migraine with aura Gene Set

Dataset HPO Gene-Disease Associations
Category disease or phenotype associations
Type phenotype
Description A migraine characterized by migraine headache which is preceded or accompanied by a transient focal neurological phenomenon. (Human Disease Ontology, DOID_10024)
External Link http://compbio.charite.de/hpoweb/showterm?id=HP:0002077
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6 genes associated with the migraine with aura phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

Symbol Name
ATP1A2 ATPase, Na+/K+ transporting, alpha 2 polypeptide
CACNA1A calcium channel, voltage-dependent, P/Q type, alpha 1A subunit
COL4A1 collagen, type IV, alpha 1
EDNRA endothelin receptor type A
SCN1A sodium channel, voltage gated, type I alpha subunit
TNF tumor necrosis factor