Phosphoenolpyruvate Carboxykinase Deficiency

Phosphoenolpyruvate Carboxykinase Deficiency, also known as phosphoenolpyruvate carboxykinase deficiency, is related to hypoglycemia and lactic acidosis, and has symptoms including cyanosis and seizures. An important gene associated with Phosphoenolpyruvate Carboxykinase Deficiency is PCK1 (Phosphoenolpyruvate Carboxykinase 1), and among its related pathways/superpathways are PI3K-Akt signaling pathway and Glycosaminoglycan metabolism. Affiliated tissues include liver, and related phenotype is Negative genetic interaction between PTTG1-/- and PTTG1+/+.