anorexia nervosa Gene Set

Dataset	GAD Gene-Disease Associations
Category	disease or phenotype associations
Type	disease
Description	An eating disorder characterized by refusal to maintain a healthy body weight, and an obsessive fear of gaining weight due to a distorted self image. (Human Disease Ontology, DOID_8689)
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Genes

17 genes associated with the disease anorexia nervosa in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

Symbol	Name
AGRP	agouti related neuropeptide
AKAP6	A kinase (PRKA) anchor protein 6
COMT	catechol-O-methyltransferase
DRD2	dopamine receptor D2
ESR2	estrogen receptor 2 (ER beta)
FAM155A	family with sequence similarity 155, member A
HTR2A	5-hydroxytryptamine (serotonin) receptor 2A, G protein-coupled
KCNK3	potassium channel, two pore domain subfamily K, member 3
KCNN3	potassium channel, calcium activated intermediate/small conductance subfamily N alpha, member 3
LRP2	low density lipoprotein receptor-related protein 2
NTNG1	netrin G1
SLC6A2	solute carrier family 6 (neurotransmitter transporter), member 2
SLC6A4	solute carrier family 6 (neurotransmitter transporter), member 4
SPATA17	spermatogenesis associated 17
TNF	tumor necrosis factor
VGLL4	vestigial-like family member 4
ZNF804B	zinc finger protein 804B