Reading Disabilities Gene Set
Genes
21 genes associated with the disease Reading Disabilities in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
| Symbol |
Name |
|
ACOT13
|
acyl-CoA thioesterase 13
|
|
DCDC2
|
doublecortin domain containing 2
|
|
DNAAF4
|
dynein axonemal assembly factor 4
|
|
DRD1
|
dopamine receptor D1
|
|
FOXP2
|
forkhead box P2
|
|
HLA-DRB1
|
major histocompatibility complex, class II, DR beta 1
|
|
KIAA0319
|
KIAA0319
|
|
KIAA0319L
|
KIAA0319-like
|
|
MOG
|
myelin oligodendrocyte glycoprotein
|
|
OTX1
|
orthodenticle homeobox 1
|
|
PRTG
|
protogenin
|
|
RBM45
|
RNA binding motif protein 45
|
|
ROBO1
|
roundabout, axon guidance receptor, homolog 1 (Drosophila)
|
|
SEMA4F
|
sema domain, immunoglobulin domain (Ig), transmembrane domain (TM) and short cytoplasmic domain, (semaphorin) 4F
|
|
SHC2
|
SHC (Src homology 2 domain containing) transforming protein 2
|
|
SLC6A3
|
solute carrier family 6 (neurotransmitter transporter), member 3
|
|
TDP2
|
tyrosyl-DNA phosphodiesterase 2
|
|
TRD
|
T cell receptor delta locus
|
|
WASF1
|
WAS protein family, member 1
|
|
WASF3
|
WAS protein family, member 3
|
|
ZNF385D
|
zinc finger protein 385D
|
