Finally, for congenital myopathies, muscle development and calcium homeostasis seem to be the most significant processes, but muscle contraction-related terms also play a role, as well as processes not specific for skeletal muscle, such as catabolism of nucleotides - these appear enriched due to the association of DNM2 to the catabolism of GTP, as well as MYH7 and TPM2 to the catabolism of ATP. This evidence concerns the gene TPM2 and congenital myopathy.