migraine without aura Gene Set

Dataset GAD Gene-Disease Associations
Category disease or phenotype associations
Type disease
Description A migraine that is characterized by migraine headaches that are not accompanied by an aura. (Human Disease Ontology, DOID_12783)
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Genes

15 genes associated with the disease migraine without aura in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

Symbol Name
ATP2C2 ATPase, Ca++ transporting, type 2C, member 2
CACNA1E calcium channel, voltage-dependent, R type, alpha 1E subunit
CACNB2 calcium channel, voltage-dependent, beta 2 subunit
CLIC5 chloride intracellular channel 5
IGLL1 immunoglobulin lambda-like polypeptide 1
KCNB2 potassium channel, voltage gated Shab related subfamily B, member 2
KCNE2 potassium channel, voltage gated subfamily E regulatory beta subunit 2
KCNK12 potassium channel, two pore domain subfamily K, member 12
KCNK2 potassium channel, two pore domain subfamily K, member 2
KCNQ3 potassium channel, voltage gated KQT-like subfamily Q, member 3
KCNS3 potassium voltage-gated channel, modifier subfamily S, member 3
LDLR low density lipoprotein receptor
SCN5A sodium channel, voltage gated, type V alpha subunit
SCN9A sodium channel, voltage gated, type IX alpha subunit
TNF tumor necrosis factor