COX6C
Cytochrome c oxidase subunit 6C
Also known as: COX6C_HUMAN
Cross-references: UniProt · Ensembl · Human Protein Atlas · GeneCards · NCBI Gene
Protein identityUniProt · HPA
- UniProt accession
- P09669
- Gene
- COX6C
- Ensembl
- ENSG00000164919
- Chromosome
- 8
- Canonical length
- 75 aa
- Protein class
- Metabolic proteins, Predicted membrane proteins
- Subcellular location
- Mitochondria
OverviewNCBI Gene
Cytochrome c oxidase, the terminal enzyme of the mitochondrial respiratory chain, catalyzes the electron transfer from reduced cytochrome c to oxygen. It is a heteromeric complex consisting of 3 catalytic subunits encoded by mitochondrial genes and multiple structural subunits encoded by nuclear genes. The mitochondrially-encoded subunits function in electron transfer, and the nuclear-encoded subunits may be involved in the regulation and assembly of the complex. This nuclear gene encodes subunit VIc, which has 77% amino acid sequence identity with mouse subunit VIc. This gene is up-regulated in prostate cancer cells. A pseudogene has been found on chromosomes 16p12. [provided by RefSeq, Jul 2010]
Canonical amino-acid sequenceUniProt
75 residues, UniProt reviewed canonical sequence.
>P09669|COX6C
1 MAPEVLPKPR MRGLLARRLR NHMAVAFVLS LGVAALYKFR VADQRKKAYA DFYRNYDVMK
61 DFEEMRKAGI FQSVKLocalizationUniProt · AlphaFold · HPA
Whether an antibody against COX6C 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
- 727 nTPM
Expression across tissuesHPA
Tissue
- heart muscle: 727 nTPM
- skeletal muscle: 626 nTPM
- tongue: 516 nTPM
- amygdala: 420 nTPM
- cerebral cortex: 400 nTPM
- midbrain: 362 nTPM
Single-cell type
- parietal cells: 5,086 nCPM
- syncytiotrophoblasts: 2,329 nCPM
- hepatocytes: 2,107 nCPM
- decidual stromal cells: 2,066 nCPM
- enterocytes: 1,924 nCPM
- colonocytes: 1,633 nCPM
Immune cell
- basophil: 349 nTPM
- naive CD4 T-cell: 321 nTPM
- plasmacytoid DC: 303 nTPM
- naive CD8 T-cell: 296 nTPM
- T-reg: 274 nTPM
- memory CD4 T-cell: 272 nTPM
Brain region
- cerebral cortex: 140 nTPM
- hypothalamus: 111 nTPM
- thalamus: 108 nTPM
- hippocampal formation: 103 nTPM
- choroid plexus: 102 nTPM
- midbrain: 98 nTPM
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)
- 1.68
- gnomAD pLI
- 0.05
- gnomAD missense Z
- 0.08
- DepMap mean gene effect
- -0.4
- DepMap dependency class
- selective
Cancer expressionTCGA
Across TCGA tumor cohorts, this protein is over-expressed in roughly 11% of surveyed tumor types (aggregate summary; per-cohort expression, alteration, and survival load in the interactive view).
OntologyGO
Biological processes
- cellular respiration
- generation of precursor metabolites and energy
- mitochondrial electron transport, cytochrome c to oxygen
Cellular components
Protein domainsUniProt · Pfam · InterPro
- Mitochondrial cytochrome c oxidase subunit VIc/VIIs
- Mitochondrial cytochrome c oxidase subunit VIc/VIIs superfamily
- Cytochrome c oxidase subunit VIc
- Cytochrome c oxidase subunit VIc
KeywordsUniProt
InteractionsUniProt · HPA
Protein binding partners of COX6C 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 COX6C as an antibody target. Whether an autoantibody or antibody against COX6C could matter depends on whether native COX6C is physically reachable, whether the body needs it intact, and whether it acts in a disease-relevant tissue.
COX6C 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 COX6C as an autoantigen. Seroatlas presents hypothesis context only and does not manufacture a known-serology claim.
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