|Dataset||MPO Gene-Phenotype Associations|
|Category||disease or phenotype associations|
|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)|
|Downloads & Tools|
3 gene mutations causing the abnormal accessory olfactory bulb morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.