abnormal oculomotor nerve morphology Gene Set

Dataset	MPO Gene-Phenotype Associations
Category	disease or phenotype associations
Type	phenotype
Description	any structural anomaly of the third cranial nerve, which normally sends motor fibers to the levator muscles of the eyelid and to the superior rectus, inferior rectus, and inferior oblique muscles of the eye; and also sends parasympathetic efferents to the muscles controlling pupillary constriction and accommodation (Mammalian Phenotype Ontology, MP_0001061)
External Link	http://www.informatics.jax.org/searches/Phat.cgi?id=MP:0001061
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Genes

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

Symbol	Name
EFNB1	ephrin-B1
EN1	engrailed homeobox 1
NR6A1	nuclear receptor subfamily 6, group A, member 1
NRP2	neuropilin 2
OTX2	orthodenticle homeobox 2
PHOX2A	paired-like homeobox 2a
SEMA3F	sema domain, immunoglobulin domain (Ig), short basic domain, secreted, (semaphorin) 3F
TFAP2A	transcription factor AP-2 alpha (activating enhancer binding protein 2 alpha)
TUBB3	tubulin, beta 3 class III