Hypokalemia

About the Disease
Hypokalemia, also known as potassium deficiency, is related to gitelman syndrome and hypokalemic periodic paralysis, type 1. An important gene associated with Hypokalemia is SLC12A3 (Solute Carrier Family 12 Member 3), and among its related pathways/superpathways are Glucose / Energy Metabolism and Metabolism of steroids. The drugs Prednisolone phosphate and Prednisolone acetate have been mentioned in the context of this disorder. Affiliated tissues include kidney, heart and smooth muscle, and related phenotypes are homeostasis/metabolism and renal/urinary system

Common Targets
NR3C2 | SLC12A2 | MIR6863 | SLC12A3 | KCND3 | KCNJ16 | SCNN1B | FCGR3A | SCN4A | KCNA5 | CLDN10 | WNK1 | RET | SLC12A1 | OPRK1

Note: If you'd like to get a target analysis report for Hypokalemia, or if you are interested to learn how our AI-powered BDE-Chem can design therapeutic molecules to interact with the target(s) above against the disease of Hypokalemia at a cost 90% lower than traditional approaches, please feel free to contact us at BD@silexon.tech.

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