migraine with aura Gene Set

Dataset GAD Gene-Disease Associations
Category disease or phenotype associations
Type disease
Description A migraine characterized by migraine headache which is preceded or accompanied by a transient focal neurological phenomenon. (Human Disease Ontology, DOID_10024)
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Genes

20 genes associated with the disease migraine with aura in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

Symbol Name
ACE angiotensin I converting enzyme
ATP1A2 ATPase, Na+/K+ transporting, alpha 2 polypeptide
CACNA1A calcium channel, voltage-dependent, P/Q type, alpha 1A subunit
CACNA1E calcium channel, voltage-dependent, R type, alpha 1E subunit
CASZ1 castor zinc finger 1
DBH dopamine beta-hydroxylase (dopamine beta-monooxygenase)
DRD2 dopamine receptor D2
EDNRA endothelin receptor type A
EDNRB endothelin receptor type B
ESR1 estrogen receptor 1
FASLG Fas ligand (TNF superfamily, member 6)
GABRA5 gamma-aminobutyric acid (GABA) A receptor, alpha 5
HTR2A 5-hydroxytryptamine (serotonin) receptor 2A, G protein-coupled
HTR2C 5-hydroxytryptamine (serotonin) receptor 2C, G protein-coupled
INSR insulin receptor
KCNJ10 potassium channel, inwardly rectifying subfamily J, member 10
KCNJ9 potassium channel, inwardly rectifying subfamily J, member 9
MTHFR methylenetetrahydrofolate reductase (NAD(P)H)
SLC6A3 solute carrier family 6 (neurotransmitter transporter), member 3
SLC6A4 solute carrier family 6 (neurotransmitter transporter), member 4