hyperventilation Gene Set

Dataset HPO Gene-Disease Associations
Category disease or phenotype associations
Type phenotype
Description Hyperventilation refers to an increased pulmonary ventilation rate that is faster than necessary for the exchange of gases. Hyperventilation can result from increased frequency of breathing, an increased tidal volume, or both, and leads to an excess intake of oxygen and the blowing off of carbon dioxide. (Human Phenotype Ontology, HP_0002883)
External Link http://compbio.charite.de/hpoweb/showterm?id=HP:0002883
Similar Terms
Downloads & Tools

Genes

8 genes associated with the hyperventilation phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

Symbol Name
C5ORF42 chromosome 5 open reading frame 42
CDKL5 cyclin-dependent kinase-like 5
FBP1 fructose-1,6-bisphosphatase 1
HLCS holocarboxylase synthetase (biotin-(proprionyl-CoA-carboxylase (ATP-hydrolysing)) ligase)
MECP2 methyl CpG binding protein 2
NRXN1 neurexin 1
SUCLG1 succinate-CoA ligase, alpha subunit
TCF4 transcription factor 4