abnormal olfactory nerve morphology Gene Set

Dataset MPO Gene-Phenotype Associations
Category disease or phenotype associations
Type phenotype
Description any structural anomaly of the first cranial nerve, which conveys the sense of smell (Mammalian Phenotype Ontology, MP_0005236)
External Link http://www.informatics.jax.org/searches/Phat.cgi?id=MP:0005236
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13 gene mutations causing the abnormal olfactory nerve morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

Symbol Name
CNGA2 cyclic nucleotide gated channel alpha 2
CNTN4 contactin 4
DLX5 distal-less homeobox 5
EBF2 early B-cell factor 2
GLI3 GLI family zinc finger 3
KLF7 Kruppel-like factor 7 (ubiquitous)
LGALS1 lectin, galactoside-binding, soluble, 1
NPC1 Niemann-Pick disease, type C1
PAX6 paired box 6
SH2D3C SH2 domain containing 3C
ZEB1 zinc finger E-box binding homeobox 1
ZIC3 Zic family member 3
ZNF423 zinc finger protein 423