dynein arm defect of respiratory motile cilia Gene Set

Dataset HPO Gene-Disease Associations
Category disease or phenotype associations
Type phenotype
Description An anomaly of the dynein arms of motile cilia. This feature is usually appreciated by electron microscopy. (Human Phenotype Ontology, HP_0012255)
External Link http://compbio.charite.de/hpoweb/showterm?id=HP:0012255
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Genes

8 genes associated with the dynein arm defect of respiratory motile cilia phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

Symbol Name
CCDC114 coiled-coil domain containing 114
CCDC39 coiled-coil domain containing 39
DNAAF1 dynein, axonemal, assembly factor 1
DNAAF3 dynein, axonemal, assembly factor 3
DNAAF5 dynein, axonemal, assembly factor 5
DNAL1 dynein, axonemal, light chain 1
LRRC6 leucine rich repeat containing 6
NME8 NME/NM23 family member 8