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