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CNNM3 encodes a membrane protein with four transmembrane domains, two CBS (Cystathionine beta-synthase) domains, a DUF21 domain, and a cyclic nucleotide monophosphate (cNMP)-binding domain. It most likely functions as a transporter of divalent metal cations, especially magnesium, across cellular membranes, playing a critical role in magnesium ion homeostasis. It interacts with the TRPM7 channel to stimulate divalent cation entry into cells. Diseases associated with CNNM3 include Jalili Syndrome and Fanconi Anemia. This protein is conserved across vertebrates, highlighting its importance in physiology.
Drugs that modulate divalent cation (particularly magnesium) transport or affect channel interactions (such as blocking TRPM7 interaction, or altering magnesium homeostasis)
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