abnormal non-rapid eye movement sleep pattern Gene Set

Dataset MPO Gene-Phenotype Associations
Category disease or phenotype associations
Type phenotype
Description any anomaly in the frequency or duration of the sleep stages characterized by distinct EEG patterns, decreased metabolic activity, slowed breathing and heart rate, and the absence of rapid eye movement and dreaming (Mammalian Phenotype Ontology, MP_0012289)
External Link http://www.informatics.jax.org/searches/Phat.cgi?id=MP:0012289
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4 gene mutations causing the abnormal non-rapid eye movement sleep pattern phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

Symbol Name
ATP1A3 ATPase, Na+/K+ transporting, alpha 3 polypeptide
CCDC7 coiled-coil domain containing 7
HCRT hypocretin (orexin) neuropeptide precursor
HCRTR2 hypocretin (orexin) receptor 2