pervasive developmental disorder Gene Set

Dataset DISEASES Experimental Gene-Disease Assocation Evidence Scores
Category disease or phenotype associations
Type disease
Description A developmental disorder of mental health that refers to a group of five disorders characterized by impairments in socialization and communication, as well as restricted interests and repetitive behaviors. (Human Disease Ontology, DOID_0060040)
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Genes

26 genes associated with the disease pervasive developmental 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
SYT17 synaptotagmin XVII 0.368757
TAF1C TATA box binding protein (TBP)-associated factor, RNA polymerase I, C, 110kDa 0.345945
DMD dystrophin 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
RHOXF1 Rhox homeobox family, member 1 0.256228
ADGRL2 adhesion G protein-coupled receptor L2 0.256228
RGMB repulsive guidance molecule family member b 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
FEZF2 FEZ family zinc finger 2 0.15771
FHIT fragile histidine triad 0.126165
RASGRP4 RAS guanyl releasing protein 4 0.100789
PACRG PARK2 co-regulated 0.080593
CDH22 cadherin 22, type 2 0.080593
LRRC1 leucine rich repeat containing 1 0.080593
CCDC64 coiled-coil domain containing 64 0.080593
MAP7 microtubule-associated protein 7 0.064973
SLTM SAFB-like, transcription modulator 0.064973
MARCKS myristoylated alanine-rich protein kinase C substrate 0.052255
GRIK1 glutamate receptor, ionotropic, kainate 1 0.052255
PDZD7 PDZ domain containing 7 0.052255
CTNNA3 catenin (cadherin-associated protein), alpha 3 0.043246