abnormal respiratory motile cilium physiology Gene Set

Dataset	HPO Gene-Disease Associations
Category	disease or phenotype associations
Type	phenotype
Description	Any functional anomaly of the respiratory motile cilia. (Human Phenotype Ontology, HP_0012261)
External Link	http://compbio.charite.de/hpoweb/showterm?id=HP:0012261
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Genes

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

Symbol	Name
ARMC4	armadillo repeat containing 4
C21ORF59	chromosome 21 open reading frame 59
CCDC103	coiled-coil domain containing 103
CCDC114	coiled-coil domain containing 114
CCDC39	coiled-coil domain containing 39
CCDC65	coiled-coil domain containing 65
DNAAF3	dynein, axonemal, assembly factor 3
DNAAF5	dynein, axonemal, assembly factor 5
DNAH11	dynein, axonemal, heavy chain 11
DNAI1	dynein, axonemal, intermediate chain 1
DNAL1	dynein, axonemal, light chain 1
DYX1C1	dyslexia susceptibility 1 candidate 1
HYDIN	HYDIN, axonemal central pair apparatus protein
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)
SPAG1	sperm associated antigen 1
ZMYND10	zinc finger, MYND-type containing 10