Conduct Disorder Gene Set

Dataset DisGeNET Gene-Disease Associations
Category disease or phenotype associations
Type disease
Description A specific developmental disorder marked by a pattern of repetitive behavior wherein the rights of others or social norms are violated. (Human Disease Ontology, DOID_12995)
External Link https://www.disgenet.org/browser/0/1/0/C0149654
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Genes

33 genes associated with the disease Conduct Disorder in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.

Symbol Name
ADAM10 ADAM metallopeptidase domain 10
ALDH2 aldehyde dehydrogenase 2 family (mitochondrial)
AR androgen receptor
ARSD arylsulfatase D
AVPR1A arginine vasopressin receptor 1A
BDNF brain-derived neurotrophic factor
BST2 bone marrow stromal cell antigen 2
C1QTNF7 C1q and tumor necrosis factor related protein 7
CAMK2A calcium/calmodulin-dependent protein kinase II alpha
COMT catechol-O-methyltransferase
DBH dopamine beta-hydroxylase (dopamine beta-monooxygenase)
DRD2 dopamine receptor D2
DRD4 dopamine receptor D4
DRD5 dopamine receptor D5
EFNA5 ephrin-A5
EXT1 exostosin glycosyltransferase 1
FGD1 FYVE, RhoGEF and PH domain containing 1
FOXK2 forkhead box K2
GABRA2 gamma-aminobutyric acid (GABA) A receptor, alpha 2
GLDC glycine dehydrogenase (decarboxylating)
HTR1B 5-hydroxytryptamine (serotonin) receptor 1B, G protein-coupled
KITLG KIT ligand
MAOA monoamine oxidase A
MAOB monoamine oxidase B
NR3C1 nuclear receptor subfamily 3, group C, member 1 (glucocorticoid receptor)
OPRD1 opioid receptor, delta 1
OSR1 odd-skipped related transciption factor 1
OXT oxytocin/neurophysin I prepropeptide
OXTR oxytocin receptor
PDE10A phosphodiesterase 10A
ROBO2 roundabout, axon guidance receptor, homolog 2 (Drosophila)
SLC6A3 solute carrier family 6 (neurotransmitter transporter), member 3
SLC6A4 solute carrier family 6 (neurotransmitter transporter), member 4