Familial Hemiplegic Migraine Gene Set

Dataset DisGeNET Gene-Disease Associations
Category disease or phenotype associations
Type disease
Description A migraine with aura that is characterized by temporary numbness or weakness, often affecting one side of the body (hemiparesis). Additional features of an aura can include difficulty with speech, confusion, and drowsiness. (Human Disease Ontology, DOID_0060178)
External Link https://www.disgenet.org/browser/0/1/0/C0338484
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Genes

23 genes associated with the disease Familial Hemiplegic Migraine in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.

Symbol Name
ATP1A2 ATPase, Na+/K+ transporting, alpha 2 polypeptide
ATP1A4 ATPase, Na+/K+ transporting, alpha 4 polypeptide
CACNA1A calcium channel, voltage-dependent, P/Q type, alpha 1A subunit
CACNA1C calcium channel, voltage-dependent, L type, alpha 1C subunit
CALCA calcitonin-related polypeptide alpha
COL4A1 collagen, type IV, alpha 1
COL4A2 collagen, type IV, alpha 2
CSAD cysteine sulfinic acid decarboxylase
IL1A interleukin 1, alpha
IL1B interleukin 1, beta
IL1RN interleukin 1 receptor antagonist
NOTCH3 notch 3
P2RX3 purinergic receptor P2X, ligand gated ion channel, 3
P2RX7 purinergic receptor P2X, ligand gated ion channel, 7
PANX1 pannexin 1
PMM2 phosphomannomutase 2
PNKD paroxysmal nonkinesigenic dyskinesia
PRRT2 proline-rich transmembrane protein 2
SCN1A sodium channel, voltage gated, type I alpha subunit
SLC2A1 solute carrier family 2 (facilitated glucose transporter), member 1
SLC4A4 solute carrier family 4 (sodium bicarbonate cotransporter), member 4
TGFBI transforming growth factor, beta-induced, 68kDa
TNF tumor necrosis factor