MT-TR
geneOn this page
Also known as trnR
Summary
MT-TR (mitochondrially encoded tRNA-Arg (CGN), HGNC:7496) is a mitochondrial tRNA gene on chromosome mitochondria.
At a glance
- Gene type: non-coding (Mt_tRNA) — no protein product; not a drug target. Variant/disease associations are omitted (they would be positional, from an overlapping protein-coding gene).
Identifiers
Gene identifiers
| Field | Value |
|---|---|
| HGNC ID | HGNC:7496 |
| Approved symbol | MT-TR |
| Name | mitochondrially encoded tRNA-Arg (CGN) |
| Location | mitochondria |
| Locus type | RNA, transfer |
| Status | Approved |
| Aliases | trnR |
| Ensembl gene | ENSG00000210174 |
| Ensembl biotype | Mt_tRNA |
| OMIM | 590005 |
| Entrez | 4573 |
| RNAcentral | URS00005983A6 — tRNA, 65 nt, 6 organism(s) |
Gene structure
Transcript identifiers
Ensembl transcripts: 1 — 1 Mt_tRNA
ENST00000387439
RefSeq mRNA: 0 — MANE Select: None
Canonical transcript exons
ENST00000387439 — 1 exons
| Exon | Start | End |
|---|---|---|
| ENSE00001544482 | 10405 | 10469 |
Expression profiles
Bgee: expression breadth ubiquitous, 116 present calls, max score 99.49.
FANTOM5 (CAGE): breadth tissue_specific, TPM avg 0.3811 / max 55.5352, expressed in 117 samples.
FANTOM5 promoters (1 alternative TSS)
| Promoter ID | TPM avg | Samples expressed |
|---|---|---|
| 194923 | 0.3811 | 117 |
Top tissues by expression
116 total, by Bgee expression score (0-100, higher = more expressed):
| Tissue | Anatomy ID | Expression score | Quality |
|---|---|---|---|
| sural nerve | UBERON:0015488 | 99.49 | gold quality |
| skeletal muscle tissue | UBERON:0001134 | 99.20 | gold quality |
| apex of heart | UBERON:0002098 | 99.01 | gold quality |
| caudate nucleus | UBERON:0001873 | 97.68 | gold quality |
| putamen | UBERON:0001874 | 97.62 | gold quality |
| amygdala | UBERON:0001876 | 97.60 | gold quality |
| substantia nigra | UBERON:0002038 | 97.27 | gold quality |
| Ammon’s horn | UBERON:0001954 | 97.22 | gold quality |
| nucleus accumbens | UBERON:0001882 | 96.95 | gold quality |
| hypothalamus | UBERON:0001898 | 96.79 | gold quality |
| right frontal lobe | UBERON:0002810 | 96.13 | gold quality |
| heart left ventricle | UBERON:0002084 | 96.06 | gold quality |
| frontal cortex | UBERON:0001870 | 95.98 | gold quality |
| anterior cingulate cortex | UBERON:0009835 | 95.87 | gold quality |
| prefrontal cortex | UBERON:0000451 | 95.13 | gold quality |
| adult mammalian kidney | UBERON:0000082 | 94.69 | gold quality |
| C1 segment of cervical spinal cord | UBERON:0006469 | 94.29 | gold quality |
| cerebral cortex | UBERON:0000956 | 94.12 | gold quality |
| right adrenal gland cortex | UBERON:0035827 | 93.42 | gold quality |
| brain | UBERON:0000955 | 92.86 | gold quality |
| heart | UBERON:0000948 | 91.63 | gold quality |
| right adrenal gland | UBERON:0001233 | 91.34 | gold quality |
| adrenal gland | UBERON:0002369 | 90.66 | gold quality |
| kidney | UBERON:0002113 | 90.52 | gold quality |
| left adrenal gland | UBERON:0001234 | 90.45 | gold quality |
| bone marrow | UBERON:0002371 | 90.41 | gold quality |
| dorsolateral prefrontal cortex | UBERON:0009834 | 90.29 | gold quality |
| left adrenal gland cortex | UBERON:0035825 | 90.03 | gold quality |
| placenta | UBERON:0001987 | 89.99 | gold quality |
| right hemisphere of cerebellum | UBERON:0014890 | 89.96 | gold quality |
Single-cell (SCXA)
Detected in 1 experiment(s), a significant marker in 0.
| Experiment | Marker? | Max mean expression |
|---|---|---|
| E-ANND-3 | no | 0.00 |
Regulation
Is transcription factor: no
Literature-anchored findings (GeneRIF, showing 1)
- A novel mitochondrial tRNA Arg mutation resulting in an anticodon swap in a patient with mitochondrial encephalomyopathy. (PMID:22781096)
Cross-species orthologs
0 orthologs
Protein
Non-coding RNA — no protein product; not a drug target.
Function
No curated pathway, Gene-Ontology, or interaction data.
Disease & clinical
No curated disease, variant, or cancer-driver associations.
Drugs & pharmacology
No drug or pharmacology data — not an established drug target.
Related Atlas pages
- Disease cohort memberships (association, not causation — diseases whose associated-gene cohort lists this gene; a subset are also under Associated diseases): MELAS syndrome, MERRF syndrome, mitochondrial encephalomyopathy