For example, WDR82 facilitates the establishment of mouse iPS cells by modulating mitochondrial oxidative phosphorylation and glycolysis.[32] Similarly, WD repeat‐containing protein 7 (FBW7) enhances aerobic glycolysis in pancreatic cancer cells by regulating the expression of cMYC.[33] Our findings demonstrated that WDR36 absence disturbs glucose metabolism during the late formation stage of blastoids. The gene discussed is FBXW7; the disease is pancreatic neoplasm.