TRMU Chromosome 22

TRNA mitochondrial 2-thiouridylase
167 variants 167 Health Risk

Upload your DNA to see your personal genotypes for variants in TRMU.

What This Gene Does
This nuclear gene encodes a mitochondrial tRNA-modifying enzyme. The encoded protein catalyzes the 2-thiolation of uridine on the wobble positions of tRNA(Lys), tRNA(Glu), and tRNA(Gln), resulting in the formation of 5-taurinomethyl-2-thiouridine moieties. Mutations in this gene may cause transient infantile liver failure. Polymorphisms in this gene may also influence the severity of deafness caused by mitochondrial 12S ribosomal RNA mutations. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Sep 2013]
Associated Conditions (6)
Acute infantile liver failure due to synthesis defect of mtDNA-encoded proteins
Inborn genetic diseases
TRMU-related disorder
Aminoglycoside-induced deafness
Germ cell tumor of testis
Lung cancer
Key Variants
RS1006261196
Conflicting classifications of pathogenicity
Health Risk
RS111608902
Conflicting classifications of pathogenicity
Acute infantile liver failure due to synthesis defect of mtDNA-encoded proteins, Inborn genetic diseases, Acute infantile liver failure due to synthesis defect of mtDNA-encoded proteins
Health Risk
RS113846383
Conflicting classifications of pathogenicity
Acute infantile liver failure due to synthesis defect of mtDNA-encoded proteins, Acute infantile liver failure due to synthesis defect of mtDNA-encoded proteins
Health Risk
RS117710834
Conflicting classifications of pathogenicity
Acute infantile liver failure due to synthesis defect of mtDNA-encoded proteins, Acute infantile liver failure due to synthesis defect of mtDNA-encoded proteins
Health Risk
RS1294405938
Conflicting classifications of pathogenicity
TRMU-related disorder, TRMU-related disorder
Health Risk
RS138586787
Conflicting classifications of pathogenicity
Acute infantile liver failure due to synthesis defect of mtDNA-encoded proteins, Acute infantile liver failure due to synthesis defect of mtDNA-encoded proteins
Health Risk
RS139351059
Conflicting classifications of pathogenicity
Health Risk
RS142346622
Conflicting classifications of pathogenicity
Acute infantile liver failure due to synthesis defect of mtDNA-encoded proteins, Acute infantile liver failure due to synthesis defect of mtDNA-encoded proteins
Health Risk
RS1426898716
Conflicting classifications of pathogenicity
Health Risk
RS144054758
Conflicting classifications of pathogenicity
Acute infantile liver failure due to synthesis defect of mtDNA-encoded proteins, TRMU-related disorder, Inborn genetic diseases
Health Risk
RS1440658479
Conflicting classifications of pathogenicity
Acute infantile liver failure due to synthesis defect of mtDNA-encoded proteins, Acute infantile liver failure due to synthesis defect of mtDNA-encoded proteins
Health Risk
RS147754663
Conflicting classifications of pathogenicity
Acute infantile liver failure due to synthesis defect of mtDNA-encoded proteins, TRMU-related disorder, Inborn genetic diseases
Health Risk
All Variants (167)
RSID Category Clinical Significance Conditions
RS779868712 Health Risk Likely pathogenic Aminoglycoside-induced deafness, Acute infantile liver failure due to synthesis defect of mtDNA-encoded proteins, Aminoglycoside-induced deafness
RS863224239 Health Risk Likely pathogenic
RS914793719 Health Risk Likely pathogenic Aminoglycoside-induced deafness, Aminoglycoside-induced deafness
RS926748713 Health Risk Likely pathogenic Inborn genetic diseases, Inborn genetic diseases
RS1174791046 Health Risk Pathogenic Acute infantile liver failure due to synthesis defect of mtDNA-encoded proteins, Aminoglycoside-induced deafness, Acute infantile liver failure due to synthesis defect of mtDNA-encoded proteins
RS118203990 Health Risk Pathogenic Acute infantile liver failure due to synthesis defect of mtDNA-encoded proteins, Aminoglycoside-induced deafness, TRMU-related disorder
RS118203991 Health Risk Pathogenic Acute infantile liver failure due to synthesis defect of mtDNA-encoded proteins, Acute infantile liver failure due to synthesis defect of mtDNA-encoded proteins
RS1225948299 Health Risk Pathogenic Acute infantile liver failure due to synthesis defect of mtDNA-encoded proteins, Aminoglycoside-induced deafness, Acute infantile liver failure due to synthesis defect of mtDNA-encoded proteins
RS1226116719 Health Risk Pathogenic
RS1275469562 Health Risk Pathogenic
RS1297282365 Health Risk Pathogenic Lung cancer, Lung cancer
RS1372867653 Health Risk Pathogenic
RS1441183063 Health Risk Pathogenic
RS1447532733 Health Risk Pathogenic
RS1490906786 Health Risk Pathogenic Acute infantile liver failure due to synthesis defect of mtDNA-encoded proteins, Aminoglycoside-induced deafness, Acute infantile liver failure due to synthesis defect of mtDNA-encoded proteins
RS1601968978 Health Risk Pathogenic
RS2077957264 Health Risk Pathogenic
RS2077957664 Health Risk Pathogenic
RS2078260891 Health Risk Pathogenic
RS2078261207 Health Risk Pathogenic Aminoglycoside-induced deafness, Aminoglycoside-induced deafness
RS2078377046 Health Risk Pathogenic
RS2078575287 Health Risk Pathogenic
RS2147081045 Health Risk Pathogenic
RS2147095810 Health Risk Pathogenic
RS2147095916 Health Risk Pathogenic
RS2147113826 Health Risk Pathogenic
RS2518132021 Health Risk Pathogenic
RS2518150291 Health Risk Pathogenic
RS2518178649 Health Risk Pathogenic
RS2518179076 Health Risk Pathogenic
RS2518179292 Health Risk Pathogenic
RS2518179937 Health Risk Pathogenic
RS2518190941 Health Risk Pathogenic
RS2518191775 Health Risk Pathogenic
RS2518201657 Health Risk Pathogenic
RS2518211131 Health Risk Pathogenic
RS2518211177 Health Risk Pathogenic
RS2518211384 Health Risk Pathogenic
RS2518211396 Health Risk Pathogenic
RS2518211501 Health Risk Pathogenic
RS2518211598 Health Risk Pathogenic
RS2518216310 Health Risk Pathogenic
RS367683258 Health Risk Pathogenic Acute infantile liver failure due to synthesis defect of mtDNA-encoded proteins, Aminoglycoside-induced deafness, Acute infantile liver failure due to synthesis defect of mtDNA-encoded proteins
RS387907022 Health Risk Pathogenic Acute infantile liver failure due to synthesis defect of mtDNA-encoded proteins, Inborn genetic diseases, Aminoglycoside-induced deafness
RS778799889 Health Risk Pathogenic Acute infantile liver failure due to synthesis defect of mtDNA-encoded proteins, Acute infantile liver failure due to synthesis defect of mtDNA-encoded proteins
RS118203992 Health Risk Pathogenic/Likely pathogenic Acute infantile liver failure due to synthesis defect of mtDNA-encoded proteins, Acute infantile liver failure due to synthesis defect of mtDNA-encoded proteins, Aminoglycoside-induced deafness
RS1206163048 Health Risk Pathogenic/Likely pathogenic
RS1436976326 Health Risk Pathogenic/Likely pathogenic Aminoglycoside-induced deafness, Aminoglycoside-induced deafness
RS1464059546 Health Risk Pathogenic/Likely pathogenic Aminoglycoside-induced deafness, Aminoglycoside-induced deafness
RS1800386420 Health Risk Pathogenic/Likely pathogenic Aminoglycoside-induced deafness, Aminoglycoside-induced deafness
Sign Up to Analyze Your DNA Log In