CYTB

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Cytochrome b
Identifiers
Symbol(s) CYTB; MTCYB
External IDs MGI: 102501 HomoloGene: 5013
Orthologs
Human Mouse
Entrez 4519 17711
Ensembl ENSG00000198727 ENSMUSG00000064370
Uniprot P00156 Q36290
Refseq n/a (mRNA)
NP_536855 (protein)		 n/a (mRNA)
NP_904340 (protein)
Location Chr MT: 0.01 - 0.02 Mb Chr MT: 0.01 - 0.02 Mb
Pubmed search [1] [2]

Cytochrome b, also known as CYTB, is a human gene.[1]


[edit] References

  1. ^ Entrez Gene: CYTB cytochrome b.

[edit] Further reading

  • 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. 
  • Yamasoba T, Goto Y, Oka Y, et al. (2002). "Atypical muscle pathology and a survey of cis-mutations in deaf patients harboring a 1555 A-to-G point mutation in the mitochondrial ribosomal RNA gene.". Neuromuscul. Disord. 12 (5): 506–12. PMID 12031626. 
  • 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. 
  • Mancuso M, Filosto M, Stevens JC, et al. (2003). "Mitochondrial myopathy and complex III deficiency in a patient with a new stop-codon mutation (G339X) in the cytochrome b gene.". J. Neurol. Sci. 209 (1-2): 61–3. PMID 12686403. 
  • 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. 
  • Kong QP, Yao YG, Liu M, et al. (2003). "Mitochondrial DNA sequence polymorphisms of five ethnic populations from northern China.". Hum. Genet. 113 (5): 391–405. doi:10.1007/s00439-003-1004-7. PMID 12938036. 
  • 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. 
  • Haut S, de Villemeur TB, Brivet M, et al. (2004). "The deleterious G15498A mutation in mitochondrial DNA-encoded cytochrome b may remain clinically silent in homoplasmic carriers.". Eur. J. Hum. Genet. 12 (3): 220–4. doi:10.1038/sj.ejhg.5201132. PMID 14735157. 
  • 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. 
  • Thangaraj K, Chaubey G, Kivisild T, et al. (2005). "Reconstructing the origin of Andaman Islanders.". Science 308 (5724): 996. doi:10.1126/science.1109987. PMID 15890876. 
  • Blakely EL, Mitchell AL, Fisher N, et al. (2005). "A mitochondrial cytochrome b mutation causing severe respiratory chain enzyme deficiency in humans and yeast.". FEBS J. 272 (14): 3583–92. doi:10.1111/j.1742-4658.2005.04779.x. PMID 16008558. 
  • Kivisild T, Shen P, Wall DP, et al. (2006). "The role of selection in the evolution of human mitochondrial genomes.". Genetics 172 (1): 373–87. doi:10.1534/genetics.105.043901. PMID 16172508. 
  • Behar DM, Metspalu E, Kivisild T, et al. (2006). "The matrilineal ancestry of Ashkenazi Jewry: portrait of a recent founder event.". Am. J. Hum. Genet. 78 (3): 487–97. doi:10.1086/500307. PMID 16404693. 
  • van Holst Pellekaan SM, Ingman M, Roberts-Thomson J, Harding RM (2006). "Mitochondrial genomics identifies major haplogroups in Aboriginal Australians.". Am. J. Phys. Anthropol. 131 (2): 282–94. doi:10.1002/ajpa.20426. PMID 16596590. 
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