abnormal mucociliary clearance Gene Set

Dataset MPO Gene-Phenotype Associations
Category disease or phenotype associations
Type phenotype
Description anomaly in the mechanism that removes mucus and other foreign particles and microorganisms from the lungs by directed ciliary movement and secretory activity of the tracheobronchial submucosal glands (Mammalian Phenotype Ontology, MP_0001947)
External Link http://www.informatics.jax.org/searches/Phat.cgi?id=MP:0001947
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9 gene mutations causing the abnormal mucociliary clearance phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

Symbol Name
AK7 adenylate kinase 7
CBY1 chibby homolog 1 (Drosophila)
DPCD deleted in primary ciliary dyskinesia homolog (mouse)
HYDIN HYDIN, axonemal central pair apparatus protein
KIF27 kinesin family member 27
MUC5B mucin 5B, oligomeric mucus/gel-forming
NME5 NME/NM23 family member 5
TEKT2 tektin 2 (testicular)
TTLL1 tubulin tyrosine ligase-like family member 1