migraine Gene Set

Dataset DISEASES Experimental Gene-Disease Assocation Evidence Scores
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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12 genes associated with the disease migraine in GWAS datasets from the DISEASES Experimental Gene-Disease Assocation Evidence Scores dataset.

Symbol Name Standardized Value
TRPM8 transient receptor potential cation channel, subfamily M, member 8 0.894262
CPQ carboxypeptidase Q 0.790827
MEF2D myocyte enhancer factor 2D 0.738873
TGFBR2 transforming growth factor, beta receptor II (70/80kDa) 0.63207
PRDM16 PR domain containing 16 0.572184
PHACTR1 phosphatase and actin regulator 1 0.464771
ASTN2 astrotactin 2 0.449873
UFL1 UFM1-specific ligase 1 0.429338
MMP17 matrix metallopeptidase 17 (membrane-inserted) 0.311576
MARCH4 membrane-associated ring finger (C3HC4) 4, E3 ubiquitin protein ligase 0.256228
IGLL1 immunoglobulin lambda-like polypeptide 1 0.052255
INA internexin neuronal intermediate filament protein, alpha 0.043246