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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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