attention deficit hyperactivity disorder Gene Set

Dataset GAD Gene-Disease Associations
Category disease or phenotype associations
Type disease
Description A specific developmental disorder that is characterized by co-existence of attentional problems and hyperactivity, with each behavior occurring infrequently alone and symptoms starting before seven years of age. (Human Disease Ontology, DOID_1094)
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Genes

18 genes associated with the disease attention deficit hyperactivity disorder in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

Symbol Name
ADRA2A adrenoceptor alpha 2A
CALY calcyon neuron-specific vesicular protein
DBH dopamine beta-hydroxylase (dopamine beta-monooxygenase)
DRD1 dopamine receptor D1
DRD2 dopamine receptor D2
DRD4 dopamine receptor D4
DRD5 dopamine receptor D5
HTR1B 5-hydroxytryptamine (serotonin) receptor 1B, G protein-coupled
MAOA monoamine oxidase A
NET1 neuroepithelial cell transforming 1
NR4A2 nuclear receptor subfamily 4, group A, member 2
SLC6A2 solute carrier family 6 (neurotransmitter transporter), member 2
SLC6A3 solute carrier family 6 (neurotransmitter transporter), member 3
SLC6A4 solute carrier family 6 (neurotransmitter transporter), member 4
SNAP25 synaptosomal-associated protein, 25kDa
SYP synaptophysin
TPH1 tryptophan hydroxylase 1
TPH2 tryptophan hydroxylase 2