narcolepsy Gene Set

Dataset MPO Gene-Phenotype Associations
Category disease or phenotype associations
Type phenotype
Description A sleep disorder that involves an excessive urge to sleep at inappropriate times, such as while at work. (Human Disease Ontology, DOID_8986)
External Link http://www.informatics.jax.org/searches/Phat.cgi?id=MP:0005279
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Genes

3 gene mutations causing the narcolepsy phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

Symbol Name
EBF2 early B-cell factor 2
HCRT hypocretin (orexin) neuropeptide precursor
HCRTR2 hypocretin (orexin) receptor 2