MT-TS2
geneOn this page
Also known as TRNS2RP8
Summary
MT-TS2 (mitochondrially encoded tRNA-Ser (AGU/C) 2, HGNC:7498) 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:7498 |
| Approved symbol | MT-TS2 |
| Name | mitochondrially encoded tRNA-Ser (AGU/C) 2 |
| Location | mitochondria |
| Locus type | RNA, transfer |
| Status | Approved |
| Aliases | TRNS2, RP8 |
| Ensembl gene | ENSG00000210184 |
| Ensembl biotype | Mt_tRNA |
| OMIM | 590085 |
| Entrez | 4575 |
| RNAcentral | URS00002C130C — tRNA, 59 nt, 5 organism(s) |
Gene structure
Transcript identifiers
Ensembl transcripts: 1 — 1 Mt_tRNA
ENST00000387449
RefSeq mRNA: 0 — MANE Select: None
Canonical transcript exons
ENST00000387449 — 1 exons
| Exon | Start | End |
|---|---|---|
| ENSE00001544479 | 12207 | 12265 |
Expression profiles
Bgee: expression breadth ubiquitous, 116 present calls, max score 99.85.
FANTOM5 (CAGE): breadth ubiquitous, TPM avg 35.4668 / max 10692.0082, expressed in 1648 samples.
FANTOM5 promoters (1 alternative TSS)
| Promoter ID | TPM avg | Samples expressed |
|---|---|---|
| 194974 | 35.4668 | 1648 |
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 | 99.85 | gold quality |
| apex of heart | UBERON:0002098 | 99.78 | gold quality |
| prefrontal cortex | UBERON:0000451 | 99.10 | gold quality |
| right adrenal gland cortex | UBERON:0035827 | 98.85 | gold quality |
| putamen | UBERON:0001874 | 98.82 | gold quality |
| caudate nucleus | UBERON:0001873 | 98.70 | gold quality |
| nucleus accumbens | UBERON:0001882 | 98.33 | gold quality |
| skeletal muscle tissue | UBERON:0001134 | 98.22 | gold quality |
| amygdala | UBERON:0001876 | 98.20 | gold quality |
| substantia nigra | UBERON:0002038 | 98.12 | gold quality |
| heart left ventricle | UBERON:0002084 | 98.02 | gold quality |
| vermiform appendix | UBERON:0001154 | 97.97 | gold quality |
| Ammon’s horn | UBERON:0001954 | 97.83 | gold quality |
| adrenal tissue | UBERON:0018303 | 97.77 | gold quality |
| hypothalamus | UBERON:0001898 | 97.69 | gold quality |
| anterior cingulate cortex | UBERON:0009835 | 97.12 | gold quality |
| duodenum | UBERON:0002114 | 96.86 | gold quality |
| right adrenal gland | UBERON:0001233 | 96.64 | gold quality |
| adrenal gland | UBERON:0002369 | 96.07 | gold quality |
| cerebral cortex | UBERON:0000956 | 95.94 | gold quality |
| mucosa of transverse colon | UBERON:0004991 | 95.89 | gold quality |
| frontal cortex | UBERON:0001870 | 95.88 | gold quality |
| olfactory segment of nasal mucosa | UBERON:0005386 | 95.76 | gold quality |
| endometrium | UBERON:0001295 | 95.75 | gold quality |
| left adrenal gland | UBERON:0001234 | 95.67 | gold quality |
| right frontal lobe | UBERON:0002810 | 95.64 | gold quality |
| granulocyte | CL:0000094 | 95.63 | gold quality |
| left adrenal gland cortex | UBERON:0035825 | 95.39 | gold quality |
| lymph node | UBERON:0000029 | 95.29 | gold quality |
| adult mammalian kidney | UBERON:0000082 | 95.25 | gold quality |
Single-cell (SCXA)
Detected in 3 experiment(s), a significant marker in 1.
| Experiment | Marker? | Max mean expression |
|---|---|---|
| E-MTAB-9543 | yes | 2316.56 |
| E-HCAD-30 | no | 276.06 |
| E-ANND-3 | no | 0.00 |
Regulation
Is transcription factor: no
Literature-anchored findings (GeneRIF, showing 1)
- MTTS2 mutations are an important cause of retinal and syndromic auditory impairment. (PMID:22378285)
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): Kearns-Sayre syndrome, MELAS syndrome, Pearson syndrome, retinitis pigmentosa-deafness syndrome