COX16
Cytochrome c oxidase assembly protein COX16 homolog, mitochondrial
Also known as: C14orf112, COX16_HUMAN, HSPC203
Cross-references: UniProt · Ensembl · Human Protein Atlas · GeneCards · NCBI Gene
Protein identityUniProt · HPA
- UniProt accession
- Q9P0S2
- Gene
- COX16
- Ensembl
- ENSG00000133983
- Chromosome
- 14
- Canonical length
- 106 aa
- Protein class
- Disease related genes, Human disease related genes, Potential drug targets, Predicted intracellular proteins, Transporters
- Subcellular location
- Mitochondria
OverviewNCBI Gene
Involved in mitochondrial cytochrome c oxidase assembly. Located in mitochondrial inner membrane. Implicated in mitochondrial complex IV deficiency nuclear type 22. [provided by Alliance of Genome Resources, Jul 2025]
Canonical amino-acid sequenceUniProt
106 residues, UniProt reviewed canonical sequence.
>Q9P0S2|COX16
1 MFAPAVMRAF RKNKTLGYGV PMLLLIVGGS FGLREFSQIR YDAVKSKMDP ELEKKLKENK
61 ISLESEYEKI KDSKFDDWKN IRGPRPWEDP DLLQGRNPES LKTKTTLocalizationUniProt · AlphaFold · HPA
Whether an antibody against COX16 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)
- 0.53
- Highest tissue expression
- 79 nTPM
Expression across tissuesHPA
Tissue
- skeletal muscle: 79 nTPM
- tongue: 42 nTPM
- pancreas: 41 nTPM
- liver: 38 nTPM
- kidney: 32 nTPM
- choroid plexus: 32 nTPM
Single-cell type
- parietal cells: 147 nCPM
- oocytes: 124 nCPM
- gastric chief cells: 94 nCPM
- mucous neck cells: 57 nCPM
- endometrial luminal cells: 55 nCPM
- other brain neurons: 52 nCPM
Immune cell
- plasmacytoid DC: 56 nTPM
- basophil: 49 nTPM
- memory B-cell: 45 nTPM
- NK-cell: 45 nTPM
- total PBMC: 44 nTPM
- T-reg: 43 nTPM
Brain region
- choroid plexus: 21 nTPM
- white matter: 20 nTPM
- medulla oblongata: 18 nTPM
- hypothalamus: 17 nTPM
- cerebral cortex: 17 nTPM
- cerebellum: 16 nTPM
DiseaseUniProt · ClinVar · IEDB · PubMed
Four sources answering four different questions about COX16.
Disease | AllUniProt
Conditions COX16 is implicated in, by any mechanism.
- Mitochondrial complex IV deficiency, nuclear type 22 (MC4DN22) MIM:619355
Disease | GeneticClinVar
2 pathogenic / likely-pathogenic of 19 ClinVar records.
Conditions with pathogenic or likely-pathogenic variants.
- Mitochondrial complex IV deficiency, nuclear type 22
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)
- 1.78
- gnomAD pLI
- 0
- gnomAD missense Z
- 0.25
- DepMap mean gene effect
- -0.01
- 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 protein COX16
- Cytochrome c oxidase assembly protein COX16
KeywordsUniProt
InteractionsUniProt · HPA
Protein binding partners of COX16 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 COX16 as an antibody target. Whether an autoantibody or antibody against COX16 could matter depends on whether native COX16 is physically reachable, whether the body needs it intact, and whether it acts in a disease-relevant tissue.
COX16 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 COX16 as an autoantigen. Seroatlas presents hypothesis context only and does not manufacture a known-serology claim.
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