Gene
TRMT10A
tRNA methyltransferase 10A
- HGNC 28403↗(opens in a new tab)
- Ensembl gene ENSG00000145331↗(opens in a new tab)
- NCBI Gene 93587↗(opens in a new tab)
Summary
- Cytogenetic location
- 4q23
- Coordinates
- Chromosome 4: 99,546,711–99,564,039 (GRCh38)
- Exons
- 8 exons across 17.3 kb
- Protein
- 339 amino acids
- Also known as
- MGC27034, TRM10
- Previous symbols
- RG9MTD2
- MANE Select transcript
- ENST00000394876.7NM_001134665.3
- Locus type
- gene with protein product
- Very high
- Confident
- Low
- Very low
Reference genomeGRCh38hg38
Positions on gene and variant pages follow this choice, in this browser.
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No Genome Test report reads TRMT10A yet. The test sequences your whole genome, so your data includes it all the same.
How TRMT10A is laid out
- Coding sequence
- Untranslated region
- Intron
- Direction of transcription
- Known disease-causing sites
- Stretches short reads find hard
Exons of the gene's MANE Select transcript (release v1.5), from NCBI and EMBL-EBI, on the GRCh38 reference genome.
Chromosome bands from UCSC's GRCh38 ideogram (2022-10-29).
Nearby genes from Ensembl release 116, on GRCh38.
Exons make up 3.5 kb of the gene's 17.3 kb; 1,020 of those bases code for the protein.
How a genome test reads TRMT10A
14
positions in TRMT10A where ClinVar classes a change as pathogenic or likely pathogenic
2 of them (14%) fall in regions short reads find hard.
- Low mappability (2 sites)Regions where 100 bp or 250 bp reads cannot be placed uniquely.
A whole genome covers all 17.3 kb of TRMT10A, introns included, not only the 3.5 kb of exons.
Traits linked to TRMT10A
The Human Phenotype Ontology lists these as features of the rare conditions TRMT10A can cause. Each trait's page lists the other genes linked to it.
Abnormality of head or neck
- Abnormally small head
- Small head present at birth
- Abnormal facial shape
- Low frontal hairline
- Short neck
- Wide nose
- Decreased size of teeth
- Downturned corners of mouth
Show 16 more traits
Abnormality of the musculoskeletal system
- Double-Jointed
- Osteoporosis
- Scoliosis
- Funnel chest
- Kyphoscoliosis
- Low muscle tone in trunk
- Rounded shoulders
- Spastic paraparesis
Show 1 more trait
External links
Gene records
Transcript
Protein
Where this comes from
- HGNC: the gene's symbol, name, other symbols and location.
- MANE Select v1.5, from NCBI and EMBL-EBI: the transcript, its exons and coding sequence.
- ClinVar and the GIAB stratifications: known disease-causing sites, and the regions short reads find hard.
- The Human Phenotype Ontology, release 2026-09-01: the traits linked to the gene. Find out more at hpo.jax.org.
- Data release 2026.10.16-c6eea6bf.
Cite this page
Dante Labs. (n.d.). TRMT10A gene: tRNA methyltransferase 10A. Retrieved 16 October 2026, from https://dantelabs.com/genes/trmt10a
Dante Labs. TRMT10A gene: tRNA methyltransferase 10A [Internet]. [cited 16 October 2026]. Available from: https://dantelabs.com/genes/trmt10a
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