Asperger Syndrome Gene Set

Dataset DisGeNET Gene-Disease Associations
Category disease or phenotype associations
Type disease
Description An autism spectrum disorder that is characterized by significant difficulties in social interaction, along with restricted and repetitive patterns of behavior and interests. It differs from other autism spectrum disorders by its relative preservation of linguistic and cognitive development. (Human Disease Ontology, DOID_0050432)
External Link https://www.disgenet.org/browser/0/1/0/C0236792
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Genes

16 genes associated with the disease Asperger Syndrome in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.

Symbol Name
ARSD arylsulfatase D
BDNF brain-derived neurotrophic factor
CTSL cathepsin L
DISC1 disrupted in schizophrenia 1
GABRB3 gamma-aminobutyric acid (GABA) A receptor, beta 3
MECP2 methyl CpG binding protein 2
MTHFR methylenetetrahydrofolate reductase (NAD(P)H)
NLN neurolysin (metallopeptidase M3 family)
NOS1 nitric oxide synthase 1 (neuronal)
NOS2 nitric oxide synthase 2, inducible
NRXN1 neurexin 1
OXTR oxytocin receptor
SHANK3 SH3 and multiple ankyrin repeat domains 3
SLC6A4 solute carrier family 6 (neurotransmitter transporter), member 4
TSNAX translin-associated factor X
VIP vasoactive intestinal peptide