Minimal Brain Dysfunction Gene Set

Dataset DisGeNET Gene-Disease Associations
Category disease or phenotype associations
Type disease
External Link https://www.disgenet.org/browser/0/1/0/C1321905
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Genes

22 genes associated with the disease Minimal Brain Dysfunction in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.

Symbol Name
ADGRL3 adhesion G protein-coupled receptor L3
AS3MT arsenite methyltransferase
CALY calcyon neuron-specific vesicular protein
CHRNA4 cholinergic receptor, nicotinic, alpha 4 (neuronal)
CHRNB2 cholinergic receptor, nicotinic, beta 2 (neuronal)
CIC capicua transcriptional repressor
CNR1 cannabinoid receptor 1 (brain)
COMT catechol-O-methyltransferase
DRD2 dopamine receptor D2
DRD4 dopamine receptor D4
DRD5 dopamine receptor D5
FGD1 FYVE, RhoGEF and PH domain containing 1
GIT1 G protein-coupled receptor kinase interacting ArfGAP 1
GRM1 glutamate receptor, metabotropic 1
GRM5 glutamate receptor, metabotropic 5
GRM7 glutamate receptor, metabotropic 7
GRM8 glutamate receptor, metabotropic 8
PTPRD protein tyrosine phosphatase, receptor type, D
SLC6A3 solute carrier family 6 (neurotransmitter transporter), member 3
STS steroid sulfatase (microsomal), isozyme S
TACR1 tachykinin receptor 1
TPH2 tryptophan hydroxylase 2