Predicted PPI networks were based on the following genes, which are responsible for the majority of SPG cases: ATL1 (SPG3), SPAST (SPG4), CYP7B1 (SPG5A), RTN2 (SPG12), REEP1 (SPG31), and ZFYVE27 (SPG33). Here, ATL1 is linked to hereditary spastic paraplegia.