MT-TQ

gene
On this page

Also known as trnQ

Summary

MT-TQ (mitochondrially encoded tRNA-Gln (CAA/G), HGNC:7495) is a mitochondrial tRNA gene on chromosome mitochondria.

Predicted to enable triplet codon-amino acid adaptor activity. Predicted to be involved in translation.

Source: NCBI Gene 4572 — RefSeq curated summary.

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

FieldValue
HGNC IDHGNC:7495
Approved symbolMT-TQ
Namemitochondrially encoded tRNA-Gln (CAA/G)
Locationmitochondria
Locus typeRNA, transfer
StatusApproved
AliasestrnQ
Ensembl geneENSG00000210107
Ensembl biotypeMt_tRNA
OMIM590030
Entrez4572
RNAcentralURS000019B78E — tRNA, 72 nt, 7 organism(s)

Gene structure

Transcript identifiers

Ensembl transcripts: 1 — 1 Mt_tRNA

ENST00000387372

RefSeq mRNA: 0 — MANE Select: None

Canonical transcript exons

ENST00000387372 — 1 exons

ExonStartEnd
ENSE0000154449443294400

Expression profiles

Bgee: expression breadth ubiquitous, 118 present calls, max score 99.82.

FANTOM5 (CAGE): breadth tissue_specific, TPM avg 0.6600 / max 379.9191, expressed in 148 samples.

FANTOM5 promoters (1 alternative TSS)

Promoter IDTPM avgSamples expressed
1951460.6600148

Top tissues by expression

118 total, by Bgee expression score (0-100, higher = more expressed):

TissueAnatomy IDExpression scoreQuality
skeletal muscle tissueUBERON:000113499.82gold quality
sural nerveUBERON:001548899.66gold quality
apex of heartUBERON:000209899.51gold quality
prefrontal cortexUBERON:000045199.46gold quality
caudate nucleusUBERON:000187399.37gold quality
putamenUBERON:000187499.31gold quality
nucleus accumbensUBERON:000188298.95gold quality
frontal cortexUBERON:000187098.73gold quality
right frontal lobeUBERON:000281098.73gold quality
duodenumUBERON:000211498.72gold quality
heart left ventricleUBERON:000208498.69gold quality
amygdalaUBERON:000187698.61gold quality
substantia nigraUBERON:000203898.59gold quality
Ammon’s hornUBERON:000195498.52gold quality
anterior cingulate cortexUBERON:000983598.08gold quality
rectumUBERON:000105298.00gold quality
vermiform appendixUBERON:000115497.82gold quality
hypothalamusUBERON:000189897.65gold quality
adult mammalian kidneyUBERON:000008297.36gold quality
right adrenal gland cortexUBERON:003582797.16gold quality
cerebral cortexUBERON:000095697.13gold quality
C1 segment of cervical spinal cordUBERON:000646996.90gold quality
adrenal tissueUBERON:001830396.35gold quality
right hemisphere of cerebellumUBERON:001489096.34gold quality
kidneyUBERON:000211396.19gold quality
granulocyteCL:000009495.94gold quality
brainUBERON:000095595.89gold quality
muscle of legUBERON:000138395.76gold quality
right adrenal glandUBERON:000123395.70gold quality
gastrocnemiusUBERON:000138895.68gold quality

Single-cell (SCXA)

Detected in 1 experiment(s), a significant marker in 0.

ExperimentMarker?Max mean expression
E-ANND-3no0.11

Regulation

Is transcription factor: no

Literature-anchored findings (GeneRIF, showing 2)

  • The noncoding mitochondrial sequence alteration (A4401G) at the junction of tRNA(Met) and tRNA(Gln) alters mitochondrial function, implicating this mutation in the pathogenesis of left ventricular hypertrophy in Chinese hypertensives. (PMID:18701880)
  • Data indicate that the 4329C> G point mutation in mitochondrial transfer RNA genes tRNA(Ile) and tRNA(Gln) probably contributed to the pathogenesis of hypertension, possibly in association with other modifying factors. (PMID:25297595)

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.

  • Disease cohort memberships (association, not causation — diseases whose associated-gene cohort lists this gene; a subset are also under Associated diseases): MELAS syndrome, myopathy