Trait
Increased respiratory rate or depth of breathing
Clinical name: Tachypnea
Very rapid breathing.
Summary
- Also called
- Polypnea
- Body system
- Abnormality of the respiratory system
Reference genomeGRCh38hg38
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Get my Genome Test58 genes linked to Increased respiratory rate or depth of breathing
Changes in these genes cause rare conditions in which Increased respiratory rate or depth of breathing 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 |
|---|---|---|
| ATP5F1BATP synthase F1 subunit beta | Always | In 1 condition |
| BOLA3bolA family member 3 | Always | In 1 condition |
| COA6cytochrome c oxidase assembly factor 6 | Always | In 1 condition |
| DMRT2doublesex and mab-3 related transcription factor 2 | Always | In 1 condition |
| FARSBphenylalanyl-tRNA synthetase subunit beta | Always | In 1 condition |
| GET3guided entry of tail-anchored proteins factor 3, ATPase | Always | In 1 condition |
| LYRM7LYR motif containing 7 | Always | In 1 condition |
| PTCRApre T cell antigen receptor alpha | Always | In 1 condition |
| SCO2synthesis of cytochrome C oxidase 2 | Always | In 1 condition |
| SFTPCsurfactant protein C | Always | In 2 conditions |
| TM2D3TM2 domain containing 3 | Always | In 1 condition |
| ACAT1acetyl-CoA acetyltransferase 1 | Very often (80–99%) | In 1 condition |
| ACTA2actin alpha 2, smooth muscle | Very often (80–99%) | In 1 condition |
| CC2D2Acoiled-coil and C2 domain containing 2A | Very often (80–99%) | In 1 condition |
| CEP290centrosomal protein 290 | Very often (80–99%) | In 1 condition |
| SFTPBsurfactant protein B | Very often (80–99%) | In 3 conditions |
| TMEM138transmembrane protein 138 | Very often (80–99%) | In 1 condition |
| TMEM216transmembrane protein 216 | Very often (80–99%) | In 1 condition |
| TMEM231transmembrane protein 231 | Very often (80–99%) | In 1 condition |
| TMEM237transmembrane protein 237 | Very often (80–99%) | In 1 condition |
| ZNF423zinc finger protein 423 | Very often (80–99%) | In 1 condition |
| ABCA3ATP binding cassette subfamily A member 3 | Often (30–79%) | In 2 conditions |
| ASLargininosuccinate lyase | Often (30–79%) | In 1 condition |
| CA5Acarbonic anhydrase 5A | Often (30–79%) | In 1 condition |
| CACNA1Scalcium voltage-gated channel subunit alpha1 S | Often (30–79%) | In 1 condition |
| CSPP1centrosome and spindle pole associated protein 1 | Often (30–79%) | In 1 condition |
| HLCSholocarboxylase synthetase | Often (30–79%) | In 2 conditions |
| HMGCL3-hydroxy-3-methylglutaryl-CoA lyase | Often (30–79%) | In 1 condition |
| KIAA0586KIAA0586 | Often (30–79%) | In 2 conditions |
| NAGSN-acetylglutamate synthase | Often (30–79%) | In 1 condition |
| NKX2-1NK2 homeobox 1 | Often (30–79%) | In 1 condition |
| OXCT13-oxoacid CoA-transferase 1 | Often (30–79%) | In 2 conditions |
| PLXND1plexin D1 | Often (30–79%) | In 1 condition |
| RYR1ryanodine receptor 1 | Often (30–79%) | In 2 conditions |
| SLC25A15solute carrier family 25 member 15 | Often (30–79%) | In 1 condition |
| STING1stimulator of interferon response cGAMP interactor 1 | Often (30–79%) | In 1 condition |
| ARMC9armadillo repeat containing 9 | Sometimes (5–29%) | In 1 condition |
| ARSLarylsulfatase L | Sometimes (5–29%) | In 1 condition |
| BTDbiotinidase | Sometimes (5–29%) | In 1 condition |
| COPAcoat protein complex I subunit alpha | Sometimes (5–29%) | In 1 condition |
Show 18 more genes
| Gene | How often it is seen | Conditions |
|---|---|---|
| CSF2RAcolony stimulating factor 2 receptor subunit alpha | Sometimes (5–29%) | In 2 conditions |
| CSF2RBcolony stimulating factor 2 receptor subunit beta | Sometimes (5–29%) | In 1 condition |
| MT-CYBmitochondrially encoded cytochrome b | Sometimes (5–29%) | In 1 condition |
| NEK1NIMA related kinase 1 | Sometimes (5–29%) | In 1 condition |
| RHAGRh associated glycoprotein | Sometimes (5–29%) | In 1 condition |
| RHCERh blood group CcEe antigens | Sometimes (5–29%) | In 1 condition |
| RHDRh blood group D antigen | Sometimes (5–29%) | In 1 condition |
| SLC34A2solute carrier family 34 member 2 | Sometimes (5–29%) | In 1 condition |
| TLL1tolloid like 1 | Sometimes (5–29%) | In 1 condition |
| ACADVLacyl-CoA dehydrogenase very long chain | Rarely (1–4%) | In 2 conditions |
| ABCD4ATP binding cassette subfamily D member 4 | Not recorded | In 1 condition |
| CASRcalcium sensing receptor | Not recorded | In 1 condition |
| IGHMBP2immunoglobulin mu DNA binding protein 2 | Not recorded | In 1 condition |
| LRPPRCleucine rich pentatricopeptide repeat containing | Not recorded | In 1 condition |
| PAM16presequence translocase associated motor 16 | Not recorded | In 1 condition |
| PCCApropionyl-CoA carboxylase subunit alpha | Not recorded | In 1 condition |
| PCCBpropionyl-CoA carboxylase subunit beta | 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.
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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 2026.10.16-c6eea6bf.
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