Gene
ATP6V0C
ATPase H+ transporting V0 subunit c
- HGNC 855↗(opens in a new tab)
- Ensembl gene ENSG00000185883↗(opens in a new tab)
- NCBI Gene 527↗(opens in a new tab)
Summary
- Cytogenetic location
- 16p13.3
- Coordinates
- Chromosome 16: 2,513,952–2,520,218 (GRCh38)
- Exons
- 3 exons across 6.3 kb
- Protein
- 155 amino acids
- Also known as
- VATL, Vma3
- Previous symbols
- ATPL, ATP6C, ATP6L
- MANE Select transcript
- ENST00000330398.9NM_001694.4
- Locus type
- Protein-coding
- Very high
- Confident
- Low
- Very low
This page as data
Add .json to the page's address, or ask for application/json, to read it as JSON.
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No Genome Test report reads ATP6V0C yet. The test sequences your whole genome, so your data includes it all the same.
How ATP6V0C 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 1.1 kb of the gene's 6.3 kb; 468 of those bases code for the protein.
Sequencing ATP6V0C
4
positions in ATP6V0C 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 6.3 kb of ATP6V0C, introns included, not only the 1.1 kb of exons.
Traits linked to ATP6V0C
The Human Phenotype Ontology lists these as features of the rare conditions ATP6V0C can cause. Each trait's page lists the other genes linked to it.
Abnormality of the nervous system
- Absent speech development
- Bilateral tonic-clonic seizure with focal onset
- Brief seizures with staring spells
- Delayed speech and language development
- Febrile seizure (within the age range of 3 months to 6 years)
- Focal impaired awareness seizure
- Grand mal seizures
- Infantile spasms
Show 12 more traits
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.). ATP6V0C gene: ATPase H+ transporting V0 subunit c. Retrieved 17 October 2026, from https://dantelabs.com/genes/atp6v0c
Dante Labs. ATP6V0C gene: ATPase H+ transporting V0 subunit c [Internet]. [cited 17 October 2026]. Available from: https://dantelabs.com/genes/atp6v0c
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