hand muscle atrophy Gene Set
Genes
9 genes associated with the hand muscle atrophy phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
| Symbol |
Name |
|
ALS2
|
amyotrophic lateral sclerosis 2 (juvenile)
|
|
BSCL2
|
Berardinelli-Seip congenital lipodystrophy 2 (seipin)
|
|
DCTN1
|
dynactin 1
|
|
GARS
|
glycyl-tRNA synthetase
|
|
PLOD3
|
procollagen-lysine, 2-oxoglutarate 5-dioxygenase 3
|
|
SLC39A13
|
solute carrier family 39 (zinc transporter), member 13
|
|
SLC52A3
|
solute carrier family 52 (riboflavin transporter), member 3
|
|
SPG11
|
spastic paraplegia 11 (autosomal recessive)
|
|
TRPV4
|
transient receptor potential cation channel, subfamily V, member 4
|
