# Cytochrome c oxidase subunit I

> mammalian protein found in Mus musculus

**Wikidata**: [Q21984161](https://www.wikidata.org/wiki/Q21984161)  
**Source**: https://4ort.xyz/entity/cytochrome-c-oxidase-subunit-i-q21984161


## References

1. UniProt
2. [InterPro Release 71.0](http://www.ebi.ac.uk/interpro/protein/P00397)
3. Q20641742
4. [GOA](http://www.ebi.ac.uk/QuickGO/annotations?protein=P00397&geneProductId=UniProtKB:P00397)
5. [GOA](http://www.ebi.ac.uk/QuickGO/annotations?geneProductId=UniProtKB:P00397)
6. [Disruption of a mitochondrial RNA-binding protein gene results in decreased cytochrome b expression and a marked reduction in ubiquinol-cytochrome c reductase activity in mouse heart mitochondria](http://www.ebi.ac.uk/QuickGO/annotations?protein=P00397&geneProductId=UniProtKB:P00397)
7. [Disruption of a mitochondrial RNA-binding protein gene results in decreased cytochrome b expression and a marked reduction in ubiquinol-cytochrome c reductase activity in mouse heart mitochondria](http://www.ebi.ac.uk/QuickGO/annotations?geneProductId=UniProtKB:P00397)
8. [Phylogenetic-based propagation of functional annotations within the Gene Ontology consortium](http://www.ebi.ac.uk/QuickGO/annotations?geneProductId=UniProtKB:P00397)
9. [Pancreatic beta cells lack a low glucose and O2-inducible mitochondrial protein that augments cell survival](http://www.ebi.ac.uk/QuickGO/annotations?geneProductId=UniProtKB:P00397)
10. [A mitochondrial protein compendium elucidates complex I disease biology](http://www.ebi.ac.uk/QuickGO/annotations?protein=P00397&geneProductId=UniProtKB:P00397)
11. [Analysis of mouse models of cytochrome c oxidase deficiency owing to mutations in Sco2](http://www.ebi.ac.uk/QuickGO/annotations?protein=P00397&geneProductId=UniProtKB:P00397)
12. [Mice lacking COX10 in skeletal muscle recapitulate the phenotype of progressive mitochondrial myopathies associated with cytochrome c oxidase deficiency](http://www.ebi.ac.uk/QuickGO/annotations?protein=P00397&geneProductId=UniProtKB:P00397)
13. [Mitochondrial biogenesis and thyroid status maturation in brown fat require CCAAT/enhancer-binding protein alpha](http://www.ebi.ac.uk/QuickGO/annotations?protein=P00397&geneProductId=UniProtKB:P00397)
14. [Cloning and characterization of mouse mTERF encoding a mitochondrial transcriptional termination factor](http://www.ebi.ac.uk/QuickGO/annotations?protein=P00397&geneProductId=UniProtKB:P00397)
15. [Molecular characterization of mitocalcin, a novel mitochondrial Ca2+-binding protein with EF-hand and coiled-coil domains](http://www.ebi.ac.uk/QuickGO/annotations?protein=P00397&geneProductId=UniProtKB:P00397)
16. [Osteopontin inhibits expression of cytochrome c oxidase in RAW 264.7 murine macrophages](http://www.ebi.ac.uk/QuickGO/annotations?protein=P00397&geneProductId=UniProtKB:P00397)
17. [Partial complex I deficiency due to the CNS conditional ablation of Ndufa5 results in a mild chronic encephalopathy but no increase in oxidative damage](http://www.ebi.ac.uk/QuickGO/annotations?protein=P00397&geneProductId=UniProtKB:P00397)
18. [Osteopontin inhibits expression of cytochrome c oxidase in RAW 264.7 murine macrophages](http://www.ebi.ac.uk/QuickGO/annotations?geneProductId=UniProtKB:P00397)
19. [Mitochondrial biogenesis and thyroid status maturation in brown fat require CCAAT/enhancer-binding protein alpha](http://www.ebi.ac.uk/QuickGO/annotations?geneProductId=UniProtKB:P00397)
20. [Cloning and characterization of mouse mTERF encoding a mitochondrial transcriptional termination factor](http://www.ebi.ac.uk/QuickGO/annotations?geneProductId=UniProtKB:P00397)
21. [Molecular characterization of mitocalcin, a novel mitochondrial Ca2+-binding protein with EF-hand and coiled-coil domains](http://www.ebi.ac.uk/QuickGO/annotations?geneProductId=UniProtKB:P00397)
22. [Mice lacking COX10 in skeletal muscle recapitulate the phenotype of progressive mitochondrial myopathies associated with cytochrome c oxidase deficiency](http://www.ebi.ac.uk/QuickGO/annotations?geneProductId=UniProtKB:P00397)
23. [Analysis of mouse models of cytochrome c oxidase deficiency owing to mutations in Sco2](http://www.ebi.ac.uk/QuickGO/annotations?geneProductId=UniProtKB:P00397)
24. [A mitochondrial protein compendium elucidates complex I disease biology](http://www.ebi.ac.uk/QuickGO/annotations?geneProductId=UniProtKB:P00397)
25. [Partial complex I deficiency due to the CNS conditional ablation of Ndufa5 results in a mild chronic encephalopathy but no increase in oxidative damage](http://www.ebi.ac.uk/QuickGO/annotations?geneProductId=UniProtKB:P00397)
26. ensembl Release 106