MT-TP
geneOn this page
Also known as trnP
Summary
MT-TP (mitochondrially encoded tRNA-Pro (CCN), HGNC:7494) 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:7494 |
| Approved symbol | MT-TP |
| Name | mitochondrially encoded tRNA-Pro (CCN) |
| Location | mitochondria |
| Locus type | RNA, transfer |
| Status | Approved |
| Aliases | trnP |
| Ensembl gene | ENSG00000210196 |
| Ensembl biotype | Mt_tRNA |
| OMIM | 590075 |
| Entrez | 4571 |
| RNAcentral | URS000002176F — tRNA, 68 nt, 5 organism(s) |
Gene structure
Transcript identifiers
Ensembl transcripts: 1 — 1 Mt_tRNA
ENST00000387461
RefSeq mRNA: 0 — MANE Select: None
Canonical transcript exons
ENST00000387461 — 1 exons
| Exon | Start | End |
|---|---|---|
| ENSE00001544473 | 15956 | 16023 |
Expression profiles
Bgee: expression breadth ubiquitous, 118 present calls, max score 99.98.
FANTOM5 (CAGE): breadth broad, TPM avg 3.0843 / max 1031.2089, expressed in 645 samples.
FANTOM5 promoters (2 alternative TSS)
| Promoter ID | TPM avg | Samples expressed |
|---|---|---|
| 195302 | 1.8048 | 260 |
| 195303 | 1.2795 | 441 |
Top tissues by expression
118 total, by Bgee expression score (0-100, higher = more expressed):
| Tissue | Anatomy ID | Expression score | Quality |
|---|---|---|---|
| rectum | UBERON:0001052 | 99.98 | gold quality |
| smooth muscle tissue | UBERON:0001135 | 99.97 | gold quality |
| mucosa of stomach | UBERON:0001199 | 99.97 | gold quality |
| right uterine tube | UBERON:0001302 | 99.96 | gold quality |
| caudate nucleus | UBERON:0001873 | 99.96 | gold quality |
| putamen | UBERON:0001874 | 99.96 | gold quality |
| amygdala | UBERON:0001876 | 99.96 | gold quality |
| nucleus accumbens | UBERON:0001882 | 99.96 | gold quality |
| hypothalamus | UBERON:0001898 | 99.96 | gold quality |
| right hemisphere of cerebellum | UBERON:0014890 | 99.96 | gold quality |
| skeletal muscle tissue | UBERON:0001134 | 99.95 | gold quality |
| fundus of stomach | UBERON:0001160 | 99.95 | gold quality |
| frontal cortex | UBERON:0001870 | 99.95 | gold quality |
| Ammon’s horn | UBERON:0001954 | 99.95 | gold quality |
| substantia nigra | UBERON:0002038 | 99.95 | gold quality |
| apex of heart | UBERON:0002098 | 99.95 | gold quality |
| cerebellar hemisphere | UBERON:0002245 | 99.95 | gold quality |
| right frontal lobe | UBERON:0002810 | 99.95 | gold quality |
| olfactory segment of nasal mucosa | UBERON:0005386 | 99.95 | gold quality |
| dorsolateral prefrontal cortex | UBERON:0009834 | 99.95 | gold quality |
| granulocyte | CL:0000094 | 99.94 | gold quality |
| cerebral cortex | UBERON:0000956 | 99.94 | gold quality |
| endometrium | UBERON:0001295 | 99.94 | gold quality |
| heart left ventricle | UBERON:0002084 | 99.94 | gold quality |
| right testis | UBERON:0004534 | 99.94 | gold quality |
| right atrium auricular region | UBERON:0006631 | 99.94 | gold quality |
| Brodmann (1909) area 9 | UBERON:0013540 | 99.94 | gold quality |
| adrenal tissue | UBERON:0018303 | 99.94 | gold quality |
| adult mammalian kidney | UBERON:0000082 | 99.93 | gold quality |
| heart | UBERON:0000948 | 99.93 | gold quality |
Single-cell (SCXA)
Detected in 2 experiment(s), a significant marker in 2.
| Experiment | Marker? | Max mean expression |
|---|---|---|
| E-HCAD-30 | yes | 489.37 |
| E-ANND-3 | no | 0.00 |
Regulation
Is transcription factor: no
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, myopathy, Parkinson disease, mitochondrial