respiratory difficulties Gene Set

Dataset HPO Gene-Disease Associations
Category disease or phenotype associations
Type phenotype
External Link http://compbio.charite.de/hpoweb/showterm?id=HP:0002880
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Genes

15 genes associated with the respiratory difficulties phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

Symbol Name
COA5 cytochrome c oxidase assembly factor 5
COX10 COX10 heme A:farnesyltransferase cytochrome c oxidase assembly factor
COX14 COX14 cytochrome c oxidase assembly factor
COX20 COX20 cytochrome c oxidase assembly factor
COX6B1 cytochrome c oxidase subunit VIb polypeptide 1 (ubiquitous)
CREBBP CREB binding protein
EDA ectodysplasin A
EFTUD2 elongation factor Tu GTP binding domain containing 2
FASTKD2 FAST kinase domains 2
PDHA1 pyruvate dehydrogenase (lipoamide) alpha 1
PET100 PET100 homolog (S. cerevisiae)
SCO2 SCO2 cytochrome c oxidase assembly protein
STAT5B signal transducer and activator of transcription 5B
STT3B STT3B, subunit of the oligosaccharyltransferase complex (catalytic)
TACO1 translational activator of mitochondrially encoded cytochrome c oxidase I