Specific Language Impairment Gene Set

Dataset DisGeNET Gene-Disease Associations
Category disease or phenotype associations
Type disease
External Link https://www.disgenet.org/browser/0/1/0/C0454651
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Genes

32 genes associated with the disease Specific Language Impairment in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.

Symbol Name
ARHGEF39 Rho guanine nucleotide exchange factor (GEF) 39
ATP2C2 ATPase, Ca++ transporting, type 2C, member 2
BDNF brain-derived neurotrophic factor
BMP1 bone morphogenetic protein 1
C4ORF3 chromosome 4 open reading frame 3
CALM1 calmodulin 1 (phosphorylase kinase, delta)
CALM2 calmodulin 2 (phosphorylase kinase, delta)
CALM3 calmodulin 3 (phosphorylase kinase, delta)
CAMKMT calmodulin-lysine N-methyltransferase
CASK calcium/calmodulin-dependent serine protein kinase (MAGUK family)
CCDC136 coiled-coil domain containing 136
CMIP c-Maf inducing protein
CNTNAP2 contactin associated protein-like 2
DLD dihydrolipoamide dehydrogenase
EBPL emopamil binding protein-like
ELK3 ELK3, ETS-domain protein (SRF accessory protein 2)
FOXP1 forkhead box P1
FOXP2 forkhead box P2
HLCS holocarboxylase synthetase (biotin-(proprionyl-CoA-carboxylase (ATP-hydrolysing)) ligase)
IL13 interleukin 13
INIP INTS3 and NABP interacting protein
KRIT1 KRIT1, ankyrin repeat containing
NAGPA N-acetylglucosamine-1-phosphodiester alpha-N-acetylglucosaminidase
NFXL1 nuclear transcription factor, X-box binding-like 1
NOP9 NOP9 nucleolar protein
NRXN1 neurexin 1
RBFOX2 RNA binding protein, fox-1 homolog (C. elegans) 2
SHC2 SHC (Src homology 2 domain containing) transforming protein 2
SYN1 synapsin I
TM4SF20 transmembrane 4 L six family member 20
UBR4 ubiquitin protein ligase E3 component n-recognin 4
ZNF277 zinc finger protein 277