abnormal maxillary nerve morphology Gene Set

Dataset MPO Gene-Phenotype Associations
Category disease or phenotype associations
Type phenotype
Description any structural anomaly of the sensory nerve subdivision of the trigeminal nerve that transmits sensory information from the palate, upper teeth and gingiva, the skin between the palpebral fissure and the mouth, and from the nasal cavity and maxillary sinuses (Mammalian Phenotype Ontology, MP_0009799)
External Link http://www.informatics.jax.org/searches/Phat.cgi?id=MP:0009799
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Genes

2 gene mutations causing the abnormal maxillary nerve morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

Symbol Name
CYP26A1 cytochrome P450, family 26, subfamily A, polypeptide 1
MEGF8 multiple EGF-like-domains 8