tachypnea Gene Set

Dataset HPO Gene-Disease Associations
Category disease or phenotype associations
Type phenotype
Description Very rapid breathing. (Human Phenotype Ontology, HP_0002789)
External Link http://compbio.charite.de/hpoweb/showterm?id=HP:0002789
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Genes

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

Symbol Name
ABCA3 ATP-binding cassette, sub-family A (ABC1), member 3
ABCD4 ATP-binding cassette, sub-family D (ALD), member 4
ACADVL acyl-CoA dehydrogenase, very long chain
ACTA2 actin, alpha 2, smooth muscle, aorta
AHI1 Abelson helper integration site 1
BTD biotinidase
CA5A carbonic anhydrase VA, mitochondrial
CASR calcium-sensing receptor
CEP290 centrosomal protein 290kDa
CSF2RA colony stimulating factor 2 receptor, alpha, low-affinity (granulocyte-macrophage)
HLCS holocarboxylase synthetase (biotin-(proprionyl-CoA-carboxylase (ATP-hydrolysing)) ligase)
IGHMBP2 immunoglobulin mu binding protein 2
INPP5E inositol polyphosphate-5-phosphatase, 72 kDa
LRPPRC leucine-rich pentatricopeptide repeat containing
OXCT1 3-oxoacid CoA transferase 1
PCCA propionyl CoA carboxylase, alpha polypeptide
PCCB propionyl CoA carboxylase, beta polypeptide
SFTPB surfactant protein B
SFTPC surfactant protein C
TMEM216 transmembrane protein 216