absent trochlear nerve Gene Set

Dataset MPO Gene-Phenotype Associations
Category disease or phenotype associations
Type phenotype
Description absence of the fourth cranial nerve, which normally carries the motor innervation of the superior oblique muscles of the eye (Mammalian Phenotype Ontology, MP_0001064)
External Link http://www.informatics.jax.org/searches/Phat.cgi?id=MP:0001064
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3 gene mutations causing the absent trochlear nerve phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

Symbol Name
EN1 engrailed homeobox 1
NRP2 neuropilin 2
SEMA3F sema domain, immunoglobulin domain (Ig), short basic domain, secreted, (semaphorin) 3F