abnormal trochlear nerve morphology Gene Set

Dataset MPO Gene-Phenotype Associations
Category disease or phenotype associations
Type phenotype
Description any structural anomaly of the fourth cranial nerve, which normally carries the motor innervation of the superior oblique muscles of the eye (Mammalian Phenotype Ontology, MP_0001063)
External Link http://www.informatics.jax.org/searches/Phat.cgi?id=MP:0001063
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8 gene mutations causing the abnormal trochlear nerve morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

Symbol Name
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
TUBB3 tubulin, beta 3 class III
UNC5C unc-5 homolog C (C. elegans)