conduct disorder Gene Set

Dataset GAD 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)
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16 genes associated with the disease conduct disorder in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

Symbol Name
ARHGAP22 Rho GTPase activating protein 22
C1QTNF7 C1q and tumor necrosis factor related protein 7
CC2D2A coiled-coil and C2 domain containing 2A
ERCC4 excision repair cross-complementation group 4
LOC343052 immunoglobulin superfamily, DCC subclass, member 3 pseudogene
MFHAS1 malignant fibrous histiocytoma amplified sequence 1
NBAS neuroblastoma amplified sequence
PDE10A phosphodiesterase 10A
PPM1K protein phosphatase, Mg2+/Mn2+ dependent, 1K
RBFOX1 RNA binding protein, fox-1 homolog (C. elegans) 1
RIT1 Ras-like without CAAX 1
SELPLG selectin P ligand
SLC6A1 solute carrier family 6 (neurotransmitter transporter), member 1
TOX2 TOX high mobility group box family member 2
ZBTB16 zinc finger and BTB domain containing 16
ZNF330 zinc finger protein 330