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About: Cytochrome c oxidase subunit I     Goto   Sponge   NotDistinct   Permalink

An Entity of Type : yago:WikicatProteinDomains, within Data Space : dbpedia.org associated with source document(s)

Type: ThingBiomoleculegeneBiomoleculeGeneyago:WikicatTransmembraneProteinsyago:Abstraction100002137yago:Attribute100024264yago:Chemical114806838yago:Compound114818238yago:Environment113934596yago:Macromolecule114944888yago:Material114580897yago:Matter100020827yago:Molecule114682133yago:OrganicCompound114727670yago:Part113809207yago:PhysicalEntity100001930yago:Protein114728724yago:Relation100031921HumanGeneyago:Situation113927383yago:Sphere114514039yago:State100024720yago:Substance100019613yago:Thing100002452yago:Unit109465459yago:WikicatProteinDomains New Facet based on Instances of this Class

Cytochrome c oxidase I (COX1) also known as mitochondrially encoded cytochrome c oxidase I (MT-CO1) is a protein that in humans is encoded by the MT-CO1 gene. In other eukaryotes, the gene is called COX1, CO1, or COI. Cytochrome c oxidase I is the main subunit of the cytochrome c oxidase complex. Mutations in MT-CO1 have been associated with Leber's hereditary optic neuropathy (LHON), acquired idiopathic sideroblastic anemia, Complex IV deficiency, colorectal cancer, sensorineural deafness, and recurrent myoglobinuria.