Gene
NKX2-6
NK2 homeobox 6
- HGNC 32940↗(opens in a new tab)
- Ensembl gene ENSG00000180053↗(opens in a new tab)
- NCBI Gene 137814↗(opens in a new tab)
Summary
- Cytogenetic location
- 8p21.2
- Coordinates
- Chromosome 8: 23,701,740–23,706,756 (GRCh38)
- Exons
- 2 exons across 5 kb
- Protein
- 301 amino acids
- Also known as
- CSX2, NKX4-2
- MANE Select transcript
- ENST00000325017.4NM_001136271.3
- 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 NKX2-6 yet. The test sequences your whole genome, so your data includes it all the same.
How NKX2-6 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 1.8 kb of the gene's 5 kb; 906 of those bases code for the protein.
How a genome test reads NKX2-6
4
positions in NKX2-6 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 5 kb of NKX2-6, introns included, not only the 1.8 kb of exons.
Traits linked to NKX2-6
The Human Phenotype Ontology lists these as features of the rare conditions NKX2-6 can cause. Each trait's page lists the other genes linked to it.
Abnormality of the cardiovascular system
- Fainting spell
- Palpitations
- Quivering upper heart chambers resulting in irregular heartbeat
- Tetralogy of Fallot
- Heart attack
- Complete atrioventricular canal defect
- Double outlet right ventricle
- Narrowing of aorta
Show 2 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.). NKX2-6 gene: NK2 homeobox 6. Retrieved 16 October 2026, from https://dantelabs.com/genes/nkx2-6
Dante Labs. NKX2-6 gene: NK2 homeobox 6 [Internet]. [cited 16 October 2026]. Available from: https://dantelabs.com/genes/nkx2-6
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