Mitochondrial Myopathies Gene Set

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

9 genes associated with the Mitochondrial Myopathies phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset.

Symbol Name
GLA galactosidase, alpha
HADHA hydroxyacyl-CoA dehydrogenase/3-ketoacyl-CoA thiolase/enoyl-CoA hydratase (trifunctional protein), alpha subunit
MT-TK tRNA
MT-TL1 tRNA
MYBPC3 myosin binding protein C, cardiac
MYH7 myosin, heavy chain 7, cardiac muscle, beta
MYL3 myosin, light chain 3, alkali; ventricular, skeletal, slow
TNNI3 troponin I type 3 (cardiac)
TNNT2 troponin T type 2 (cardiac)