unnamed protein product [Mus musculus]

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Disrupted mitochondrial function in the Opa3L122P mouse model for Costeff Syndrome impairs skeletal integrity. [Hum Mol Genet. 2016]
Disrupted mitochondrial function in the Opa3L122P mouse model for Costeff Syndrome impairs skeletal integrity.
Navein AE, Cooke EJ, Davies JR, Smith TG, Wells LH, Ohazama A, Healy C, Sharpe PT, Evans SL, Evans BA, et al. Hum Mol Genet. 2016 Jun 15; 25(12):2404-2416. Epub 2016 Apr 22.
Opa3, a novel regulator of mitochondrial function, controls thermogenesis and abdominal fat mass in a mouse model for Costeff syndrome. [Hum Mol Genet. 2012]
Opa3, a novel regulator of mitochondrial function, controls thermogenesis and abdominal fat mass in a mouse model for Costeff syndrome.
Wells T, Davies JR, Guschina IA, Ball DJ, Davies JS, Davies VJ, Evans BA, Votruba M. Hum Mol Genet. 2012 Nov 15; 21(22):4836-44. Epub 2012 Aug 6.
A missense mutation in the murine Opa3 gene models human Costeff syndrome. [Brain. 2008]
A missense mutation in the murine Opa3 gene models human Costeff syndrome.
Davies VJ, Powell KA, White KE, Yip W, Hogan V, Hollins AJ, Davies JR, Piechota M, Brownstein DG, Moat SJ, et al. Brain. 2008 Feb; 131(Pt 2):368-80.

RefSeq protein
See the reference protein sequence for optic atrophy 3 protein homolog (NP_997408.2).

Nucleotide
Nucleotide sequence from coding region
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Transcript/Protein Information [PANTHER Classification System]
Transcript/Protein Information
PANTHER Classification System
reagents [ExactAntigen/Labome]
reagents
ExactAntigen/Labome

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Protein