Neuromuscular Dysphagia Gene Set
Genes
12 genes associated with the disease Neuromuscular Dysphagia in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
| Symbol |
Name |
|
ACTA1
|
actin, alpha 1, skeletal muscle
|
|
COQ2
|
coenzyme Q2 4-hydroxybenzoate polyprenyltransferase
|
|
FARS2
|
phenylalanyl-tRNA synthetase 2, mitochondrial
|
|
KBTBD13
|
kelch repeat and BTB (POZ) domain containing 13
|
|
KLHL41
|
kelch-like family member 41
|
|
MAPT
|
microtubule-associated protein tau
|
|
MYPN
|
myopalladin
|
|
NEB
|
nebulin
|
|
SLC25A42
|
solute carrier family 25, member 42
|
|
TPM2
|
tropomyosin 2 (beta)
|
|
TPM3
|
tropomyosin 3
|
|
TWNK
|
twinkle mtDNA helicase
|
