COX3 (gene)
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It has been suggested that this article be merged with Cytochrome c oxidase subunit III. (Discuss) Proposed since December 2007. |
Cytochrome c oxidase subunit III | |||||
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Identifiers | |||||
Symbols | COX3 ; MTCO3 | ||||
External IDs | Template:MGI HomoloGene: 5014 | ||||
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Orthologs | |||||
Template:GNF Ortholog box | |||||
Species | Human | Mouse | |||
Entrez | n/a | n/a | |||
Ensembl | n/a | n/a | |||
UniProt | n/a | n/a | |||
RefSeq (mRNA) | n/a | n/a | |||
RefSeq (protein) | n/a | n/a | |||
Location (UCSC) | n/a | n/a | |||
PubMed search | n/a | n/a |
Cytochrome c oxidase subunit III, also known as COX3, is a human gene.[1]
References
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:10.1038/13779. 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:10.1038/35047064. 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:10.1073/pnas.0136972100. 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:10.1101/gr.686603. 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:10.1086/377718. 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:10.1093/hmg/ddg238. 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:10.1186/1471-2156-4-15. 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:10.1007/s00414-004-0427-6. 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:10.1086/425871. 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:10.1046/j.1529-8817.2003.00127.x. 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:10.1186/1471-2148-5-26. PMID 15804362.
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