abnormal internal nares morphology Gene Set

Dataset MPO Gene-Phenotype Associations
Category disease or phenotype associations
Type phenotype
Description any structural anomaly of the portion of the opening of the nasal cavity into the nasal pharynx (Mammalian Phenotype Ontology, MP_0002236)
External Link http://www.informatics.jax.org/searches/Phat.cgi?id=MP:0002236
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8 gene mutations causing the abnormal internal nares morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

Symbol Name
AK7 adenylate kinase 7
ALDH1A3 aldehyde dehydrogenase 1 family, member A3
CHD7 chromodomain helicase DNA binding protein 7
DPCD deleted in primary ciliary dyskinesia homolog (mouse)
KIF27 kinesin family member 27
NME5 NME/NM23 family member 5
TBX22 T-box 22
ULK4 unc-51 like kinase 4