MT-TG
geneOn this page
Also known as trnG
Summary
MT-TG (mitochondrially encoded tRNA-Gly (GGN), HGNC:7486) 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:7486 |
| Approved symbol | MT-TG |
| Name | mitochondrially encoded tRNA-Gly (GGN) |
| Location | mitochondria |
| Locus type | RNA, transfer |
| Status | Approved |
| Aliases | trnG |
| Ensembl gene | ENSG00000210164 |
| Ensembl biotype | Mt_tRNA |
| OMIM | 590035 |
| Entrez | 4563 |
| RNAcentral | URS00000C6674 — tRNA, 68 nt, 8 organism(s) |
Gene structure
Transcript identifiers
Ensembl transcripts: 1 — 1 Mt_tRNA
ENST00000387429
RefSeq mRNA: 0 — MANE Select: None
Canonical transcript exons
ENST00000387429 — 1 exons
| Exon | Start | End |
|---|---|---|
| ENSE00001544483 | 9991 | 10058 |
Expression profiles
Bgee: expression breadth ubiquitous, 117 present calls, max score 99.57.
FANTOM5 (CAGE): breadth tissue_specific, TPM avg 0.7567 / max 325.6449, expressed in 180 samples.
FANTOM5 promoters (2 alternative TSS)
| Promoter ID | TPM avg | Samples expressed |
|---|---|---|
| 194913 | 0.5805 | 149 |
| 194914 | 0.1763 | 56 |
Top tissues by expression
117 total, by Bgee expression score (0-100, higher = more expressed):
| Tissue | Anatomy ID | Expression score | Quality |
|---|---|---|---|
| apex of heart | UBERON:0002098 | 99.57 | gold quality |
| sural nerve | UBERON:0015488 | 99.49 | gold quality |
| skeletal muscle tissue | UBERON:0001134 | 99.32 | gold quality |
| putamen | UBERON:0001874 | 99.19 | gold quality |
| caudate nucleus | UBERON:0001873 | 99.17 | gold quality |
| amygdala | UBERON:0001876 | 99.08 | gold quality |
| substantia nigra | UBERON:0002038 | 98.96 | gold quality |
| Ammon’s horn | UBERON:0001954 | 98.95 | gold quality |
| nucleus accumbens | UBERON:0001882 | 98.94 | gold quality |
| hypothalamus | UBERON:0001898 | 98.85 | gold quality |
| anterior cingulate cortex | UBERON:0009835 | 98.38 | gold quality |
| right frontal lobe | UBERON:0002810 | 98.19 | gold quality |
| heart left ventricle | UBERON:0002084 | 98.13 | gold quality |
| frontal cortex | UBERON:0001870 | 97.86 | gold quality |
| right adrenal gland cortex | UBERON:0035827 | 97.73 | gold quality |
| cerebral cortex | UBERON:0000956 | 97.46 | gold quality |
| C1 segment of cervical spinal cord | UBERON:0006469 | 97.45 | gold quality |
| prefrontal cortex | UBERON:0000451 | 97.23 | gold quality |
| endometrium | UBERON:0001295 | 96.97 | gold quality |
| right adrenal gland | UBERON:0001233 | 96.85 | gold quality |
| vermiform appendix | UBERON:0001154 | 96.61 | gold quality |
| left adrenal gland cortex | UBERON:0035825 | 96.39 | gold quality |
| granulocyte | CL:0000094 | 96.37 | gold quality |
| monocyte | CL:0000576 | 96.26 | gold quality |
| leukocyte | CL:0000738 | 96.26 | gold quality |
| lymph node | UBERON:0000029 | 96.22 | gold quality |
| adult mammalian kidney | UBERON:0000082 | 96.21 | gold quality |
| left adrenal gland | UBERON:0001234 | 96.12 | gold quality |
| adrenal gland | UBERON:0002369 | 95.96 | gold quality |
| dorsolateral prefrontal cortex | UBERON:0009834 | 95.90 | gold quality |
Single-cell (SCXA)
Detected in 1 experiment(s), a significant marker in 0.
| Experiment | Marker? | Max mean expression |
|---|---|---|
| E-ANND-3 | no | 0.12 |
Regulation
Is transcription factor: no
Literature-anchored findings (GeneRIF, showing 2)
- Mitochondrial tRNA(Glu) variant modulate the phenotype of deafness-associated 12S rRNA A1555G mutation in Chinese family. (PMID:19376484)
- Molecular characterization of a Chinese pedigree carrying the hypertension-associated mitochondrial tRNAGln T4363C mutation has been reported. (PMID:28849157)
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): familial hypertrophic cardiomyopathy, MELAS syndrome