The TRMU gene homepage

General information
Gene symbol TRMU
Gene name tRNA 5-methylaminomethyl-2-thiouridylate methyltransferase
Chromosome 22
Chromosomal band q13
Imprinted Unknown
Genomic reference NG_012173.1
Transcript reference NM_018006.4
Exon/intron information NM_018006.4 exon/intron table
Associated with diseases LFIT, deafness, aminoglycoside-induced
Citation reference(s) -
Refseq URL Genomic reference sequence
Curators (1) Global Variome, with Curator vacancy
Total number of public variants reported 23
Unique public DNA variants reported 19
Individuals with public variants 303
Hidden variants -
Download all this gene's data Download all data
Notes Establishment of the database was supported by the European Community's Seventh Framework Programme (FP7/2007-2013) under grant agreement No 200754 - the GEN2PHEN project.
Date created April 29, 2010
Date last updated November 01, 2022
Version TRMU:221101

Graphical displays and utilities
Graphs Graphs displaying summary information of all variants in the database »
Reading frame checker The Reading-frame checker generates a prediction of the effect of whole-exon changes. Active for: NM_018006.4.
UCSC Genome Browser Show variants in the UCSC Genome Browser (full view, compact view)
Ensembl Genome Browser Show variants in the Ensembl Genome Browser (full view, compact view)
NCBI Sequence Viewer Show distribution histogram of variants in the NCBI Sequence Viewer

Links to other resources
Homepage URL https://www.LOVD.nl/TRMU
HGNC 25481
Entrez Gene 55687
PubMed articles TRMU
OMIM - Gene 610230
OMIM - Diseases LFIT (failure, liver, transient, infantile (LFIT))
deafness, aminoglycoside-induced
HGMD TRMU
GeneCards TRMU
GeneTests TRMU
Orphanet TRMU


Active transcripts


ID     

Chr     

Name     

NCBI ID     

NCBI Protein ID     

DescendingVariants     
00021890 22 transcript variant 1 NM_018006.4 NP_060476.2 23


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