congenital structural myopathy Gene Set

Dataset DISEASES Curated Gene-Disease Assocation Evidence Scores
Category disease or phenotype associations
Type disease
Similar Terms
Downloads & Tools

Genes

9 genes involed in the disease congenital structural myopathy from the DISEASES Curated Gene-Disease Assocation Evidence Scores dataset.

Symbol Name
ACTA1 actin, alpha 1, skeletal muscle
CFL2 cofilin 2 (muscle)
KBTBD13 kelch repeat and BTB (POZ) domain containing 13
KLHL40 kelch-like family member 40
NEB nebulin
RYR1 ryanodine receptor 1 (skeletal)
TNNT1 troponin T type 1 (skeletal, slow)
TPM2 tropomyosin 2 (beta)
TPM3 tropomyosin 3