conduct disorder Gene Set

Dataset DISEASES Experimental Gene-Disease Assocation Evidence Scores
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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Genes

13 genes associated with the disease conduct disorder in GWAS datasets from the DISEASES Experimental Gene-Disease Assocation Evidence Scores dataset.

Symbol Name Standardized Value
C1QTNF7 C1q and tumor necrosis factor related protein 7 0.58494
FAT3 FAT atypical cadherin 3 0.52461
RBM26 RNA binding motif protein 26 0.52461
PDE10A phosphodiesterase 10A 0.256228
ARHGAP22 Rho GTPase activating protein 22 0.197766
SELPLG selectin P ligand 0.15771
TOX2 TOX high mobility group box family member 2 0.080593
ERCC4 excision repair cross-complementation group 4 0.080593
ZNF330 zinc finger protein 330 0.064973
SLC7A2 solute carrier family 7 (cationic amino acid transporter, y+ system), member 2 0.064973
GATAD2B GATA zinc finger domain containing 2B 0.052255
CC2D2A coiled-coil and C2 domain containing 2A 0.052255
NBAS neuroblastoma amplified sequence 0.052255
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