|Dataset||MPO Gene-Phenotype Associations|
|Category||disease or phenotype associations|
|Description||increased incidence or duration of the sleep stage in which dreams occur and the body undergoes marked changes including rapid eye movement, loss of reflexes, and increased pulse rate and brain activity (Mammalian Phenotype Ontology, MP_0012287)|
|Downloads & Tools|
1 gene mutations causing the increased frequency of paradoxical sleep phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
|HCRT||hypocretin (orexin) neuropeptide precursor|