COA3
Cytochrome c oxidase assembly factor 3 homolog, mitochondrial
Also known as: CCDC56, COA3_HUMAN, COX25, hCOA3, HSPC009, MITRAC12
Cross-references: UniProt · Ensembl · Human Protein Atlas · GeneCards · NCBI Gene
Protein identityUniProt · HPA
- UniProt accession
- Q9Y2R0
- Gene
- COA3
- Ensembl
- ENSG00000183978
- Chromosome
- 17
- Canonical length
- 106 aa
- Protein class
- Disease related genes, Human disease related genes, Predicted membrane proteins
- Subcellular location
- Mitochondria
OverviewNCBI Gene
This gene encodes a member of the cytochrome c oxidase assembly factor family. Studies of a related gene in fly suggest that the encoded protein is localized to mitochondria and is essential for cytochrome c oxidase function. [provided by RefSeq, Nov 2012]
Canonical amino-acid sequenceUniProt
106 residues, UniProt reviewed canonical sequence.
>Q9Y2R0|COA3
1 MASSGAGDPL DSKRGEAPFA QRIDPTREKL TPEQLHSMRQ AELAQWQKVL PRRRTRNIVT
61 GLGIGALVLA IYGYTFYSIS QERFLDELED EAKAARARAL ARASGSLocalizationUniProt · AlphaFold · HPA
Whether an antibody against COA3 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
- 1
- Mean surface accessibility (rSASA)
- 0.56
- Highest tissue expression
- 266 nTPM
Expression across tissuesHPA
Tissue
- kidney: 266 nTPM
- pancreas: 163 nTPM
- epididymis: 163 nTPM
- liver: 152 nTPM
- amygdala: 133 nTPM
- cerebral cortex: 127 nTPM
Single-cell type
- esophageal suprabasal cells: 707 nCPM
- parietal cells: 654 nCPM
- esophageal apical cells: 568 nCPM
- hepatocytes: 414 nCPM
- esophageal basal cells: 386 nCPM
- epididymal principal cells: 383 nCPM
Immune cell
- total PBMC: 246 nTPM
- memory B-cell: 220 nTPM
- classical monocyte: 210 nTPM
- intermediate monocyte: 208 nTPM
- basophil: 208 nTPM
- T-reg: 192 nTPM
Brain region
- cerebellum: 61 nTPM
- pons: 58 nTPM
- thalamus: 57 nTPM
- choroid plexus: 56 nTPM
- midbrain: 56 nTPM
- spinal cord: 56 nTPM
DiseaseUniProt · ClinVar · IEDB · PubMed
Four sources answering four different questions about COA3.
Disease | AllUniProt
Conditions COA3 is implicated in, by any mechanism.
- Mitochondrial complex IV deficiency, nuclear type 14 (MC4DN14) MIM:619058
Disease | ImmuneIEDB
Conditions an epitope on COA3 was assayed in.
- skin melanoma T cell
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)
- 1.53
- gnomAD pLI
- 0.06
- gnomAD missense Z
- -0.19
- DepMap mean gene effect
- -0.29
- DepMap dependency class
- selective
Cancer expressionTCGA
Across TCGA tumor cohorts, this protein is over-expressed in roughly 5% of surveyed tumor types (aggregate summary; per-cohort expression, alteration, and survival load in the interactive view).
OntologyGO
Biological processes
Cellular components
Protein domainsUniProt · Pfam · InterPro
- Cytochrome c oxidase assembly factor 3, mitochondrial, coiled-coil domain
- Cytochrome c oxidase assembly factor 3, mitochondrial
- Cytochrome c oxidase assembly factor 3
KeywordsUniProt
InteractionsUniProt · HPA
Protein binding partners of COA3 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 COA3 as an antibody target. Whether an autoantibody or antibody against COA3 could matter depends on whether native COA3 is physically reachable, whether the body needs it intact, and whether it acts in a disease-relevant tissue.
COA3 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 COA3 as an autoantigen. Seroatlas presents hypothesis context only and does not manufacture a known-serology claim.
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