MT-TH

gene
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Also known as trnH

Summary

MT-TH (mitochondrially encoded tRNA-His (CAU/C), HGNC:7487) 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 4564 — 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:7487
Approved symbolMT-TH
Namemitochondrially encoded tRNA-His (CAU/C)
Locationmitochondria
Locus typeRNA, transfer
StatusApproved
AliasestrnH
Ensembl geneENSG00000210176
Ensembl biotypeMt_tRNA
OMIM590040
Entrez4564
RNAcentralURS00001FBD75 — tRNA, 69 nt, 3 organism(s)

Gene structure

Transcript identifiers

Ensembl transcripts: 1 — 1 Mt_tRNA

ENST00000387441

RefSeq mRNA: 0 — MANE Select: None

Canonical transcript exons

ENST00000387441 — 1 exons

ExonStartEnd
ENSE000015444801213812206

Expression profiles

Bgee: expression breadth ubiquitous, 118 present calls, max score 99.83.

FANTOM5 (CAGE): breadth broad, TPM avg 4.2637 / max 597.0157, expressed in 733 samples.

FANTOM5 promoters (1 alternative TSS)

Promoter IDTPM avgSamples expressed
1949724.2637733

Top tissues by expression

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

TissueAnatomy IDExpression scoreQuality
sural nerveUBERON:001548899.83gold quality
apex of heartUBERON:000209899.49gold quality
putamenUBERON:000187498.76gold quality
caudate nucleusUBERON:000187398.55gold quality
nucleus accumbensUBERON:000188298.28gold quality
amygdalaUBERON:000187698.05gold quality
substantia nigraUBERON:000203897.88gold quality
skeletal muscle tissueUBERON:000113497.66gold quality
Ammon’s hornUBERON:000195497.64gold quality
hypothalamusUBERON:000189897.61gold quality
heart left ventricleUBERON:000208497.57gold quality
right adrenal gland cortexUBERON:003582797.37gold quality
vermiform appendixUBERON:000115497.33gold quality
anterior cingulate cortexUBERON:000983597.04gold quality
prefrontal cortexUBERON:000045196.93gold quality
mucosa of stomachUBERON:000119996.74gold quality
adult mammalian kidneyUBERON:000008296.55gold quality
left adrenal gland cortexUBERON:003582596.23gold quality
right adrenal glandUBERON:000123396.18gold quality
endometriumUBERON:000129595.95gold quality
duodenumUBERON:000211495.81gold quality
adrenal glandUBERON:000236995.50gold quality
cerebral cortexUBERON:000095695.49gold quality
left adrenal glandUBERON:000123495.37gold quality
frontal cortexUBERON:000187095.31gold quality
right frontal lobeUBERON:000281095.17gold quality
adrenal tissueUBERON:001830394.67gold quality
C1 segment of cervical spinal cordUBERON:000646994.59gold quality
brainUBERON:000095594.07gold quality
kidneyUBERON:000211394.01gold quality

Single-cell (SCXA)

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

ExperimentMarker?Max mean expression
E-ANND-3no0.91

Regulation

Is transcription factor: no

Literature-anchored findings (GeneRIF, showing 3)

  • The findings demonstrate the pathogenic mechanism leading to an impaired oxidative phosphorylation in cybrid cell lines carrying the deafness-associated tRNAHis 12201T>C mutation. (PMID:24920829)
  • We also detected in 4 asthenospermic patients a double novels mutations, the first was found in COXII gene (m.8021 G/A) that was absent in normospermic infertile men. (PMID:24931671)
  • Whole mitochondrial genome analysis in Chinese patients with keratoconus. (PMID:34012229)

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.