Dyskinesias, Paroxysmal Gene Set
Genes
14 genes associated with the disease Dyskinesias, Paroxysmal in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
| Symbol |
Name |
|
CACNA2D2
|
calcium channel, voltage-dependent, alpha 2/delta subunit 2
|
|
ECHS1
|
enoyl CoA hydratase, short chain, 1, mitochondrial
|
|
FGF14
|
fibroblast growth factor 14
|
|
KCNMA1
|
potassium channel, calcium activated large conductance subfamily M alpha, member 1
|
|
KMT2B
|
lysine (K)-specific methyltransferase 2B
|
|
NKX2-1
|
NK2 homeobox 1
|
|
PIGN
|
phosphatidylinositol glycan anchor biosynthesis, class N
|
|
PNKD
|
paroxysmal nonkinesigenic dyskinesia
|
|
PRRT2
|
proline-rich transmembrane protein 2
|
|
SCN2A
|
sodium channel, voltage gated, type II alpha subunit
|
|
SCN8A
|
sodium channel, voltage gated, type VIII alpha subunit
|
|
SLC16A2
|
solute carrier family 16, member 2 (thyroid hormone transporter)
|
|
SLC2A1
|
solute carrier family 2 (facilitated glucose transporter), member 1
|
|
TAF1
|
TAF1 RNA polymerase II, TATA box binding protein (TBP)-associated factor, 250kDa
|
