Familial Dystonia Gene Set
Genes
15 genes associated with the disease Familial Dystonia in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
| Symbol |
Name |
|
ALDH5A1
|
aldehyde dehydrogenase 5 family, member A1
|
|
CACNA1A
|
calcium channel, voltage-dependent, P/Q type, alpha 1A subunit
|
|
DBH
|
dopamine beta-hydroxylase (dopamine beta-monooxygenase)
|
|
GCH1
|
GTP cyclohydrolase 1
|
|
GLRA1
|
glycine receptor, alpha 1
|
|
GNAL
|
guanine nucleotide binding protein (G protein), alpha activating activity polypeptide, olfactory type
|
|
KMT2B
|
lysine (K)-specific methyltransferase 2B
|
|
LRP2
|
low density lipoprotein receptor-related protein 2
|
|
MCF2L
|
MCF.2 cell line derived transforming sequence-like
|
|
PRKRA
|
protein kinase, interferon-inducible double stranded RNA dependent activator
|
|
PTS
|
6-pyruvoyltetrahydropterin synthase
|
|
SGCE
|
sarcoglycan, epsilon
|
|
THAP1
|
THAP domain containing, apoptosis associated protein 1
|
|
TOR1A
|
torsin family 1, member A (torsin A)
|
|
TUBB4A
|
tubulin, beta 4A class IVa
|
