abnormal olfactory neuron innervation pattern Gene Set

Dataset MPO Gene-Phenotype Associations
Category disease or phenotype associations
Type phenotype
Description any changes in the placement, morphology or number of axons from olfactory neurons to an effector tissue or to olfactory glomeruli or olfactory bulb (Mammalian Phenotype Ontology, MP_0012014)
External Link http://www.informatics.jax.org/searches/Phat.cgi?id=MP:0012014
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Genes

8 gene mutations causing the abnormal olfactory neuron innervation pattern phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

Symbol Name
CHL1 cell adhesion molecule L1-like
EBF2 early B-cell factor 2
KLF7 Kruppel-like factor 7 (ubiquitous)
NRP2 neuropilin 2
OR10A2 olfactory receptor, family 10, subfamily A, member 2
OR10A4 olfactory receptor, family 10, subfamily A, member 4
OR10A5 olfactory receptor, family 10, subfamily A, member 5
OR8A1 olfactory receptor, family 8, subfamily A, member 1