CCNL1 and Autosomal recessive spastic paraplegia type 7: Each protein is represented as a node with edged interactions cdk10 cyclin dependent kinase 10;ZNF276 ZNF276 zin finger protein 276;FAM58A family with sequence similarity 58; ETS2 V-ets erythroblastosis virus E26 oncogene homolog 2 (avian); CCNL2 Cyclin L2; CCNL1 Cyclin L1; GALNS Galactosamine (Nacetyl)–sulfate sulfonate; SPG7 Spastic paraplegia 7 (pure and complicated autosomal recessive); CCNK, CyclinK; CCNH, CyclinH; CCNT1 CyclinT1; (Fig. 4a,b).