abnormal paranasal sinus morphology Gene Set

Dataset MPO Gene-Phenotype Associations
Category disease or phenotype associations
Type phenotype
Description any structural anomaly of the paired air-filled cavities surrounded by the bones of the face that are lined by mucous membranes and are continuous with the nasal cavity (Mammalian Phenotype Ontology, MP_0002240)
External Link http://www.informatics.jax.org/searches/Phat.cgi?id=MP:0002240
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6 gene mutations causing the abnormal paranasal sinus morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

Symbol Name
ALDH1A3 aldehyde dehydrogenase 1 family, member A3
ANKH ANKH inorganic pyrophosphate transport regulator
CFTR cystic fibrosis transmembrane conductance regulator (ATP-binding cassette sub-family C, member 7)
KIF27 kinesin family member 27
NME5 NME/NM23 family member 5
ULK4 unc-51 like kinase 4