abnormality of the musculature of the hand Gene Set
Genes
20 genes associated with the abnormality of the musculature of the hand 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
|
|
FBXO38
|
F-box protein 38
|
|
FGF10
|
fibroblast growth factor 10
|
|
FGFR2
|
fibroblast growth factor receptor 2
|
|
FGFR3
|
fibroblast growth factor receptor 3
|
|
GARS
|
glycyl-tRNA synthetase
|
|
HOXA13
|
homeobox A13
|
|
KANSL1
|
KAT8 regulatory NSL complex subunit 1
|
|
MYH7
|
myosin, heavy chain 7, cardiac muscle, beta
|
|
NEFL
|
neurofilament, light polypeptide
|
|
PLOD3
|
procollagen-lysine, 2-oxoglutarate 5-dioxygenase 3
|
|
RPL11
|
ribosomal protein L11
|
|
SALL4
|
spalt-like transcription factor 4
|
|
SLC39A13
|
solute carrier family 39 (zinc transporter), member 13
|
|
SLC52A3
|
solute carrier family 52 (riboflavin transporter), member 3
|
|
SPG11
|
spastic paraplegia 11 (autosomal recessive)
|
|
STIM1
|
stromal interaction molecule 1
|
|
TRPV4
|
transient receptor potential cation channel, subfamily V, member 4
|
