abnormal social behavior Gene Set

Dataset HPO Gene-Disease Associations
Category disease or phenotype associations
Type phenotype
Description An abnormality of actions or reactions of a person taking place during interactions with others. (Human Phenotype Ontology, HP_0012433)
External Link http://compbio.charite.de/hpoweb/showterm?id=HP:0012433
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23 genes associated with the abnormal social behavior phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

Symbol Name
ACOX1 acyl-CoA oxidase 1, palmitoyl
ADSL adenylosuccinate lyase
ARFGEF2 ADP-ribosylation factor guanine nucleotide-exchange factor 2 (brefeldin A-inhibited)
C10ORF2 chromosome 10 open reading frame 2
CDKL5 cyclin-dependent kinase-like 5
CLP1 cleavage and polyadenylation factor I subunit 1
CNTNAP2 contactin associated protein-like 2
DEAF1 DEAF1 transcription factor
FMR1 fragile X mental retardation 1
FOXG1 forkhead box G1
GFM1 G elongation factor, mitochondrial 1
KCNT1 potassium channel, sodium activated subfamily T, member 1
KIAA2022 KIAA2022
MECP2 methyl CpG binding protein 2
MED12 mediator complex subunit 12
MEF2C myocyte enhancer factor 2C
NALCN sodium leak channel, non selective
NLGN4X neuroligin 4, X-linked
SHANK3 SH3 and multiple ankyrin repeat domains 3
SLC25A1 solute carrier family 25 (mitochondrial carrier; citrate transporter), member 1
SLC25A12 solute carrier family 25 (aspartate/glutamate carrier), member 12
SLC6A8 solute carrier family 6 (neurotransmitter transporter), member 8
ST3GAL3 ST3 beta-galactoside alpha-2,3-sialyltransferase 3