abnormal ciliary motility Gene Set

Dataset HPO Gene-Disease Associations
Category disease or phenotype associations
Type phenotype
Description Any anomaly of the normal motility of motile cilia. Evaluation of ciliary beat frequency and ciliary beat pattern requires high-speed videomicroscopy of freshly obtained ciliary biopsies that are maintained in culture media under controlled conditions. (Human Phenotype Ontology, HP_0012262)
External Link http://compbio.charite.de/hpoweb/showterm?id=HP:0012262
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Genes

14 genes associated with the abnormal ciliary motility 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
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)