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page$trait$nameRead the genes linked to Breathing dysregulation, and the rest of your genome, with one test.
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Get my Genome Test24 condition reports read genes linked to this trait
Dante Labs condition reports look at the genes behind groups of inherited conditions, read from one whole-genome test. Each page says which conditions and genes a report covers, how it is read and what it cannot tell you.
- Inherited Congenital Heart DefectsReads 7 of these genesACTC1GATA4GATA6MYH6NKX2-5TBX20About this report →
- Hirschsprung Disease & Related Enteric NeurocristopathiesReads 2 of these genesPHOX2BRETAbout this report →
- Congenital Central Hypoventilation SyndromeReads 1 of these genesPHOX2BAbout this report →
- KYNU-Related Congenital NAD DeficiencyReads 1 of these genesKYNUAbout this report →
Show 20 more reports
- Neuroblastoma Predisposition (ALK and PHOX2B)Reads 1 of these genesPHOX2BAbout this report →
- Tetralogy of FallotReads 1 of these genesNKX2-5About this report →
- Neonatal Diabetes MellitusReads 2 of these genesGATA4GATA6About this report →
- Syndromic and Metabolic CardiomyopathiesReads 1 of these genesNKX2-5About this report →
- Left Ventricular NoncompactionReads 1 of these genesACTC1About this report →
- Diabetes MellitusReads 2 of these genesGATA4GATA6About this report →
- Thyroid CancerReads 2 of these genesRETNKX2-5About this report →
- Malignant Endocrine NeoplasmReads 1 of these genesRETAbout this report →
- Hereditary Pheochromocytoma and ParagangliomaReads 1 of these genesRETAbout this report →
- Meckel SyndromeReads 1 of these genesTMEM67About this report →
- Urinary and Renal System TumourReads 1 of these genesRETAbout this report →
- Dilated CardiomyopathyReads 2 of these genesACTC1TBX20About this report →
- Hypertrophic CardiomyopathyReads 2 of these genesACTC1MYH6About this report →
- 46,XY Differences of Sex Development and Gonadal DysgenesisReads 1 of these genesGATA4About this report →
- Congenital HypothyroidismReads 1 of these genesNKX2-5About this report →
- Nephronophthisis and Senior-Løken SyndromeReads 1 of these genesTMEM67About this report →
- Joubert Syndrome And Related DisordersReads 1 of these genesTMEM67About this report →
- Autosomal Recessive Cerebellar Ataxias (incl. CANVAS and AVED)Reads 1 of these genesTMEM67About this report →
- Primary Mitochondrial DiseaseReads 1 of these genesNDUFS6About this report →
- Inherited Neurodegenerative DisordersReads 1 of these genesTMEM67About this report →
Read the genes linked to Breathing dysregulation, and the rest of your genome, with one test.
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Get my Genome Test14 genes linked to Breathing dysregulation
Changes in these genes cause rare conditions in which Breathing dysregulation is seen. Most people with this trait have none of those conditions, and a gene on this list says nothing about anyone's own genome.
| Gene | How often it is seen | Conditions |
|---|---|---|
| ASCL1achaete-scute family bHLH transcription factor 1 | Very often (80–99%) | In 1 condition |
| PHOX2Bpaired like homeobox 2B | Very often (80–99%) | In 1 condition |
| RETret proto-oncogene | Very often (80–99%) | In 1 condition |
| KYNUkynureninase | Often (30–79%) | In 1 condition |
| ACTC1actin alpha cardiac muscle 1 | Sometimes (5–29%) | In 1 condition |
| CITED2Cbp/p300 interacting transactivator with ED-rich tail 2 | Sometimes (5–29%) | In 1 condition |
| GATA4GATA binding protein 4 | Sometimes (5–29%) | In 1 condition |
| GATA6GATA binding protein 6 | Sometimes (5–29%) | In 1 condition |
| MYH6myosin heavy chain 6 | Sometimes (5–29%) | In 1 condition |
| NKX2-5NK2 homeobox 5 | Sometimes (5–29%) | In 1 condition |
| TBX20T-box transcription factor 20 | Sometimes (5–29%) | In 1 condition |
| TLL1tolloid like 1 | Sometimes (5–29%) | In 1 condition |
| NDUFS6NADH:ubiquinone oxidoreductase subunit S6 | Not recorded | In 1 condition |
| TMEM67transmembrane protein 67 | Not recorded | In 1 condition |
How often is among people with one of the gene's conditions, the most often across them, as the Human Phenotype Ontology records it. These pages describe traits and the research behind them; they are not a diagnosis, and a doctor or genetic counsellor is the person to ask about symptoms.
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Where this comes from
- The Human Phenotype Ontology, release 2026-09-01: the trait, its names, its definition and the genes linked to it. Find out more at hpo.jax.org.
- Data release 2026.10.19-9814e911.
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