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Search Thermo Fisher Scientific
Immunogen sequence: GITINAAHV EYSTAARHYA HTDCPGHADY VKNMITGTAP LDGCILVVAA NDGPMPQTRE HLLLARQIGV EHVVVYVNKA DAVQDSEMVE LVELEIRELL TEFGYKGEET PVIVGSALCA LEGRDPELGL KSVQKLLDAV DTYIPVPARD LEKPFLLPVE AVYSVPGRGT VVTGTLERGI LKKGDECELL GHSKNIRTVV TGIEMFHKSL ERAEAGDNLG ALVRGLKRED LRRGLVMVKP GSIKPHQKVE AQVYILSKEE GGRHKPFVSH FMPVMFSLTW DMACRIILPP EKELAMPGED LKFNLILRQP MILEKGQRFT LRDGNRTIGT GLVTNTLAMT EEEKNIKWG (108-455 aa encoded by BC010041)
This gene encodes a protein which participates in protein translation in mitochondria. Mutations in this gene have been associated with combined oxidative phosphorylation deficiency resulting in lactic acidosis and fatal encephalopathy. A pseudogene has been identified on chromosome 17.
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Protein Aliases: EF-Tu; Elongation factor Tu, mitochondrial; P43; tufm {ECO:0000250|UniProtKB:P49411}
Gene Aliases: 2300002G02Rik; C76308; C76389; COXPD4; EF-TuMT; EFTU; P43; TUFM
UniProt ID: (Human) P49411, (Mouse) Q8BFR5, (Rat) P85834
Entrez Gene ID: (Human) 7284, (Mouse) 233870, (Rat) 293481
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