abnormal respiratory motile cilium morphology Gene Set

Dataset MPO Gene-Phenotype 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://www.informatics.jax.org/searches/Phat.cgi?id=MP:0011050
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12 gene mutations causing the abnormal respiratory motile cilium morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

Symbol Name
AK7 adenylate kinase 7
ARMC4 armadillo repeat containing 4
CBY1 chibby homolog 1 (Drosophila)
CRB3 crumbs family member 3
DNAH5 dynein, axonemal, heavy chain 5
FOXJ1 forkhead box J1
HYDIN HYDIN, axonemal central pair apparatus protein
KIF19 kinesin family member 19
MNS1 meiosis-specific nuclear structural 1
TEKT2 tektin 2 (testicular)
TTLL1 tubulin tyrosine ligase-like family member 1
ULK4 unc-51 like kinase 4