Child Development Deviations Gene Set

Dataset DisGeNET Gene-Disease Associations
Category disease or phenotype associations
Type disease
External Link https://www.disgenet.org/browser/0/1/0/C0085996
Similar Terms
Downloads & Tools

Genes

30 genes associated with the disease Child Development Deviations in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.

Symbol Name
ARFGAP1 ADP-ribosylation factor GTPase activating protein 1
AS3MT arsenite methyltransferase
CAMKMT calmodulin-lysine N-methyltransferase
CBL Cbl proto-oncogene, E3 ubiquitin protein ligase
CHD4 chromodomain helicase DNA binding protein 4
CHRNA4 cholinergic receptor, nicotinic, alpha 4 (neuronal)
CNTN4 contactin 4
DOCK8 dedicator of cytokinesis 8
DRD2 dopamine receptor D2
KCNQ2 potassium channel, voltage gated KQT-like subfamily Q, member 2
KCNT1 potassium channel, sodium activated subfamily T, member 1
KIF1A kinesin family member 1A
LRP2 low density lipoprotein receptor-related protein 2
MAPK3 mitogen-activated protein kinase 3
MECP2 methyl CpG binding protein 2
MSL3 male-specific lethal 3 homolog (Drosophila)
NANS N-acetylneuraminic acid synthase
NTRK2 neurotrophic tyrosine kinase, receptor, type 2
PDC phosducin
PMP22 peripheral myelin protein 22
PNKP polynucleotide kinase 3'-phosphatase
PTEN phosphatase and tensin homolog
SHANK3 SH3 and multiple ankyrin repeat domains 3
SLC2A1 solute carrier family 2 (facilitated glucose transporter), member 1
SLC33A1 solute carrier family 33 (acetyl-CoA transporter), member 1
SLC4A4 solute carrier family 4 (sodium bicarbonate cotransporter), member 4
SLC6A8 solute carrier family 6 (neurotransmitter transporter), member 8
STAMBP STAM binding protein
TBCD tubulin folding cofactor D
WDFY4 WDFY family member 4