Executive 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/C2748208
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Genes

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

Symbol Name
ANKK1 ankyrin repeat and kinase domain containing 1
APOE apolipoprotein E
ARSD arylsulfatase D
BDNF brain-derived neurotrophic factor
CACNA1C calcium channel, voltage-dependent, L type, alpha 1C subunit
CHD2 chromodomain helicase DNA binding protein 2
CHD7 chromodomain helicase DNA binding protein 7
CHD8 chromodomain helicase DNA binding protein 8
COMT catechol-O-methyltransferase
CSF1R colony stimulating factor 1 receptor
CXCL8 chemokine (C-X-C motif) ligand 8
DRD2 dopamine receptor D2
DRD4 dopamine receptor D4
EBPL emopamil binding protein-like
ELK3 ELK3, ETS-domain protein (SRF accessory protein 2)
FMR1 fragile X mental retardation 1
ICAM1 intercellular adhesion molecule 1
MCIDAS multiciliate differentiation and DNA synthesis associated cell cycle protein
NGF nerve growth factor (beta polypeptide)
PNN pinin, desmosome associated protein
PSEN2 presenilin 2
SFXN1 sideroflexin 1
SGCA sarcoglycan, alpha (50kDa dystrophin-associated glycoprotein)
SLC6A3 solute carrier family 6 (neurotransmitter transporter), member 3
SLC6A4 solute carrier family 6 (neurotransmitter transporter), member 4
SNCA synuclein, alpha (non A4 component of amyloid precursor)
SPG11 spastic paraplegia 11 (autosomal recessive)
SRPX sushi-repeat containing protein, X-linked
STH saitohin
TOR1A torsin family 1, member A (torsin A)
TPSG1 tryptase gamma 1
XPR1 xenotropic and polytropic retrovirus receptor 1
ZBP1 Z-DNA binding protein 1