Conduct Disorder Gene Set

Dataset dbGAP Gene-Trait Associations
Category disease or phenotype associations
Type trait
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 trait Conduct Disorder in GWAS and other genetic association datasets from the dbGAP Gene-Trait Associations dataset.

Symbol Name Standardized Value
C1QTNF7 C1q and tumor necrosis factor related protein 7 0.820059
PDE10A phosphodiesterase 10A 0.50084
ARHGAP22 Rho GTPase activating protein 22 0.443956
SELPLG selectin P ligand 0.406869
RBFOX1 RNA binding protein, fox-1 homolog (C. elegans) 1 0.406869
SLC6A1 solute carrier family 6 (neurotransmitter transporter), member 1 0.33862
TOX2 TOX high mobility group box family member 2 0.33862
MFHAS1 malignant fibrous histiocytoma amplified sequence 1 0.33862
ERCC4 excision repair cross-complementation group 4 0.33862
PPM1K protein phosphatase, Mg2+/Mn2+ dependent, 1K 0.323533
ZNF330 zinc finger protein 330 0.323533
RIT1 Ras-like without CAAX 1 0.323533
CC2D2A coiled-coil and C2 domain containing 2A 0.310838
NBAS neuroblastoma amplified sequence 0.310838
LOC343052 immunoglobulin superfamily, DCC subclass, member 3 pseudogene 0.310838
ZBTB16 zinc finger and BTB domain containing 16 0.29992