autistic disorder Gene Set

Dataset DISEASES Experimental Gene-Disease Assocation Evidence Scores
Category disease or phenotype associations
Type disease
Description An autism spectrum disorder that is characterized by symptoms across all three symptom domains (communication, social, restricted repetitive interests and behaviors), delayed language development, and symptom onset prior to age 3 years. (Human Disease Ontology, DOID_12849)
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18 genes associated with the disease autistic disorder in GWAS datasets from the DISEASES Experimental Gene-Disease Assocation Evidence Scores dataset.

Symbol Name Standardized Value
MACROD2 MACRO domain containing 2 0.449873
TAF1C TATA box binding protein (TBP)-associated factor, RNA polymerase I, C, 110kDa 0.345945
TAS2R1 taste receptor, type 2, member 1 0.345945
PARD3B par-3 family cell polarity regulator beta 0.327313
SGCD sarcoglycan, delta (35kDa dystrophin-associated glycoprotein) 0.274608
RGMB repulsive guidance molecule family member b 0.256228
ADGRL2 adhesion G protein-coupled receptor L2 0.256228
JARID2 jumonji, AT rich interactive domain 2 0.197766
PPP2R5C protein phosphatase 2, regulatory subunit B', gamma 0.15771
NTM neurotrimin 0.15771
FHIT fragile histidine triad 0.126165
RASGRP4 RAS guanyl releasing protein 4 0.100789
PACRG PARK2 co-regulated 0.080593
SLTM SAFB-like, transcription modulator 0.064973
CTNNA3 catenin (cadherin-associated protein), alpha 3 0.064973
MAP7 microtubule-associated protein 7 0.064973
GRIK1 glutamate receptor, ionotropic, kainate 1 0.052255
MARCKS myristoylated alanine-rich protein kinase C substrate 0.052255