tRNA (guanine(37)-N1)-methyltransferase isoform 3 [Homo sapiens]

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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 mRNA
See reference mRNA sequence for the TRMT5 gene (NM_020810.3).
RefSeq protein isoforms
See 3 reference sequence protein isoforms for the TRMT5 gene.

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NP_065861 [Domain Mapping of Disease Mut...]
NP_065861
Domain Mapping of Disease Mutations
Ensembl [Ensembl]
Ensembl
GlyGen glycoinformatics resource [GlyGen glycoinformatics resou...]
GlyGen glycoinformatics resource
Transcript/Protein Information [PANTHER Classification System]
Transcript/Protein Information
PANTHER Classification System
reagents [ExactAntigen/Labome]
reagents
ExactAntigen/Labome

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Protein