Bulimia Nervosa Gene Set

Dataset DisGeNET Gene-Disease Associations
Category disease or phenotype associations
Type disease
Description An eating disorder that is characterized by a cycle of binge eating (BULIMIA or bingeing) followed by inappropriate acts (purging) to avert weight gain. Purging methods often include self-induced VOMITING, use of LAXATIVES or DIURETICS, excessive exercise, and FASTING. (Experimental Factor Ontology, EFO_0005204)
External Link https://www.disgenet.org/browser/0/1/0/C2267227
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Genes

68 genes associated with the disease Bulimia Nervosa in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.

Symbol Name
ABCB1 ATP-binding cassette, sub-family B (MDR/TAP), member 1
ADIPOQ adiponectin, C1Q and collagen domain containing
AGRP agouti related neuropeptide
ALDH1A1 aldehyde dehydrogenase 1 family, member A1
ATP8A2 ATPase, aminophospholipid transporter, class I, type 8A, member 2
BDNF brain-derived neurotrophic factor
BRD2 bromodomain containing 2
CCND1 cyclin D1
CHODL chondrolectin
CIT citron rho-interacting serine/threonine kinase
CLOCK clock circadian regulator
CNR1 cannabinoid receptor 1 (brain)
COMT catechol-O-methyltransferase
CTNNBIP1 catenin, beta interacting protein 1
DPP4 dipeptidyl-peptidase 4
DRD2 dopamine receptor D2
DRD4 dopamine receptor D4
DST dystonin
EHMT1 euchromatic histone-lysine N-methyltransferase 1
ESR1 estrogen receptor 1
ESR2 estrogen receptor 2 (ER beta)
FAAH fatty acid amide hydrolase
FTO fat mass and obesity associated
GCG glucagon
GGCT gamma-glutamylcyclotransferase
GH1 growth hormone 1
GHRL ghrelin/obestatin prepropeptide
GHSR growth hormone secretagogue receptor
GLP1R glucagon-like peptide 1 receptor
GPT glutamic-pyruvate transaminase (alanine aminotransferase)
HTR1A 5-hydroxytryptamine (serotonin) receptor 1A, G protein-coupled
HTR1B 5-hydroxytryptamine (serotonin) receptor 1B, G protein-coupled
HTR2A 5-hydroxytryptamine (serotonin) receptor 2A, G protein-coupled
HTR2C 5-hydroxytryptamine (serotonin) receptor 2C, G protein-coupled
HTR3A 5-hydroxytryptamine (serotonin) receptor 3A, ionotropic
HTR3B 5-hydroxytryptamine (serotonin) receptor 3B, ionotropic
IGF1 insulin-like growth factor 1 (somatomedin C)
IGF2 insulin-like growth factor 2
KRT7 keratin 7, type II
LEP leptin
MBOAT4 membrane bound O-acyltransferase domain containing 4
MC4R melanocortin 4 receptor
MCL1 myeloid cell leukemia 1
MMP9 matrix metallopeptidase 9
NKAIN3 Na+/K+ transporting ATPase interacting 3
NR3C1 nuclear receptor subfamily 3, group C, member 1 (glucocorticoid receptor)
NT5C1B 5'-nucleotidase, cytosolic IB
NTRK2 neurotrophic tyrosine kinase, receptor, type 2
OCA2 oculocutaneous albinism II
OPN1SW opsin 1 (cone pigments), short-wave-sensitive
OR2AG1 olfactory receptor, family 2, subfamily AG, member 1 (gene/pseudogene)
OXTR oxytocin receptor
PEA15 phosphoprotein enriched in astrocytes 15
PYY peptide YY
SCLY selenocysteine lyase
SHBG sex hormone-binding globulin
SLC2A1 solute carrier family 2 (facilitated glucose transporter), member 1
SLC6A3 solute carrier family 6 (neurotransmitter transporter), member 3
SLC6A4 solute carrier family 6 (neurotransmitter transporter), member 4
SNCA synuclein, alpha (non A4 component of amyloid precursor)
ST8SIA4 ST8 alpha-N-acetyl-neuraminide alpha-2,8-sialyltransferase 4
SULT1A1 sulfotransferase family, cytosolic, 1A, phenol-preferring, member 1
SYTL5 synaptotagmin-like 5
TAL1 T-cell acute lymphocytic leukemia 1
TBC1D9 TBC1 domain family, member 9 (with GRAM domain)
TPH1 tryptophan hydroxylase 1
WASF3 WAS protein family, member 3
ZGLP1 zinc finger, GATA-like protein 1