Gene
MT-TI
mitochondrially encoded tRNA-Ile (AUU/C)
- HGNC 7488↗(opens in a new tab)
- Ensembl gene ENSG00000210100↗(opens in a new tab)
- NCBI Gene 4565↗(opens in a new tab)
Summary
- Cytogenetic location
- mitochondria
- Inheritance
- Autosomal dominant
- Also known as
- trnI
- Previous symbols
- MTTI
- Locus type
- RNA, transfer
Reference genomeGRCh38hg38
Positions on gene and variant pages follow this choice, in this browser.
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Hypertrophic Cardiomyopathy
- Autosomal dominant
One of 62 genes linked to it
A condition in which the myocardium is hypertrophied without an obvious cause. The hypertrophy is generally asymmetric and may be associated with obstruction of the ventricular outflow tract.
- ClinGen rates the link moderate
What knowing changes
Beta-blockers, non-dihydropyridine calcium channel blockers, activity restriction, genetic counseling
Inheritance
- Autosomal dominant
- One changed copy, from either parent, is enough. A parent who has one passes it on to each child with a one-in-two chance.
How a genome test reads MT-TI
1
position in MT-TI where ClinVar classes a change as pathogenic or likely pathogenic
None of them falls in a region short reads find hard.
Genes linked to the same conditions
- ACADVLacyl-CoA dehydrogenase very long chainShares 1 condition
- ACTC1actin alpha cardiac muscle 1Shares 1 condition
- ALPK3alpha kinase 3Shares 1 condition
- BRAFB-Raf proto-oncogene, serine/threonine kinaseShares 1 condition
- CDKN1Ccyclin dependent kinase inhibitor 1CShares 1 condition
- CSRP3cysteine and glycine rich protein 3Shares 1 condition
- DHHdesert hedgehog signaling moleculeShares 1 condition
- DHX37DEAH-box helicase 37Shares 1 condition
- DMPKDM1 protein kinaseShares 1 condition
- ERFETS2 repressor factorShares 1 condition
- ETFAelectron transfer flavoprotein subunit alphaShares 1 condition
- ETFBelectron transfer flavoprotein subunit betaShares 1 condition
Traits linked to MT-TI
The Human Phenotype Ontology lists these as features of the rare conditions MT-TI can cause. Each trait's page lists the other genes linked to it.
External links
Where this comes from
- HGNC: the gene's symbol, name, other symbols and location.
- GenCC and ClinGen, released 2026-10-16: which conditions the gene is linked to, and how strongly.
- The ACMG secondary findings list, SF v3.2.
- ClinVar and the GIAB stratifications: known disease-causing sites, and the regions short reads find hard.
- The Human Phenotype Ontology, release 2026-09-01: the traits linked to the gene. Find out more at hpo.jax.org.
- Data release 2026.10.16-c6eea6bf.
Cite this page
Dante Labs. (n.d.). MT-TI gene: mitochondrially encoded tRNA-Ile (AUU/C). Retrieved 17 October 2026, from https://dantelabs.com/genes/mt-ti
Dante Labs. MT-TI gene: mitochondrially encoded tRNA-Ile (AUU/C) [Internet]. [cited 17 October 2026]. Available from: https://dantelabs.com/genes/mt-ti
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