COX7A2P2
Putative cytochrome c oxidase subunit 7A3, mitochondrial
Also known as: COX7S_HUMAN
Protein identityUniProt · HPA
OverviewNCBI Gene
No narrative summary is available for COX7A2P2 in this catalog release; identity and structured annotations are shown without generated factual claims.
Canonical amino-acid sequenceUniProt
106 residues, UniProt reviewed canonical sequence.
>O60397|COX7A2P2
1 MLWNLLALHQ IGQRTISTAS HRHFKNKVPE KQKLFQEDDG IPLYLKGGIA DALLHRATMI
61 LTVGGTAYAI YQLAVASFPN KGVTSIIPAI TWFTFIQLSM DQKSDKLocalizationUniProt · AlphaFold · HPA
Whether an antibody against COX7A2P2 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
- Other membrane
- Secreted
- No
- Transmembrane segments
- 0
- Mean surface accessibility (rSASA)
- 0.53
DiseaseUniProt · ClinVar · IEDB · PubMed
Four sources answering four different questions about COX7A2P2.
Disease | ImmuneIEDB
Conditions an epitope on COX7A2P2 was assayed in.
OntologyGO
Biological processes
- mitochondrial electron transport, cytochrome c to oxygen
- oxidative phosphorylation
- proton transmembrane transport
Cellular components
Protein domainsUniProt · Pfam · InterPro
KeywordsUniProt
Antibody and autoantibody relevanceSeroatlas analysis
Seroatlas reads COX7A2P2 as an antibody target. Whether an autoantibody or antibody against COX7A2P2 could matter depends on whether native COX7A2P2 is physically reachable, whether the body needs it intact, and whether it acts in a disease-relevant tissue.
COX7A2P2 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 COX7A2P2 as an autoantigen. Seroatlas presents hypothesis context only and does not manufacture a known-serology claim.
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