Gene
DUSP6
dual specificity phosphatase 6
- HGNC 3072↗(opens in a new tab)
- Ensembl gene ENSG00000139318↗(opens in a new tab)
- NCBI Gene 1848↗(opens in a new tab)
Summary
- Cytogenetic location
- 12q21.33
- Coordinates
- Chromosome 12: 89,347,235–89,352,501 (GRCh38)
- Exons
- 3 exons across 5.3 kb
- Protein
- 381 amino acids
- Also known as
- MKP-3, PYST1
- MANE Select transcript
- ENST00000279488.8NM_001946.4
- 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 DUSP6 yet. The test sequences your whole genome, so your data includes it all the same.
How DUSP6 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 3.6 kb of the gene's 5.3 kb; 1,146 of those bases code for the protein.
How a genome test reads DUSP6
1
position in DUSP6 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 5.3 kb of DUSP6, introns included, not only the 3.6 kb of exons.
Traits linked to DUSP6
The Human Phenotype Ontology lists these as features of the rare conditions DUSP6 can cause. Each trait's page lists the other genes linked to it.
Abnormality of the musculoskeletal system
- Delayed bone maturation
- Low solidness and mass of the bones
- Osteopenia
- Osteoporosis
- Abnormal skeletal development
- Hypermobility of all joints
- Low muscle tone
- Muscle weakness
Show 2 more traits
Abnormality of the endocrine system
- Hypogonadotropic hypogonadism
- Absence of pubertal development
- Absence of secondary sex characteristics
- Anterior hypopituitarism
- Decreased function of male gonad
- Decreased serum testosterone level
- Delayed puberty
- Female hypogonadism
Show 1 more trait
Abnormality of the nervous system
- Anxiety
- Depression
- Abnormal gait
- Ataxia
- Difficulty articulating speech
- Epilepsy
- Hand mirror movements
- Leg paralysis
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.). DUSP6 gene: dual specificity phosphatase 6. Retrieved 17 October 2026, from https://dantelabs.com/genes/dusp6
Dante Labs. DUSP6 gene: dual specificity phosphatase 6 [Internet]. [cited 17 October 2026]. Available from: https://dantelabs.com/genes/dusp6
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