absent inner dynein arms Gene Set

Dataset HPO Gene-Disease Associations
Category disease or phenotype associations
Type phenotype
Description Absence of the outer dynein arms of respiratory motile cilia, which normally are situated within the peripheral microtubules of motile cilia. This feature is usually appreciated by electron microscopy. (Human Phenotype Ontology, HP_0012257)
External Link http://compbio.charite.de/hpoweb/showterm?id=HP:0012257
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Genes

4 genes associated with the absent inner dynein arms phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

Symbol Name
CCDC39 coiled-coil domain containing 39
DNAAF1 dynein, axonemal, assembly factor 1
DNAAF3 dynein, axonemal, assembly factor 3
LRRC6 leucine rich repeat containing 6