cytochrome c oxidase subunit VIb [Homo sapiens]

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Mitochondrial complex IV deficiency, caused by mutated COX6B1, is associated with encephalomyopathy, hydrocephalus and cardiomyopathy. [Eur J Hum Genet. 2015]
Mitochondrial complex IV deficiency, caused by mutated COX6B1, is associated with encephalomyopathy, hydrocephalus and cardiomyopathy.
Abdulhag UN, Soiferman D, Schueler-Furman O, Miller C, Shaag A, Elpeleg O, Edvardson S, Saada A. Eur J Hum Genet. 2015 Feb; 23(2):159-64. Epub 2014 Apr 30.
Severe infantile encephalomyopathy caused by a mutation in COX6B1, a nucleus-encoded subunit of cytochrome c oxidase. [Am J Hum Genet. 2008]
Severe infantile encephalomyopathy caused by a mutation in COX6B1, a nucleus-encoded subunit of cytochrome c oxidase.
Massa V, Fernandez-Vizarra E, Alshahwan S, Bakhsh E, Goffrini P, Ferrero I, Mereghetti P, D'Adamo P, Gasparini P, Zeviani M. Am J Hum Genet. 2008 Jun; 82(6):1281-9. Epub 2008 May 22.
Nucleotide sequence of cDNA encoding subunit VIb of human cytochrome c oxidase. [Nucleic Acids Res. 1989]
Nucleotide sequence of cDNA encoding subunit VIb of human cytochrome c oxidase.
Taanman JW, Schrage C, Ponne N, Bolhuis P, de Vries H, Agsteribbe E. Nucleic Acids Res. 1989 Feb 25; 17(4):1766.

RefSeq genomic sequence
See the genomic reference sequence for the COX6B1 gene (NG_012193.1).
RefSeq protein
See the reference protein sequence for cytochrome c oxidase subunit 6B1 (NP_001854.1).

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MODBASE, Database of Comparative Protein Structure Models (Sali Lab/UCSF) [MODBASE, Database of Comparat...]
MODBASE, Database of Comparative Protein Structure Models (Sali Lab/UCSF)
Transcript/Protein Information [PANTHER Classification System]
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PANTHER Classification System
reagents [ExactAntigen/Labome]
reagents
ExactAntigen/Labome
reagent reviews [ExactAntigen/Labome]
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ExactAntigen/Labome

cytochrome c oxidase subunit VIb [Homo sapiens]
cytochrome c oxidase subunit VIb [Homo sapiens]
gi|30582729|gb|AAP35591.1|

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