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1 to 19 of 19  Show
  1. 1
    "Identification and characterization of two novel human mitochondrial elongation factor genes, hEFG2 and hEFG1, phylogenetically conserved through evolution."
    Hammarsund M., Wilson W., Corcoran M., Merup M., Einhorn S., Grander D., Sangfelt O.
    Hum. Genet. 109:542-550(2001) [PubMed] [Europe PMC] [Abstract]
    Cited for: NUCLEOTIDE SEQUENCE [MRNA] (ISOFORM 1), TISSUE SPECIFICITY.
    Category: Expression, Sequences.
    Source: UniProtKB/Swiss-Prot (reviewed).

    This publication is cited by 1 other entry.

  2. 2
    "Cloning of elongation factor G isoform."
    Zheng M., Xie Y., Mao Y.
    Submitted (OCT-2003) to the EMBL/GenBank/DDBJ databases
    Cited for: NUCLEOTIDE SEQUENCE [MRNA] (ISOFORM 4).
    Category: Sequences.
    Source: UniProtKB/Swiss-Prot (reviewed).
  3. 3
    "Complete sequencing and characterization of 21,243 full-length human cDNAs."
    Ota T., Suzuki Y., Nishikawa T., Otsuki T., Sugiyama T., Irie R., Wakamatsu A., Hayashi K., Sato H., Nagai K., Kimura K., Makita H., Sekine M., Obayashi M., Nishi T., Shibahara T., Tanaka T., Ishii S.
    Sugano S.
    Nat. Genet. 36:40-45(2004) [PubMed] [Europe PMC] [Abstract]
    Cited for: NUCLEOTIDE SEQUENCE [LARGE SCALE MRNA] (ISOFORM 5).
    Category: Sequences.
    Tissue: Colon.
    Source: UniProtKB/Swiss-Prot (reviewed).

    This publication is cited by 12927 other entries.

  4. 4
    Cited for: NUCLEOTIDE SEQUENCE [LARGE SCALE MRNA] (ISOFORM 2).
    Category: Sequences.
    Tissue: Aorta.
    Source: UniProtKB/Swiss-Prot (reviewed).
  5. 5
    Category: Sequences.
    Source: UniProtKB/Swiss-Prot (reviewed).
  6. 6
    "The status, quality, and expansion of the NIH full-length cDNA project: the Mammalian Gene Collection (MGC)."
    The MGC Project Team
    Genome Res. 14:2121-2127(2004) [PubMed] [Europe PMC] [Abstract]
    Cited for: NUCLEOTIDE SEQUENCE [LARGE SCALE MRNA] (ISOFORMS 1 AND 3), VARIANTS HIS-425; GLY-594 AND GLY-735.
    Category: Sequences.
    Tissue: Brain and Skin.
    Source: UniProtKB/Swiss-Prot (reviewed).

    This publication is cited by 50448 other entries.

  7. 7
    "EF-G2mt is an exclusive recycling factor in mammalian mitochondrial protein synthesis."
    Tsuboi M., Morita H., Nozaki Y., Akama K., Ueda T., Ito K., Nierhaus K.H., Takeuchi N.
    Mol. Cell 35:502-510(2009) [PubMed] [Europe PMC] [Abstract]
    Cited for: FUNCTION.
    Category: Function.
    Source: UniProtKB/Swiss-Prot (reviewed).

    This publication is cited by 1 and mapped to 88 other entries.

  8. 8
    Cited for: IDENTIFICATION BY MASS SPECTROMETRY [LARGE SCALE ANALYSIS].
    Category: Sequences.
    Source: UniProtKB/Swiss-Prot (reviewed).

    This publication is cited by 18117 other entries.

  9. 9
    "An enzyme assisted RP-RPLC approach for in-depth analysis of human liver phosphoproteome."
    Bian Y., Song C., Cheng K., Dong M., Wang F., Huang J., Sun D., Wang L., Ye M., Zou H.
    J. Proteomics 96:253-262(2014) [PubMed] [Europe PMC] [Abstract]
    Cited for: IDENTIFICATION BY MASS SPECTROMETRY [LARGE SCALE ANALYSIS].
    Category: Sequences.
    Tissue: Liver.
    Source: UniProtKB/Swiss-Prot (reviewed).

    This publication is cited by 11551 other entries.

  10. 10
    "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. 60:509-513(2015) [PubMed] [Europe PMC] [Abstract]
    Cited for: INVOLVEMENT IN COXPD39.
    Category: Pathology & Biotech.
    Source: UniProtKB/Swiss-Prot (reviewed).

    This publication is mapped to 1 other entry.

  11. 11
    Category: Pathology & Biotech, Sequences.
    Source: UniProtKB/Swiss-Prot (reviewed).

    This publication is cited by 1 other entry.

  12. 12
    "Novel GFM2 variants associated with early-onset neurological presentations of mitochondrial disease and impaired expression of OXPHOS subunits."
    Glasgow R.I.C., Thompson K., Barbosa I.A., He L., Alston C.L., Deshpande C., Simpson M.A., Morris A.A.M., Neu A., Loebel U., Hall J., Prokisch H., Haack T.B., Hempel M., McFarland R., Taylor R.W.
    Neurogenetics 18:227-235(2017) [PubMed] [Europe PMC] [Abstract]
    Cited for: VARIANTS COXPD39 SER-92 AND GLN-190, INVOLVEMENT IN COXPD39.
    Category: Pathology & Biotech, Sequences.
    Source: UniProtKB/Swiss-Prot (reviewed).
  13. 13
    "The A3243G tRNALeu(UUR) MELAS mutation causes amino acid misincorporation and a combined respiratory chain assembly defect partially suppressed by overexpression of EFTu and EFG2."
    Sasarman F., Antonicka H., Shoubridge E.A.
    Hum. Mol. Genet. 17:3697-3707(2008) [PubMed] [Europe PMC] [Abstract]
    Category: Pathology & Biotech.
    Annotation: Myoblasts isolated from the MELAS patients show A3243G mutation in tRNALeu(UUR) produces a severe respiratory chain deficiency and this phenotype can be partially suppressed by overexpression of EFTu and EFG2.
    Source: GeneRIF:84340.

    This publication is mapped to 4 other entries.

  14. 14
    "Mammalian BTBD12/SLX4 assembles a Holliday junction resolvase and is required for DNA repair."
    Svendsen J.M., Smogorzewska A., Sowa M.E., O'Connell B.C., Gygi S.P., Elledge S.J., Harper J.W.
    Cell 138:63-77(2009) [PubMed] [Europe PMC] [Abstract]
    Category: Interaction.
    Source: IntAct:Q969S9.

    This publication is cited by 8 and mapped to 206 other entries.

  15. 15
    "A comprehensive resource of interacting protein regions for refining human transcription factor networks."
    Miyamoto-Sato E., Fujimori S., Ishizaka M., Hirai N., Masuoka K., Saito R., Ozawa Y., Hino K., Washio T., Tomita M., Yamashita T., Oshikubo T., Akasaka H., Sugiyama J., Matsumoto Y., Yanagawa H.
    PLoS ONE 5:e9289-e9289(2010) [PubMed] [Europe PMC] [Abstract]
    Category: Interaction.
    Source: IntAct:Q969S9.

    This publication is mapped to 720 other entries.

  16. 16
    Category: Function.
    Annotation: Observational study of gene-disease association. (HuGE Navigator).
    Source: GeneRIF:84340.

    This publication is mapped to 3063 other entries.

  17. 17
    "Polymorphisms in the mitochondrial ribosome recycling factor EF-G2mt/MEF2 compromise cell respiratory function and increase atorvastatin toxicity."
    Callegari S., Gregory P.A., Sykes M.J., Bellon J., Andrews S., McKinnon R.A., de Barros Lopes M.A.
    PLoS Genet. 8:e1002755-e1002755(2012) [PubMed] [Europe PMC] [Abstract]
    Category: Function, Pathology & Biotech.
    Annotation: These findings constitute the first reported phenotype associated with SNPs in the EF-G2mt gene and implicate the human EF-G2mt gene as a pharmacogenetic candidate gene for statin toxicity in humans.
    Source: GeneRIF:84340.

    This publication is mapped to 3 other entries.

  18. 18
    Category: Interaction.
    Source: IntAct:Q969S9.

    This publication is mapped to 4105 other entries.

  19. 19
    "Proteomic analyses reveal distinct chromatin-associated and soluble transcription factor complexes."
    Li X., Wang W., Wang J., Malovannaya A., Xi Y., Li W., Guerra R., Hawke D.H., Qin J., Chen J.
    Mol. Syst. Biol. 11:775-775(2015) [PubMed] [Europe PMC] [Abstract]
    Category: Interaction.
    Source: IntAct:Q969S9.

    This publication is mapped to 1979 other entries.

1 to 19 of 19  Show
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