Paroxysmal Kinesigenic Choreoathetosis Gene Set
Genes
13 genes associated with the disease Paroxysmal Kinesigenic Choreoathetosis in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
| Symbol |
Name |
|
CACNA1A
|
calcium channel, voltage-dependent, P/Q type, alpha 1A subunit
|
|
CHRNA4
|
cholinergic receptor, nicotinic, alpha 4 (neuronal)
|
|
COMT
|
catechol-O-methyltransferase
|
|
KCNA1
|
potassium channel, voltage gated shaker related subfamily A, member 1
|
|
KCNA5
|
potassium channel, voltage gated shaker related subfamily A, member 5
|
|
KCNA6
|
potassium channel, voltage gated shaker related subfamily A, member 6
|
|
NKX2-1
|
NK2 homeobox 1
|
|
PLEK
|
pleckstrin
|
|
PRKD1
|
protein kinase D1
|
|
PRRT2
|
proline-rich transmembrane protein 2
|
|
SGCE
|
sarcoglycan, epsilon
|
|
SLC2A1
|
solute carrier family 2 (facilitated glucose transporter), member 1
|
|
STX1B
|
syntaxin 1B
|
