Bos taurus Gene: OGG1
Summary
InnateDB Gene IDBG-644719.3
Last Modified 2014-10-13 [Report errors or provide feedback]
Gene Symbol OGG1
Gene Name N-glycosylase/DNA lyase
Synonyms
Species Bos taurus
Ensembl Gene ENSBTAG00000007777
Encoded Proteins
N-glycosylase/DNA lyase
Protein Structure
Useful resources Stemformatics EHFPI ImmGen
Entrez Gene
Summary This gene does not have any Entrez summary - the following is the summary from its human ortholog ENSG00000114026:
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]
Gene Information
Type Protein coding
Genomic Location Chromosome 22:17001861-17007470
Strand Reverse strand
Band
Transcripts
ENSBTAT00000010226 ENSBTAP00000010226
Interactions
Number of Interactions This gene and/or its encoded proteins are associated with 0 experimentally validated interaction(s) in this database.
They are also associated with 9 interaction(s) predicted by orthology.
Predicted by orthology
Total 9 [view]
Gene Ontology

Molecular Function
Accession GO Term
GO:0003684 damaged DNA binding
GO:0003824 catalytic activity
GO:0005515 protein binding
GO:0008017 microtubule binding
GO:0008534 oxidized purine nucleobase lesion DNA N-glycosylase activity
GO:0034039 8-oxo-7,8-dihydroguanine DNA N-glycosylase activity
Biological Process
GO:0000737 DNA catabolic process, endonucleolytic
GO:0006281 DNA repair
GO:0006284 base-excision repair
GO:0006289 nucleotide-excision repair
GO:0006355 regulation of transcription, DNA-templated
GO:0006979 response to oxidative stress
GO:0009314 response to radiation
GO:0033158 regulation of protein import into nucleus, translocation
Cellular Component
GO:0005634 nucleus
GO:0005654 nucleoplasm
GO:0005739 mitochondrion
GO:0016363 nuclear matrix
GO:0016607 nuclear speck
Orthologs
Species
Homo sapiens
Mus musculus
Gene ID
Gene Order
Pathway Predictions based on Human Orthology Data
NETPATH
REACTOME
Displacement of DNA glycosylase by APE1 pathway
Base-free sugar-phosphate removal via the single-nucleotide replacement pathway pathway
Resolution of AP sites via the single-nucleotide replacement pathway pathway
Removal of DNA patch containing abasic residue pathway
Resolution of AP sites via the multiple-nucleotide patch replacement pathway pathway
Recognition and association of DNA glycosylase with site containing an affected purine pathway
Cleavage of the damaged purine pathway
Resolution of Abasic Sites (AP sites) pathway
Base Excision Repair pathway
Base-Excision Repair, AP Site Formation pathway
Depurination pathway
DNA Repair pathway
Base-free sugar-phosphate removal via the single-nucleotide replacement pathway pathway
Displacement of DNA glycosylase by APE1 pathway
Resolution of AP sites via the single-nucleotide replacement pathway pathway
Base Excision Repair pathway
Base-Excision Repair, AP Site Formation pathway
Resolution of AP sites via the multiple-nucleotide patch replacement pathway pathway
Depurination pathway
DNA Repair pathway
Removal of DNA patch containing abasic residue pathway
Cleavage of the damaged purine pathway
Resolution of Abasic Sites (AP sites) pathway
Recognition and association of DNA glycosylase with site containing an affected purine pathway
KEGG
Base excision repair pathway
Base excision repair pathway
INOH
PID NCI
Validated transcriptional targets of TAp63 isoforms
Cross-References
SwissProt
TrEMBL A1L536 F1MPV2
UniProt Splice Variant
Entrez Gene 520497
UniGene
RefSeq NM_001080285 XM_005222462 XM_005222463
HUGO
OMIM
CCDS
HPRD
IMGT
EMBL BT029823 DAAA02053758
GenPept ABM06086
RNA Seq Atlas 520497