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