Neuromuscular Diseases Gene Set

Dataset HuGE Navigator Gene-Phenotype Associations
Category disease or phenotype associations
Type phenotype
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Genes

13 genes associated with the Neuromuscular Diseases phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset.

Symbol Name
AMPD1 adenosine monophosphate deaminase 1
ATXN3 ataxin 3
DES desmin
DMD dystrophin
DMPK dystrophia myotonica-protein kinase
LMNA lamin A/C
MYH7 myosin, heavy chain 7, cardiac muscle, beta
SCN5A sodium channel, voltage gated, type V alpha subunit
SGCB sarcoglycan, beta (43kDa dystrophin-associated glycoprotein)
TNNI3 troponin I type 3 (cardiac)
TNNT2 troponin T type 2 (cardiac)
TPM1 tropomyosin 1 (alpha)
TRL-TAG1-1 transfer RNA-Leu (TAG) 1-1