RecName: Full=tRNA (guanine(37)-N1)-methyltransferase; AltName: Full=M - Protein

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A novel TRMT5 mutation causes a complex inherited neuropathy syndrome: The role of nerve pathology in defining a demyelinating neuropathy. [Neuropathol Appl Neurobiol. 2022]
A novel TRMT5 mutation causes a complex inherited neuropathy syndrome: The role of nerve pathology in defining a demyelinating neuropathy.
Argente-Escrig H, Vílchez JJ, Frasquet M, Muelas N, Azorín I, Vílchez R, Millet-Sancho E, Pitarch I, Tomás-Vila M, Vázquez-Costa JF, et al. Neuropathol Appl Neurobiol. 2022 Aug; 48(5):e12817. Epub 2022 Apr 10.
TRMT5 mutations are associated with features of complex hereditary spastic paraparesis. [Neurology. 2017]
TRMT5 mutations are associated with features of complex hereditary spastic paraparesis.
Tarnopolsky MA, Brady L, Tetreault M, Care4Rare Canada Consortium. Neurology. 2017 Nov 21; 89(21):2210-2211. Epub 2017 Oct 11.
Conservation of structure and mechanism by Trm5 enzymes. [RNA. 2013]
Conservation of structure and mechanism by Trm5 enzymes.
Christian T, Gamper H, Hou YM. RNA. 2013 Sep; 19(9):1192-9. Epub 2013 Jul 25.

RefSeq genomic sequence
See the genomic reference sequence for the TRMT5 gene (NG_053119.1).
RefSeq protein isoforms
See 3 reference sequence protein isoforms for the TRMT5 gene.

Q32P41 [Domain Mapping of Disease Mut...]
Q32P41
Domain Mapping of Disease Mutations
Reactome [Reactome]
Reactome

RecName: Full=tRNA (guanine(37)-N1)-methyltransferase; AltName: Full=M1G-methylt...
RecName: Full=tRNA (guanine(37)-N1)-methyltransferase; AltName: Full=M1G-methyltransferase; AltName: Full=tRNA [GM37] methyltransferase; AltName: Full=tRNA methyltransferase 5 homolog
gi|2528974266|sp|Q32P41.3|TRM5_HUMA

Protein
Homo sapiens cDNA FLJ32056 fis, clone NTONG2001619
Homo sapiens cDNA FLJ32056 fis, clone NTONG2001619
gi|16552070|dbj|AK056618.1|

Nucleotide

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Protein