Whether associated with these diseases or sporadic, angiomyolipomas are caused by mutations in either the TSC1 or TSC2 genes, which govern cell growth and proliferation.
TSC is a multisystem genetic disease with mutation in either TSC1 or TSC2 gene.
Protein kinase, AMP-activated, alpha 1 has been shown to interact with TSC2.
Tuberous sclerosis proteins 1 and 2, also known as TSC1 (hamartin) and TSC2 (tuberin), form a protein-complex.
TSC2 |