abnormal ophthalmic 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 orbit and its contents, the nasal cavity and the skin of the nose and forehead (Mammalian Phenotype Ontology, MP_0009798)
External Link http://www.informatics.jax.org/searches/Phat.cgi?id=MP:0009798
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Genes

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

Symbol Name
CYP26A1 cytochrome P450, family 26, subfamily A, polypeptide 1
ERBB3 erb-b2 receptor tyrosine kinase 3
MEGF8 multiple EGF-like-domains 8
SEMA3A sema domain, immunoglobulin domain (Ig), short basic domain, secreted, (semaphorin) 3A