CYTB

Cytochrome b
Identifiers
Symbols	CYTB ; MTCYB
External IDs	Template:MGI HomoloGene: 5013
Gene ontology
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 b, also known as CYTB, is a human gene.

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.CS1 maint: Multiple names: authors list (link)
• Maca-Meyer N, González AM, Larruga JM; et al. (2003). "Major genomic mitochondrial lineages delineate early human expansions". BMC Genet. 2: 13. PMID 11553319.CS1 maint: Explicit use of et al. (link) CS1 maint: Multiple names: authors list (link)
• 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.CS1 maint: Explicit use of et al. (link) CS1 maint: Multiple names: authors list (link)
• 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.CS1 maint: Explicit use of et al. (link) CS1 maint: Multiple names: authors list (link)
• 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.CS1 maint: Explicit use of et al. (link) CS1 maint: Multiple names: authors list (link)
• 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.CS1 maint: Explicit use of et al. (link) CS1 maint: Multiple names: authors list (link)
• 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.CS1 maint: Explicit use of et al. (link) CS1 maint: Multiple names: authors list (link)
• 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.CS1 maint: Explicit use of et al. (link) CS1 maint: Multiple names: authors list (link)
• 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.CS1 maint: Explicit use of et al. (link) CS1 maint: Multiple names: authors list (link)
• 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.CS1 maint: Explicit use of et al. (link) CS1 maint: Multiple names: authors list (link)
• 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.CS1 maint: Explicit use of et al. (link) CS1 maint: Multiple names: authors list (link)
• 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.CS1 maint: Explicit use of et al. (link) CS1 maint: Multiple names: authors list (link)
• 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.CS1 maint: Explicit use of et al. (link) CS1 maint: Multiple names: authors list (link)
• 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.CS1 maint: Explicit use of et al. (link) CS1 maint: Multiple names: authors list (link)
• 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.CS1 maint: Explicit use of et al. (link) CS1 maint: Multiple names: authors list (link)
• 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.CS1 maint: Explicit use of et al. (link) CS1 maint: Multiple names: authors list (link)
• 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.CS1 maint: Explicit use of et al. (link) CS1 maint: Multiple names: authors list (link)
• 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.CS1 maint: Explicit use of et al. (link) CS1 maint: Multiple names: authors list (link)
• 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.CS1 maint: Multiple names: authors list (link)