Language Development Disorders Gene Set

Dataset HuGE Navigator Gene-Phenotype Associations
Category disease or phenotype associations
Type phenotype
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28 genes associated with the Language Development Disorders phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset.

Symbol Name
ARNT2 aryl-hydrocarbon receptor nuclear translocator 2
ATP2C2 ATPase, Ca++ transporting, type 2C, member 2
CD38 CD38 molecule
CMIP c-Maf inducing protein
CNTNAP2 contactin associated protein-like 2
COL4A2 collagen, type IV, alpha 2
CYAT1 immunoglobulin lambda light chain-like
DCDC2 doublecortin domain containing 2
DYX1C1 dyslexia susceptibility 1 candidate 1
EN2 engrailed homeobox 2
FOXP2 forkhead box P2
GAMT guanidinoacetate N-methyltransferase
GCFC2 GC-rich sequence DNA-binding factor 2
GJB2 gap junction protein, beta 2, 26kDa
GLRA1 glycine receptor, alpha 1
GLRB glycine receptor, beta
GRM7 glutamate receptor, metabotropic 7
GTF2I general transcription factor IIi
KIAA0319 KIAA0319
NDST4 N-deacetylase/N-sulfotransferase (heparan glucosaminyl) 4
NRXN1 neurexin 1
OXT oxytocin/neurophysin I prepropeptide
ROBO1 roundabout, axon guidance receptor, homolog 1 (Drosophila)
SIM1 single-minded family bHLH transcription factor 1
SLC6A5 solute carrier family 6 (neurotransmitter transporter), member 5
STX1A syntaxin 1A (brain)
WNT2 wingless-type MMTV integration site family member 2
ZNF385D zinc finger protein 385D