MT-TS1 Chromosome MT

Mitochondrially encoded tRNA-Ser (UCN) 1
6 variants 6 Health Risk

Upload your DNA to see your personal genotypes for variants in MT-TS1.

What This Gene Does
Predicted to enable triplet codon-amino acid adaptor activity. Predicted to be involved in translation. [provided by Alliance of Genome Resources, Jul 2025]
Gene Info
Gene Group
Mitochondrially encoded transfer RNAs
Locus Type
RNA, transfer
Location
mitochondria
Ensembl
ENSG00000210151
Associated Conditions (18)
MERRF/MELAS overlap syndrome
Mitochondrial cytochrome c oxidase deficiency
MELAS syndrome
Mitochondrial complex IV deficiency
nuclear type 1
Mitochondrial disease
Limb ataxia
Mitochondrial non-syndromic sensorineural hearing loss
neonatal lactic acidosis
Exercise intolerance
muscle pain
and lactic acidemia
Primary mitochondrial disorders
Deafness
sensorineural
with neurologic features
Rare genetic deafness
MERRF syndrome
Key Variants
All Variants (6)
RSID Category Clinical Significance Conditions
RS199474817 Health Risk Likely pathogenic MERRF/MELAS overlap syndrome, Mitochondrial cytochrome c oxidase deficiency, MELAS syndrome
RS199474820 Health Risk Likely pathogenic Mitochondrial non-syndromic sensorineural hearing loss, Mitochondrial disease, Mitochondrial non-syndromic sensorineural hearing loss
RS199474821 Health Risk Likely pathogenic Mitochondrial non-syndromic sensorineural hearing loss, MELAS syndrome, Mitochondrial complex IV deficiency
RS2068703521 Health Risk Likely pathogenic neonatal lactic acidosis, Mitochondrial complex IV deficiency, nuclear type 1
RS387906419 Health Risk Likely pathogenic Exercise intolerance, muscle pain, and lactic acidemia
RS111033319 Health Risk Pathogenic Mitochondrial cytochrome c oxidase deficiency, Deafness, sensorineural
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