Neurodevelopmental Disorder Gene Set

Dataset DisGeNET Gene-Disease Associations
Category disease or phenotype associations
Type disease
External Link https://www.disgenet.org/browser/0/1/0/C3280282
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Genes

29 genes associated with the disease Neurodevelopmental Disorder in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.

Symbol Name
ARHGEF2 Rho/Rac guanine nucleotide exchange factor (GEF) 2
ATN1 atrophin 1
BPTF bromodomain PHD finger transcription factor
BRAT1 BRCA1-associated ATM activator 1
DHX30 DEAH (Asp-Glu-Ala-His) box helicase 30
DOCK3 dedicator of cytokinesis 3
FOXK2 forkhead box K2
GABBR2 gamma-aminobutyric acid (GABA) B receptor, 2
GEMIN4 gem (nuclear organelle) associated protein 4
GNAO1 guanine nucleotide binding protein (G protein), alpha activating activity polypeptide O
GRIA4 glutamate receptor, ionotropic, AMPA 4
GRIN1 glutamate receptor, ionotropic, N-methyl D-aspartate 1
HECW2 HECT, C2 and WW domain containing E3 ubiquitin protein ligase 2
IRF2BPL interferon regulatory factor 2 binding protein-like
LNPK lunapark, ER junction formation factor
NACC1 nucleus accumbens associated 1, BEN and BTB (POZ) domain containing
PACS2 phosphofurin acidic cluster sorting protein 2
PLAA phospholipase A2-activating protein
PRUNE1 prune exopolyphosphatase 1
RAB11B RAB11B, member RAS oncogene family
RERE arginine-glutamic acid dipeptide (RE) repeats
SARS1 seryl-tRNA synthetase 1
SPTBN4 spectrin, beta, non-erythrocytic 4
TRAPPC6B trafficking protein particle complex 6B
UFC1 ubiquitin-fold modifier conjugating enzyme 1
VARS valyl-tRNA synthetase
WARS2 tryptophanyl tRNA synthetase 2, mitochondrial
WDR45B WD repeat domain 45B
ZSWIM6 zinc finger, SWIM-type containing 6