A pathway analysis performed with GeneTrail2 [33] including all known and potential MEOX2 binding partners (obtained from the Integrated Interaction Database [35]) revealed that MEOX2 interacting partners are involved in a number of pathways previously related to DMD pathophysiology such as NF-κB and SMAD signalling. The gene discussed is NFKB1; the disease is Duchenne muscular dystrophy.