Skip to content
Use your HSA or FSA funds

Gene

KCNV2

potassium voltage-gated channel modifier subfamily V member 2

Summary

Cytogenetic location
9p24.2
Coordinates
Chromosome 9: 2,717,510–2,730,037 (GRCh38)
Exons
2 exons across 12.5 kb
Protein
545 amino acids
Also known as
Kv8.2
MANE Select transcript
ENST00000382082.4NM_133497.4
Locus type
gene with protein product
  • Very high
  • Confident
  • Low
  • Very low

Reference genomeGRCh38

Positions on gene and variant pages follow this choice, in this browser.

Curated reports relevant to this gene

No Genome Test report reads KCNV2 yet. The test sequences your whole genome, so your data includes it all the same.

How KCNV2 is laid out

  • Coding sequence
  • Untranslated region
  • Intron
  • Direction of transcription
  • Known disease-causing sites
  • Stretches short reads find hard
Chromosome 9, with a bracket where KCNV2 sits. KCNV2 and 3 genes near it on chromosome 9, from 2,223,774 to 3,223,773.Chromosome 99p24.2p24.3p24.2p24.1p23p22.3p22.2p22.1p21.3p21.2p21.1p13.3p13.2p13.1p12p11.2p11.1q11q12q13q21.11q21.12q21.13q21.2q21.31q21.32q21.33q22.1q22.2q22.31q22.32q22.33q31.1q31.2q31.3q32q33.1q33.2q33.3q34.11q34.12q34.13q34.2q34.32.4 Mb2.6 Mb2.8 Mb3 Mb3.2 MbVLDLR: 2,621,182–2,660,056, forward strandVLDLRPUM3: 2,715,909–2,844,130, reverse strandPUM3KCNV2: 2,717,510–2,730,037, forward strandKCNV2RFX3: 3,218,297–3,526,919, reverse strandRFX3Diagram of KCNV2: 2 exons on the forward strand of chromosome 9Exon 1: 25 known disease-causing sitesExon 2: 4 known disease-causing sitesExon 1: 2,717,510–2,719,095, 1,586 basesExon 2: 2,729,446–2,730,037, 592 bases125′3′

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 12.5 kb; 1,638 of those bases code for the protein.

How a genome test reads KCNV2

29

positions in KCNV2 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 12.5 kb of KCNV2, introns included, not only the 2.2 kb of exons.

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

APA

Dante Labs. (n.d.). KCNV2 gene: potassium voltage-gated channel modifier subfamily V member 2. Retrieved 16 October 2026, from https://dantelabs.com/genes/kcnv2

Vancouver

Dante Labs. KCNV2 gene: potassium voltage-gated channel modifier subfamily V member 2 [Internet]. [cited 16 October 2026]. Available from: https://dantelabs.com/genes/kcnv2

One test. A lifetime of answers.

From $449Free shipping · Results in 6–8 weeks

Get my Genome Test