abnormal rapid eye movement (rem) sleep Gene Set

Dataset HPO Gene-Disease Associations
Category disease or phenotype associations
Type phenotype
Description Abnormality of REM sleep. Phases of REM sleep are characterized by desynchronized EEG patterns, increases in heart rate and blood pressure, sympathetic activation, and a profound loss of muscle tonus except for the eye and middle-ear muscles. There are then phases of rapid eye movements. (Human Phenotype Ontology, HP_0002494)
External Link http://compbio.charite.de/hpoweb/showterm?id=HP:0002494
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Genes

1 genes associated with the abnormal rapid eye movement (rem) sleep phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

Symbol Name
HCRT hypocretin (orexin) neuropeptide precursor