AGO1

Information AGO1

Description

This gene encodes a member of the argonaute family of proteins, which associate with small RNAs and have important roles in RNA interference (RNAi) and RNA silencing. This protein binds to microRNAs (miRNAs) or small interfering RNAs (siRNAs) and represses translation of mRNAs that are complementary to them. It is also involved in transcriptional gene silencing (TGS) of promoter regions that are complementary to bound short antigene RNAs (agRNAs), as well as in the degradation of miRNA-bound mRNA targets. Alternatively spliced transcript variants encoding different isoforms have been found for this gene. A recent study showed this gene to be an authentic stop codon readthrough target, and that its mRNA could give rise to an additional C-terminally extended isoform by use of an alternative in-frame translation termination codon. [provided by RefSeq, Nov 2015]

Full Name

argonaute RISC component 1

Source NCBI

ReMap Statistics

Datasets
2
Biotypes
2
Peaks
84,177
Non-redundant peaks
72,130

TF Classification

Super Class
NA
Class
NA
Familly
NA
Sub Familly
NA

Source TFClass

External IDs

JASPAR
Ensembl
ENSG00000092847
UniProt
Q9UL18
Genevisible
Q9UL18
RefSeq
NM_001317122
Aliases
EIF2C; EIF2C1; GERP95; Q99; hAGO1; hAgo1
All peaks AGO1
Download BED file
Non redundant peaks AGO1
Download BED file
SEQUENCES AGO1
Download FASTA file
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Datasets Table for AGO1

Target name Target modification Ecotype/Strain Biotype Biotype modification Source Species Experiment Peaks
AGO1 Hep-G2 ENCODE Homo sapiens ENCSR555ZMV 60,698
AGO1 K-562 ENCODE Homo sapiens ENCSR641BSL 23,479
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.