DEAD), are putative RNA helicases. They are implicated in a number of cellular processes involving alteration of RNA secondary structure such as translation initiation, nuclear and mitochondrial splicing, and ribosome and spliceosome assembly. Based on their distribution patterns, some members of this family are believed to be involved in embryogenesis, spermatogenesis, and cellular growth and division. This gene encodes a DEAD box protein, which has an ATPase activity and is a component of the survival of motor neurons (SMN) complex. This protein interacts directly with SMN, the spinal muscular atrophy gene product, and may play a catalytic role in the function of the SMN complex on RNPs. [provided by RefSeq, Jul 2008]

Full Name

DEAD-box helicase 20

Source NCBI

ReMap Statistics

Datasets
3
Biotypes
2
Peaks
15,238
Non-redundant peaks
13,647

TF Classification

Super Class
Unknown
Class
Unknown
Familly
Unknown
Sub Familly
Unknown

Source TFClass

External IDs

JASPAR
Ensembl
ENSG00000064703
UniProt
Q9UHI6
Genevisible
Q9UHI6
RefSeq
NM_007204
Aliases
DP103; GEMIN3
All peaks DDX20
Download BED file
Non redundant peaks DDX20
Download BED file
SEQUENCES DDX20
Download FASTA file
DOWNLOAD All ReMap
Got to catalogue

Datasets Table for DDX20

Target name Target modification Ecotype/Strain Biotype Biotype modification Source Species Experiment Peaks
DDX20 K-562 ENCODE Homo sapiens ENCSR382AIB 3,607
DDX20 K-562 ENCODE Homo sapiens ENCSR446LAV 9,856
DDX20 MCF-7 ENCODE Homo sapiens ENCSR330ADN 1,775
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.