Gene
MT-TN
mitochondrially encoded tRNA-Asn (AAU/C)
- HGNC 7493↗(opens in a new tab)
- Ensembl gene ENSG00000210135↗(opens in a new tab)
- NCBI Gene 4570↗(opens in a new tab)
Summary
- Cytogenetic location
- mitochondria
- Also known as
- trnN
- Previous symbols
- MTTN
- Locus type
- RNA, transfer
Reference genomeGRCh38hg38
Positions on gene and variant pages follow this choice, in this browser.
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Traits linked to MT-TN
The Human Phenotype Ontology lists these as features of the rare conditions MT-TN can cause. Each trait's page lists the other genes linked to it.
Abnormality of the nervous system
- Ataxia
- Brisk reflexes
- Instability or lack of coordination of central trunk muscles
- Loss of developmental milestones
- Depression
- Intellectual disability, mild
- Epilepsy
- Global developmental delay
Show 3 more traits
Abnormality of the musculoskeletal system
- Cytochrome C oxidase-negative muscle fibers
- Generalized decreased muscle tone
- Low muscle tone
- Muscle abnormality related to mitochondrial dysfunction
- Axial muscle weakness
- Decreased lung function due to weak breathing muscles
- EMG abnormality
- Progressive proximal muscle weakness
Show 1 more trait
External links
Where this comes from
- HGNC: the gene's symbol, name, other symbols and location.
- The Human Phenotype Ontology, release 2026-09-01: the traits linked to the gene. Find out more at hpo.jax.org.
Cite this page
Dante Labs. (n.d.). MT-TN gene: mitochondrially encoded tRNA-Asn (AAU/C). Retrieved 16 October 2026, from https://dantelabs.com/genes/mt-tn
Dante Labs. MT-TN gene: mitochondrially encoded tRNA-Asn (AAU/C) [Internet]. [cited 16 October 2026]. Available from: https://dantelabs.com/genes/mt-tn
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