abnormal respiratory motile cilium morphology Gene Set

Dataset	HPO Gene-Disease Associations
Category	disease or phenotype associations
Type	phenotype
Description	Abnormal arrangement of the structures of the axoneme, which is the cytoskeletal structure that forms the inner core of the motile cilium and displays a canonical 9 + 2 microtubular pattern of motile cilia studded with dynein arms. (Human Phenotype Ontology, HP_0005938)
External Link	http://compbio.charite.de/hpoweb/showterm?id=HP:0005938
Similar Terms
Downloads & Tools

Genes

14 genes associated with the abnormal respiratory motile cilium morphology phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

Symbol	Name
CCDC103	coiled-coil domain containing 103
CCDC114	coiled-coil domain containing 114
CCDC39	coiled-coil domain containing 39
CCDC40	coiled-coil domain containing 40
DNAAF1	dynein, axonemal, assembly factor 1
DNAAF2	dynein, axonemal, assembly factor 2
DNAAF3	dynein, axonemal, assembly factor 3
DNAAF5	dynein, axonemal, assembly factor 5
DNAI1	dynein, axonemal, intermediate chain 1
DNAL1	dynein, axonemal, light chain 1
LRRC6	leucine rich repeat containing 6
NME8	NME/NM23 family member 8
RSPH4A	radial spoke head 4 homolog A (Chlamydomonas)
RSPH9	radial spoke head 9 homolog (Chlamydomonas)