MTO1

MTO1
Identifiers
AliasesMTO1, COXPD10, CGI-02, mitochondrial tRNA translation optimization 1
External IDsMGI: 1915541 HomoloGene: 5876 GeneCards: MTO1
Gene location (Human)
Chr.Chromosome 6 (human)[1]
Band6q13Start73,461,578 bp[1]
End73,509,236 bp[1]
Orthologs
SpeciesHumanMouse
Entrez

25821

68291

Ensembl

ENSG00000135297

ENSMUSG00000032342

UniProt

Q9Y2Z2

Q923Z3

RefSeq (mRNA)

NM_001123226
NM_012123
NM_133645

NM_026658

RefSeq (protein)

NP_001116698
NP_036255
NP_598400

NP_080934

Location (UCSC)Chr 6: 73.46 – 73.51 MbChr 9: 78.45 – 78.48 Mb
PubMed search[3][4]
Wikidata
View/Edit HumanView/Edit Mouse

Protein MTO1 homolog, mitochondrial is a protein that in humans is encoded by the MTO1 gene.[5][6]

References

  1. 1 2 3 GRCh38: Ensembl release 89: ENSG00000135297 - Ensembl, May 2017
  2. 1 2 3 GRCm38: Ensembl release 89: ENSMUSG00000032342 - Ensembl, May 2017
  3. ↑ "Human PubMed Reference:".
  4. ↑ "Mouse PubMed Reference:".
  5. ↑ Li X, Li R, Lin X, Guan MX (Jul 2002). "Isolation and characterization of the putative nuclear modifier gene MTO1 involved in the pathogenesis of deafness-associated mitochondrial 12 S rRNA A1555G mutation". J Biol Chem. 277 (30): 27256–64. doi:10.1074/jbc.M203267200. PMID 12011058.
  6. ↑ "Entrez Gene: MTO1 mitochondrial translation optimization 1 homolog (S. cerevisiae)".

Further reading

  • Maruyama K, Sugano S (1994). "Oligo-capping: a simple method to replace the cap structure of eukaryotic mRNAs with oligoribonucleotides". Gene. 138 (1–2): 171–4. doi:10.1016/0378-1119(94)90802-8. PMID 8125298.
  • Suzuki Y, Yoshitomo-Nakagawa K, Maruyama K, et al. (1997). "Construction and characterization of a full length-enriched and a 5'-end-enriched cDNA library". Gene. 200 (1–2): 149–56. doi:10.1016/S0378-1119(97)00411-3. PMID 9373149.
  • Lai CH, Chou CY, Ch'ang LY, et al. (2000). "Identification of novel human genes evolutionarily conserved in Caenorhabditis elegans by comparative proteomics". Genome Res. 10 (5): 703–13. doi:10.1101/gr.10.5.703. PMC 310876. PMID 10810093.
  • Strausberg RL, Feingold EA, Grouse LH, et al. (2003). "Generation and initial analysis of more than 15,000 full-length human and mouse cDNA sequences". Proc. Natl. Acad. Sci. U.S.A. 99 (26): 16899–903. doi:10.1073/pnas.242603899. PMC 139241. PMID 12477932.
  • Mungall AJ, Palmer SA, Sims SK, et al. (2003). "The DNA sequence and analysis of human chromosome 6". Nature. 425 (6960): 805–11. doi:10.1038/nature02055. PMID 14574404.
  • Gerhard DS, Wagner L, Feingold EA, et al. (2004). "The status, quality, and expansion of the NIH full-length cDNA project: the Mammalian Gene Collection (MGC)". Genome Res. 14 (10B): 2121–7. doi:10.1101/gr.2596504. PMC 528928. PMID 15489334.
  • Bykhovskaya Y, Mengesha E, Wang D, et al. (2005). "Phenotype of non-syndromic deafness associated with the mitochondrial A1555G mutation is modulated by mitochondrial RNA modifying enzymes MTO1 and GTPBP3". Mol. Genet. Metab. 83 (3): 199–206. doi:10.1016/j.ymgme.2004.07.009. PMID 15542390.
  • Krull M, Brosius J, Schmitz J (2005). "Alu-SINE exonization: en route to protein-coding function". Mol. Biol. Evol. 22 (8): 1702–11. doi:10.1093/molbev/msi164. PMID 15901843.


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