insomnia Gene Set

Dataset	HPO Gene-Disease Associations
Category	disease or phenotype associations
Type	phenotype
Description	Disorders characterized by impairment of the ability to initiate or maintain sleep. This may occur as a primary disorder or in association with another medical or psychiatric condition (Experimental Factor Ontology, EFO_0004698)
External Link	http://compbio.charite.de/hpoweb/showterm?id=HP:0100785
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Genes

12 genes associated with the insomnia phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

Symbol	Name
BAZ1B	bromodomain adjacent to zinc finger domain, 1B
CLIP2	CAP-GLY domain containing linker protein 2
CPOX	coproporphyrinogen oxidase
DCTN1	dynactin 1
ELN	elastin
GTF2I	general transcription factor IIi
GTF2IRD1	GTF2I repeat domain containing 1
HMBS	hydroxymethylbilane synthase
LIMK1	LIM domain kinase 1
PRNP	prion protein
RFC2	replication factor C (activator 1) 2, 40kDa
TBL2	transducin (beta)-like 2