abnormal accessory olfactory bulb morphology Gene Set

Dataset MPO Gene-Phenotype Associations
Category disease or phenotype associations
Type phenotype
Description any structural anomaly of the forebrain region that coordinates sensory signaling arising from the vomeronasal organ; it is located on the dorsal-posterior portion of the main olfactory bulb, and the axons that leave the accessory olfactory bulb project to targets in the amygdala and hypothalamus (Mammalian Phenotype Ontology, MP_0009945)
External Link http://www.informatics.jax.org/searches/Phat.cgi?id=MP:0009945
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3 gene mutations causing the abnormal accessory olfactory bulb morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

Symbol Name
GNG2 guanine nucleotide binding protein (G protein), gamma 2
NAGLU N-acetylglucosaminidase, alpha
TRPC2 transient receptor potential cation channel, subfamily C, member 2, pseudogene