Ramsay Hunt Paralysis Syndrome Gene Set
Genes
28 genes associated with the disease Ramsay Hunt Paralysis Syndrome in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
| Symbol |
Name |
|
ALDH1A1
|
aldehyde dehydrogenase 1 family, member A1
|
|
ALDH1A2
|
aldehyde dehydrogenase 1 family, member A2
|
|
ATP13A2
|
ATPase type 13A2
|
|
ATP1A3
|
ATPase, Na+/K+ transporting, alpha 3 polypeptide
|
|
DCTN1
|
dynactin 1
|
|
DDC
|
dopa decarboxylase (aromatic L-amino acid decarboxylase)
|
|
DRD2
|
dopamine receptor D2
|
|
GBA
|
glucosidase, beta, acid
|
|
GDNF
|
glial cell derived neurotrophic factor
|
|
GSR
|
glutathione reductase
|
|
HTRA2
|
HtrA serine peptidase 2
|
|
LRRK2
|
leucine-rich repeat kinase 2
|
|
MAPT
|
microtubule-associated protein tau
|
|
NGF
|
nerve growth factor (beta polypeptide)
|
|
PARK2
|
parkin RBR E3 ubiquitin protein ligase
|
|
PARK7
|
parkinson protein 7
|
|
PARP1
|
poly (ADP-ribose) polymerase 1
|
|
PDYN
|
prodynorphin
|
|
PINK1
|
PTEN induced putative kinase 1
|
|
PNOC
|
prepronociceptin
|
|
POLG
|
polymerase (DNA directed), gamma
|
|
PRKCD
|
protein kinase C, delta
|
|
PRKRA
|
protein kinase, interferon-inducible double stranded RNA dependent activator
|
|
PRL
|
prolactin
|
|
SLC18A2
|
solute carrier family 18 (vesicular monoamine transporter), member 2
|
|
SLC30A10
|
solute carrier family 30, member 10
|
|
SNCA
|
synuclein, alpha (non A4 component of amyloid precursor)
|
|
TH
|
tyrosine hydroxylase
|
