CSRP2BP [Homo sapiens]

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Mutated PET117 causes complex IV deficiency and is associated with neurodevelopmental regression and medulla oblongata lesions. [Hum Genet. 2017]
Mutated PET117 causes complex IV deficiency and is associated with neurodevelopmental regression and medulla oblongata lesions.
Renkema GH, Visser G, Baertling F, Wintjes LT, Wolters VM, van Montfrans J, de Kort GAP, Nikkels PGJ, van Hasselt PM, van der Crabben SN, et al. Hum Genet. 2017 Jun; 136(6):759-769. Epub 2017 Apr 6.
MR-1S Interacts with PET100 and PET117 in Module-Based Assembly of Human Cytochrome c Oxidase. [Cell Rep. 2017]
MR-1S Interacts with PET100 and PET117 in Module-Based Assembly of Human Cytochrome c Oxidase.
Vidoni S, Harbour ME, Guerrero-Castillo S, Signes A, Ding S, Fearnley IM, Taylor RW, Tiranti V, Arnold S, Fernandez-Vizarra E, et al. Cell Rep. 2017 Feb 14; 18(7):1727-1738.
The Assembly Factor Pet117 Couples Heme a Synthase Activity to Cytochrome Oxidase Assembly. [J Biol Chem. 2017]
The Assembly Factor Pet117 Couples Heme a Synthase Activity to Cytochrome Oxidase Assembly.
Taylor NG, Swenson S, Harris NJ, Germany EM, Fox JL, Khalimonchuk O. J Biol Chem. 2017 Feb 3; 292(5):1815-1825. Epub 2016 Dec 20.

RefSeq protein
See the reference protein sequence for protein PET117 homolog, mitochondrial precursor (NP_001158283.1).

Nucleotide
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CSRP2BP [Homo sapiens]
CSRP2BP [Homo sapiens]
gi|37182454|gb|AAQ89029.1|

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Protein