Migraine Gene Set

Dataset DISEASES Curated Gene-Disease Association Evidence Scores 2025
Category disease or phenotype associations
Type disease
Description A brain disease that is characterized by moderate to severe headaches, nausea, extreme sensitivity to light and sound and intense unilaterial throbbing or pulsing. (Human Disease Ontology, DOID_6364)
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Genes

20 genes involed in the disease Migraine from the DISEASES Curated Gene-Disease Association Evidence Scores 2025 dataset.

Symbol Name Standardized Value
PHACTR1 phosphatase and actin regulator 1 5.0
ATP1A2 ATPase, Na+/K+ transporting, alpha 2 polypeptide 5.0
PRDM16 PR domain containing 16 5.0
MEF2D myocyte enhancer factor 2D 5.0
CACNA1A calcium channel, voltage-dependent, P/Q type, alpha 1A subunit 5.0
RNF213 ring finger protein 213 5.0
PRRT2 proline-rich transmembrane protein 2 5.0
MPPED2 metallophosphoesterase domain containing 2 5.0
CARF calcium responsive transcription factor 5.0
PLCE1 phospholipase C, epsilon 1 5.0
SLC24A3 solute carrier family 24 (sodium/potassium/calcium exchanger), member 3 5.0
SUGCT succinyl-CoA:glutarate-CoA transferase 5.0
IGSF9B immunoglobulin superfamily, member 9B 5.0
ASTN2 astrotactin 2 5.0
SCN1A sodium channel, voltage gated, type I alpha subunit 5.0
NRP1 neuropilin 1 5.0
CFDP1 craniofacial development protein 1 5.0
HPSE2 heparanase 2 (inactive) 5.0
KCNK5 potassium channel, two pore domain subfamily K, member 5 5.0
YAP1 Yes-associated protein 1 5.0