elongation factor G2 [Homo sapiens]

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Novel GFM2 variants associated with early-onset neurological presentations of mitochondrial disease and impaired expression of OXPHOS subunits. [Neurogenetics. 2017]
Novel GFM2 variants associated with early-onset neurological presentations of mitochondrial disease and impaired expression of OXPHOS subunits.
Glasgow RIC, Thompson K, Barbosa IA, He L, Alston CL, Deshpande C, Simpson MA, Morris AAM, Neu A, Löbel U, et al. Neurogenetics. 2017 Dec; 18(4):227-235. Epub 2017 Oct 26.
Compound heterozygous GFM2 mutations with Leigh syndrome complicated by arthrogryposis multiplex congenita. [J Hum Genet. 2015]
Compound heterozygous GFM2 mutations with Leigh syndrome complicated by arthrogryposis multiplex congenita.
Fukumura S, Ohba C, Watanabe T, Minagawa K, Shimura M, Murayama K, Ohtake A, Saitsu H, Matsumoto N, Tsutsumi H. J Hum Genet. 2015 Sep; 60(9):509-13. Epub 2015 May 28.
Polymorphisms in the mitochondrial ribosome recycling factor EF-G2mt/MEF2 compromise cell respiratory function and increase atorvastatin toxicity. [PLoS Genet. 2012]
Polymorphisms in the mitochondrial ribosome recycling factor EF-G2mt/MEF2 compromise cell respiratory function and increase atorvastatin toxicity.
Callegari S, Gregory PA, Sykes MJ, Bellon J, Andrews S, McKinnon RA, de Barros Lopes MA. PLoS Genet. 2012; 8(6):e1002755. Epub 2012 Jun 14.

RefSeq genomic sequence
See the genomic reference sequence for the GFM2 gene (NG_011531.1).
RefSeq protein isoforms
See 14 reference sequence protein isoforms for the GFM2 gene.

Nucleotide
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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)
reagents [ExactAntigen/Labome]
reagents
ExactAntigen/Labome

cytochrome c oxidase subunit I, partial (mitochondrion) [Trichinella spiralis]
cytochrome c oxidase subunit I, partial (mitochondrion) [Trichinella spiralis]
gi|1734264401|gb|QEL52068.1|

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Protein