COX3 (gene)
From Wikipedia, the free encyclopedia
| It has been suggested that this article or section be merged with Cytochrome c oxidase subunit III. (Discuss) |
|
Cytochrome c oxidase subunit III
|
|||||
| Identifiers | |||||
| Symbol(s) | COX3; MTCO3 | ||||
| External IDs | MGI: 102502 HomoloGene: 5014 | ||||
|
|||||
| Orthologs | |||||
| Human | Mouse | ||||
| Entrez | 4514 | 17710 | |||
| Ensembl | ENSG00000198938 | ENSMUSG00000064358 | |||
| Uniprot | P00414 | Q5MCM2 | |||
| Refseq | n/a (mRNA) NP_536849 (protein) |
n/a (mRNA) NP_904334 (protein) |
|||
| Location | Chr MT: 0.01 - 0.01 Mb | Chr MT: 0.01 - 0.01 Mb | |||
| Pubmed search | [1] | [2] | |||
Cytochrome c oxidase subunit III, also known as COX3, is a human gene.[1]
[edit] References
[edit] Further reading
- Moraes CT, Andreetta F, Bonilla E, et al. (1991). "Replication-competent human mitochondrial DNA lacking the heavy-strand promoter region.". Mol. Cell. Biol. 11 (3): 1631–7. PMID 1996112.
- Chomyn A, Cleeter MW, Ragan CI, et al. (1986). "URF6, last unidentified reading frame of human mtDNA, codes for an NADH dehydrogenase subunit.". Science 234 (4776): 614–8. PMID 3764430.
- Chomyn A, Mariottini P, Cleeter MW, et al. (1985). "Six unidentified reading frames of human mitochondrial DNA encode components of the respiratory-chain NADH dehydrogenase.". Nature 314 (6012): 592–7. PMID 3921850.
- Anderson S, Bankier AT, Barrell BG, et al. (1981). "Sequence and organization of the human mitochondrial genome.". Nature 290 (5806): 457–65. PMID 7219534.
- Montoya J, Ojala D, Attardi G (1981). "Distinctive features of the 5'-terminal sequences of the human mitochondrial mRNAs.". Nature 290 (5806): 465–70. PMID 7219535.
- Andrews RM, Kubacka I, Chinnery PF, et al. (1999). "Reanalysis and revision of the Cambridge reference sequence for human mitochondrial DNA.". Nat. Genet. 23 (2): 147. doi:. PMID 10508508.
- Ingman M, Kaessmann H, Pääbo S, Gyllensten U (2001). "Mitochondrial genome variation and the origin of modern humans.". Nature 408 (6813): 708–13. doi:. PMID 11130070.
- Maca-Meyer N, González AM, Larruga JM, et al. (2003). "Major genomic mitochondrial lineages delineate early human expansions.". BMC Genet. 2: 13. PMID 11553319.
- Herrnstadt C, Elson JL, Fahy E, et al. (2002). "Reduced-median-network analysis of complete mitochondrial DNA coding-region sequences for the major African, Asian, and European haplogroups.". Am. J. Hum. Genet. 70 (5): 1152–71. PMID 11938495.
- Silva WA, Bonatto SL, Holanda AJ, et al. (2002). "Mitochondrial genome diversity of Native Americans supports a single early entry of founder populations into America.". Am. J. Hum. Genet. 71 (1): 187–92. PMID 12022039.
- Elkon H, Don J, Melamed E, et al. (2003). "Mutant and wild-type alpha-synuclein interact with mitochondrial cytochrome C oxidase.". J. Mol. Neurosci. 18 (3): 229–38. PMID 12059041.
- Mishmar D, Ruiz-Pesini E, Golik P, et al. (2003). "Natural selection shaped regional mtDNA variation in humans.". Proc. Natl. Acad. Sci. U.S.A. 100 (1): 171–6. doi:. PMID 12509511.
- Ingman M, Gyllensten U (2003). "Mitochondrial genome variation and evolutionary history of Australian and New Guinean aborigines.". Genome Res. 13 (7): 1600–6. doi:. PMID 12840039.
- Kong QP, Yao YG, Sun C, et al. (2003). "Phylogeny of east Asian mitochondrial DNA lineages inferred from complete sequences.". Am. J. Hum. Genet. 73 (3): 671–6. doi:. PMID 12870132.
- Temperley RJ, Seneca SH, Tonska K, et al. (2004). "Investigation of a pathogenic mtDNA microdeletion reveals a translation-dependent deadenylation decay pathway in human mitochondria.". Hum. Mol. Genet. 12 (18): 2341–8. doi:. PMID 12915481.
- Maca-Meyer N, González AM, Pestano J, et al. (2004). "Mitochondrial DNA transit between West Asia and North Africa inferred from U6 phylogeography.". BMC Genet. 4: 15. doi:. PMID 14563219.
- Coble MD, Just RS, O'Callaghan JE, et al. (2004). "Single nucleotide polymorphisms over the entire mtDNA genome that increase the power of forensic testing in Caucasians.". Int. J. Legal Med. 118 (3): 137–46. doi:. PMID 14760490.
- Palanichamy MG, Sun C, Agrawal S, et al. (2005). "Phylogeny of mitochondrial DNA macrohaplogroup N in India, based on complete sequencing: implications for the peopling of South Asia.". Am. J. Hum. Genet. 75 (6): 966–78. doi:. PMID 15467980.
- Starikovskaya EB, Sukernik RI, Derbeneva OA, et al. (2005). "Mitochondrial DNA diversity in indigenous populations of the southern extent of Siberia, and the origins of Native American haplogroups.". Ann. Hum. Genet. 69 (Pt 1): 67–89. doi:. PMID 15638829.
- Rajkumar R, Banerjee J, Gunturi HB, et al. (2006). "Phylogeny and antiquity of M macrohaplogroup inferred from complete mt DNA sequence of Indian specific lineages.". BMC Evol. Biol. 5 (1): 26. doi:. PMID 15804362.

