OGG1
N-glycosylase/DNA lyase
Also known as: HMMH, HOGG1, MUTM, OGG1_HUMAN, OGH1
Cross-references: UniProt · Ensembl · Human Protein Atlas · GeneCards · NCBI Gene
Protein identityUniProt · HPA
- UniProt accession
- O15527
- Gene
- OGG1
- Ensembl
- ENSG00000114026
- Chromosome
- 3
- Canonical length
- 345 aa
- Protein class
- Cancer-related genes, Disease related genes, Enzymes, Human disease related genes, Plasma proteins, Potential drug targets, Predicted intracellular proteins
- Subcellular location
- Nucleoplasm
OverviewNCBI Gene
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]
Canonical amino-acid sequenceUniProt
345 residues, UniProt reviewed canonical sequence.
>O15527|OGG1
1 MPARALLPRR MGHRTLASTP ALWASIPCPR SELRLDLVLP SGQSFRWREQ SPAHWSGVLA
61 DQVWTLTQTE EQLHCTVYRG DKSQASRPTP DELEAVRKYF QLDVTLAQLY HHWGSVDSHF
121 QEVAQKFQGV RLLRQDPIEC LFSFICSSNN NIARITGMVE RLCQAFGPRL IQLDDVTYHG
181 FPSLQALAGP EVEAHLRKLG LGYRARYVSA SARAILEEQG GLAWLQQLRE SSYEEAHKAL
241 CILPGVGTKV ADCICLMALD KPQAVPVDVH MWHIAQRDYS WHPTTSQAKG PSPQTNKELG
301 NFFRSLWGPY AGWAQAVLFS ADLRQSRHAQ EPPAKRRKGS KGPEGLocalizationUniProt · AlphaFold · HPA
Whether an antibody against OGG1 can act on the native protein depends on physical access: surface and secreted proteins are reachable by circulating antibodies, intracellular proteins usually are not.
- Antibody reachability
- Intracellular
- Secreted
- No
- Transmembrane segments
- 0
- Mean surface accessibility (rSASA)
- 0.28
- Highest tissue expression
- 26 nTPM
Expression across tissuesHPA
Tissue
- kidney: 26 nTPM
- lymph node: 24 nTPM
- tonsil: 20 nTPM
- ovary: 19 nTPM
- liver: 18 nTPM
- duodenum: 18 nTPM
Single-cell type
- adipocytes: 74 nCPM
- epicardial cells: 59 nCPM
- enterocytes: 55 nCPM
- proximal tubule cells: 52 nCPM
- retinal ganglion cells: 46 nCPM
- megakaryocytes: 43 nCPM
Immune cell
- NK-cell: 28 nTPM
- T-reg: 22 nTPM
- eosinophil: 21 nTPM
- gdT-cell: 19 nTPM
- MAIT T-cell: 19 nTPM
- naive B-cell: 17 nTPM
Brain region
- cerebellum: 26 nTPM
- medulla oblongata: 25 nTPM
- hippocampal formation: 25 nTPM
- cerebral cortex: 24 nTPM
- amygdala: 23 nTPM
- basal ganglia: 22 nTPM
DiseaseUniProt · ClinVar · IEDB · PubMed
Four sources answering four different questions about OGG1.
Disease | AllUniProt
Conditions OGG1 is implicated in, by any mechanism.
- Renal cell carcinoma (RCC) MIM:144700
Genetic constraint and essentialitygnomAD · DepMap
Does the body need this protein intact? Low LOEUF or a strong DepMap dependency means loss or blockade of the protein is likely to be felt.
- gnomAD LOEUF (loss-of-function intolerance)
- 1.3
- gnomAD pLI
- 0
- gnomAD missense Z
- -0.57
- DepMap mean gene effect
- 0.12
- DepMap dependency class
- none
Cancer expressionTCGA
Across TCGA tumor cohorts, this protein is over-expressed in roughly 4% of surveyed tumor types (aggregate summary; per-cohort expression, alteration, and survival load in the interactive view).
OntologyGO
Biological processes
- base-excision repair
- base-excision repair, AP site formation
- cellular response to reactive oxygen species
- depurination
- depyrimidination
- DNA damage response
- nucleotide-excision repair
- positive regulation of gene expression via chromosomal CpG island demethylation
- positive regulation of transcription by RNA polymerase II
- regulation of DNA-templated transcription
- response to oxidative stress
- response to radiation
- negative regulation of double-strand break repair via single-strand annealing
Molecular functions
- 8-oxo-7,8-dihydroguanine DNA N-glycosylase activity
- class I DNA-(apurinic or apyrimidinic site) endonuclease activity
- damaged DNA binding
- DNA binding
- endonuclease activity
- enzyme binding
- microtubule binding
- oxidized purine DNA binding
- oxidized purine nucleobase lesion DNA N-glycosylase activity
- RNA polymerase II cis-regulatory region sequence-specific DNA binding
Cellular components
Protein domainsUniProt · Pfam · InterPro
- HhH-GPD domain
- DNA glycosylase
- Helix-hairpin-helix, base-excision DNA repair, C-terminal
- HhH-GPD superfamily base excision DNA repair protein
- 8-oxoguanine DNA-glycosylase
- 8-oxoguanine DNA glycosylase, N-terminal
- Oxidative DNA damage repair enzyme
- 8-oxoguanine DNA glycosylase, N-terminal domain
KeywordsUniProt
InteractionsUniProt · HPA
Protein binding partners of OGG1 in the human serome: UniProt-annotated complex subunits plus reported interactors. Each links to its own Seroatlas record.
Antibody and autoantibody relevanceSeroatlas analysis
Seroatlas reads OGG1 as an antibody target. Whether an autoantibody or antibody against OGG1 could matter depends on whether native OGG1 is physically reachable, whether the body needs it intact, and whether it acts in a disease-relevant tissue.
OGG1 is annotated as predominantly intracellular. Intracellular proteins are common autoantibody markers, becoming visible to the immune system after cell injury or altered processing, but are usually markers of disease rather than direct drivers.
Annotation status
The present source text does not explicitly label OGG1 as an autoantigen. Seroatlas presents hypothesis context only and does not manufacture a known-serology claim.
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