asperger syndrome Gene Set

Dataset GWASdb SNP-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 http://jjwanglab.org/gwasdb/gwasdb2/gwasdb2/go_trait/DOID:0050432
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Genes

24 genes associated with the disease asperger syndrome in GWAS and other genetic association datasets from the GWASdb SNP-Disease Associations dataset.

Symbol Name Standardized Value
NTM neurotrimin 1.14463
FHIT fragile histidine triad 1.07599
RASGRP4 RAS guanyl releasing protein 4 1.04846
SLTM SAFB-like, transcription modulator 1.00407
TTI1 TELO2 interacting protein 1 0.88034
FAM171A1 family with sequence similarity 171, member A1 0.88034
SKAP1 src kinase associated phosphoprotein 1 0.88034
KLHDC10 kelch domain containing 10 0.831584
TSHZ1 teashirt zinc finger homeobox 1 0.794247
GANC glucosidase, alpha; neutral C 0.764084
THBS4 thrombospondin 4 0.69773
MYO5B myosin VB 0.681983
JPH4 junctophilin 4 0.668836
BCAS3 breast carcinoma amplified sequence 3 0.634147
APOBEC4 apolipoprotein B mRNA editing enzyme, catalytic polypeptide-like 4 (putative) 0.625701
RNF111 ring finger protein 111 0.618434
TMEM132B transmembrane protein 132B 0.615118
RIMS2 regulating synaptic membrane exocytosis 2 0.591358
GFRA1 GDNF family receptor alpha 1 0.57934
CEP78 centrosomal protein 78kDa 0.574821
RGL1 ral guanine nucleotide dissociation stimulator-like 1 0.566629
ADGB androglobin 0.557222
TGFB1 transforming growth factor, beta 1 0.542589
ATMIN ATM interactor 0.524983