Gene
TSEN34
tRNA splicing endonuclease subunit 34
- HGNC 15506↗(opens in a new tab)
- Ensembl gene ENSG00000170892↗(opens in a new tab)
- NCBI Gene 79042↗(opens in a new tab)
Summary
- Cytogenetic location
- 19q13.42
- Coordinates
- Chromosome 19: 54,191,308–54,194,532 (GRCh38)
- Exons
- 4 exons across 3.2 kb
- Protein
- 310 amino acids
- Also known as
- SEN34, SEN34L
- Previous symbols
- LENG5
- MANE Select transcript
- ENST00000396388.3NM_001077446.4
- 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 TSEN34 yet. The test sequences your whole genome, so your data includes it all the same.
How TSEN34 is laid out
- Coding sequence
- Untranslated region
- Intron
- Direction of transcription
- Known disease-causing sites
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 2.2 kb of the gene's 3.2 kb; 933 of those bases code for the protein.
How a genome test reads TSEN34
1
position in TSEN34 where ClinVar classes a change as pathogenic or likely pathogenic
None of them falls in a region short reads find hard.
A whole genome covers all 3.2 kb of TSEN34, introns included, not only the 2.2 kb of exons.
Traits linked to TSEN34
The Human Phenotype Ontology lists these as features of the rare conditions TSEN34 can cause. Each trait's page lists the other genes linked to it.
Abnormality of the nervous system
- Cerebellar vermis hypoplasia
- Choreoathetosis
- Difficulty sleeping
- Epilepsy
- Generalized myoclonic seizure
- Hypoplasia of the ventral pons
- Severe global developmental delay
- Small cerebellum
Show 16 more traits
- Infantile spasms
- Motor delay
- Paroxysmal dystonia
- Small brainstem
- Abnormal cortical gyration
- Babinski sign
- Bilateral tonic-clonic seizure with generalized onset
- Dysplastic corpus callosum
- Simple febrile seizure
- Underdevelopment of part of brain called corpus callosum
- Ventriculomegaly
- Widened cerebellar subarachnoid space
- Cerebellar cyst
- Cerebellar hemisphere hypoplasia
- Chorea
- Dystonia
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.). TSEN34 gene: tRNA splicing endonuclease subunit 34. Retrieved 17 October 2026, from https://dantelabs.com/genes/tsen34
Dante Labs. TSEN34 gene: tRNA splicing endonuclease subunit 34 [Internet]. [cited 17 October 2026]. Available from: https://dantelabs.com/genes/tsen34
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