OGG1

Information OGG1

Description

This gene encodes the enzyme responsible for the excision of 8-oxoguanine, a mutagenic base byproduct which occurs as a result of exposure to reactive oxygen. The action of this enzyme includes lyase activity for chain cleavage. Alternative splicing of the C-terminal region of this gene classifies splice variants into two major groups, type 1 and type 2, depending on the last exon of the sequence. Type 1 alternative splice variants end with exon 7 and type 2 end with exon 8. All variants share the N-terminal region in common, which contains a mitochondrial targeting signal that is essential for mitochondrial localization. Many alternative splice variants for this gene have been described, but the full-length nature for every variant has not been determined. [provided by RefSeq, Aug 2008]

Full Name

8-oxoguanine DNA glycosylase

Source NCBI

ReMap Statistics

Datasets
4
Biotypes
1
Peaks
149,972
Non-redundant peaks
76,595

TF Classification

Super Class
NA
Class
NA
Familly
NA
Sub Familly
NA

Source TFClass

External IDs

JASPAR
Ensembl
ENSG00000114026
UniProt
O15527
Genevisible
O15527
RefSeq
NM_001354648
Aliases
HMMH; HOGG1; MUTM; OGH1
All peaks OGG1
Download BED file
Non redundant peaks OGG1
Download BED file
SEQUENCES OGG1
Download FASTA file
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Datasets Table for OGG1

Target name Target modification Ecotype/Strain Biotype Biotype modification Source Species Experiment Peaks
OGG1 HEK293 GEO Homo sapiens GSE89017 62,654
OGG1 HEK293 15min GEO Homo sapiens GSE89017 39,751
OGG1 HEK293 30_min GEO Homo sapiens GSE89017 15,382
OGG1 HEK293 60_min GEO Homo sapiens GSE89017 32,185
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.