Trait
Episodic tachypnea
Episodes of very rapid breathing.
Summary
- Also called
- Hyperpnea, episodic
- Body system
- Abnormality of the respiratory system
Reference genomeGRCh38hg38
Positions on gene and variant pages follow this choice, in this browser.
Read the genes linked to Episodic tachypnea, and the rest of your genome, with one test.
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Get my Genome Test46 genes linked to Episodic tachypnea
Changes in these genes cause rare conditions in which Episodic tachypnea 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 |
|---|---|---|
| AHI1Abelson helper integration site 1 | Very often (80–99%) | In 2 conditions |
| ARL13BARF like GTPase 13B | Very often (80–99%) | In 1 condition |
| ARL3ARF like GTPase 3 | Very often (80–99%) | In 1 condition |
| ARMC9armadillo repeat containing 9 | Very often (80–99%) | In 1 condition |
| B9D1B9 domain containing 1 | Very often (80–99%) | In 1 condition |
| B9D2B9 domain containing 2 | Very often (80–99%) | In 1 condition |
| CBY1chibby 1, beta catenin antagonist | Very often (80–99%) | In 1 condition |
| CEP104centrosomal protein 104 | Very often (80–99%) | In 1 condition |
| CEP120centrosomal protein 120 | Very often (80–99%) | In 1 condition |
| CEP41centrosomal protein 41 | Very often (80–99%) | In 1 condition |
| CPLANE1ciliogenesis and planar polarity effector complex subunit 1 | Very often (80–99%) | In 2 conditions |
| CSPP1centrosome and spindle pole associated protein 1 | Very often (80–99%) | In 1 condition |
| HYLS1HYLS1 centriolar and ciliogenesis associated | Very often (80–99%) | In 1 condition |
| IFT74intraflagellar transport 74 | Very often (80–99%) | In 1 condition |
| INPP5Einositol polyphosphate-5-phosphatase E | Very often (80–99%) | In 2 conditions |
| KATNIPkatanin interacting protein | Very often (80–99%) | In 1 condition |
| KIAA0586KIAA0586 | Very often (80–99%) | In 1 condition |
| KIAA0753KIAA0753 | Very often (80–99%) | In 2 conditions |
| MKS1MKS transition zone complex subunit 1 | Very often (80–99%) | In 1 condition |
| OFD1OFD1 centriole and centriolar satellite protein | Very often (80–99%) | In 2 conditions |
| PDE6Dphosphodiesterase 6D | Very often (80–99%) | In 2 conditions |
| PIBF1progesterone immunomodulatory binding factor 1 | Very often (80–99%) | In 1 condition |
| SUFUSUFU negative regulator of hedgehog signaling | Very often (80–99%) | In 1 condition |
| TCTN1tectonic family member 1 | Very often (80–99%) | In 1 condition |
| TCTN2tectonic family member 2 | Very often (80–99%) | In 1 condition |
| TCTN3tectonic family member 3 | Very often (80–99%) | In 2 conditions |
| TMEM218transmembrane protein 218 | Very often (80–99%) | In 1 condition |
| TMEM237transmembrane protein 237 | Very often (80–99%) | In 1 condition |
| TMEM67transmembrane protein 67 | Very often (80–99%) | In 1 condition |
| TOGARAM1TOG array regulator of axonemal microtubules 1 | Very often (80–99%) | In 1 condition |
| CC2D2Acoiled-coil and C2 domain containing 2A | Often (30–79%) | In 1 condition |
| CDKL5cyclin dependent kinase like 5 | Often (30–79%) | In 1 condition |
| GABBR2gamma-aminobutyric acid type B receptor subunit 2 | Often (30–79%) | In 1 condition |
| MECP2methyl-CpG binding protein 2 | Often (30–79%) | In 1 condition |
| NTNG1netrin G1 | Often (30–79%) | In 1 condition |
| SMC1Astructural maintenance of chromosomes 1A | Often (30–79%) | In 1 condition |
| UQCRC2ubiquinol-cytochrome c reductase core protein 2 | Often (30–79%) | In 1 condition |
| ACADVLacyl-CoA dehydrogenase very long chain | Sometimes (5–29%) | In 1 condition |
| FAM149B1family with sequence similarity 149 member B1 | Sometimes (5–29%) | In 1 condition |
| FBP1fructose-bisphosphatase 1 | Sometimes (5–29%) | In 1 condition |
Show 6 more genes
| Gene | How often it is seen | Conditions |
|---|---|---|
| KIF7kinesin family member 7 | Sometimes (5–29%) | In 1 condition |
| TMEM216transmembrane protein 216 | Sometimes (5–29%) | In 2 conditions |
| TMEM231transmembrane protein 231 | Sometimes (5–29%) | In 1 condition |
| TOPORSTOP1 binding arginine/serine rich protein, E3 ubiquitin ligase | Sometimes (5–29%) | In 1 condition |
| CEP290centrosomal protein 290 | Not recorded | In 1 condition |
| RPGRIP1LRPGRIP1 like | 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.
Broader traits
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 2026.10.16-c6eea6bf.
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