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MTO1

From Wikipedia, the free encyclopedia
MTO1
Identifiers
AliasesMTO1, COXPD10, CGI-02, mitochondrial tRNA translation optimization 1
External IDsOMIM: 614667; MGI: 1915541; HomoloGene: 5876; GeneCards: MTO1; OMA:MTO1 - orthologs
Orthologs
SpeciesHumanMouse
Entrez
Ensembl
UniProt
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: 78.36 – 78.38 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

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  1. ^ a b c GRCh38: Ensembl release 89: ENSG00000135297Ensembl, May 2017
  2. ^ a b c GRCm38: Ensembl release 89: ENSMUSG00000032342Ensembl, May 2017
  3. ^ "Human PubMed Reference:". National Center for Biotechnology Information, U.S. National Library of Medicine.
  4. ^ "Mouse PubMed Reference:". National Center for Biotechnology Information, U.S. National Library of Medicine.
  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

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