| P705 | Ensembl protein ID | ENSMUSP00000034896 |
| ENSMUSP00000121424 | ||
| ENSMUSP00000123414 | ||
| P637 | RefSeq protein ID | NP_080934 |
| P352 | UniProt protein ID | Q923Z3 |
| P682 | biological process | tRNA processing | Q14914388 |
| tRNA methylation | Q21108966 | ||
| tRNA wobble uridine modification | Q21109964 | ||
| mitochondrial tRNA wobble uridine modification | Q21122422 | ||
| P681 | cell component | mitochondrion | Q39572 |
| P702 | encoded by | Mto1 | Q18263117 |
| P703 | found in taxon | house mouse | Q83310 |
| P527 | has part(s) | MnmG-related, conserved site | Q24766993 |
| GidA associated domain 3 | Q24788057 | ||
| P680 | molecular function | flavin adenine dinucleotide binding | Q14599303 |
| P361 | part of | tRNA uridine 5-carboxymethylaminomethyl modification enzyme MnmG | Q24722820 |
| FAD/NAD(P)-binding domain superfamily | Q41797313 | ||
| GidA associated domain 3, protein family | Q83166613 | ||
| MnmG-related, conserved site, protein family | Q95354340 |
| Q28512463 | Identification and characterization of mouse MTO1 gene related to mitochondrial tRNA modification |
| Q28217558 | Isolation and characterization of the putative nuclear modifier gene MTO1 involved in the pathogenesis of deafness-associated mitochondrial 12 S rRNA A1555G mutation |
| Q18263117 | Mto1 | encodes | P688 |
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