TRPM6

TRPM6 is a transient receptor potential ion channel associated with hypomagnesemia with secondary hypocalcemia.^[1]

References

↑ Schlingmann KP, Weber S, Peters M, et al. (2002). “Hypomagnesemia with secondary hypocalcemia is caused by mutations in TRPM6, a new member of the TRPM gene family”. Nat. Genet. 31 (2): 166–70. doi:10.1038/ng889. PMID 12032568.

Further reading

Islam, Md. Shahidul (January 2011). Transient Receptor Potential Channels. Advances in Experimental Medicine and Biology. 704. Berlin: Springer. p. 700. ISBN 978-94-007-0264-6.
Chubanov V, Gudermann T, Schlingmann KP (2006). “Essential role for TRPM6 in epithelial magnesium transport and body magnesium homeostasis”. Pflügers Arch. 451 (1): 228–34. doi:10.1007/s00424-005-1470-y. PMID 16075242.
Clapham DE, Julius D, Montell C, Schultz G (2006). “International Union of Pharmacology. XLIX. Nomenclature and structure-function relationships of transient receptor potential channels”. Pharmacol. Rev. 57 (4): 427–50. doi:10.1124/pr.57.4.6. PMID 16382100.
Bödding M (2007). “TRPM6: A Janus-like protein”. Handb Exp Pharmacol. 179 (179): 299–311. doi:10.1007/978-3-540-34891-7_18. PMID 17217065.

External links

TRPM6+protein,+human at the US National Library of Medicine Medical Subject Headings (MeSH)

This article incorporates text from the United States National Library of Medicine, which is in the public domain.