Biology:TRPM6

From HandWiki
Short description: Protein-coding gene in the species Homo sapiens


A representation of the 3D structure of the protein myoglobin showing turquoise α-helices.
Generic protein structure example


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

See also

References

  1. ↑ "Hypomagnesemia with secondary hypocalcemia is caused by mutations in TRPM6, a new member of the TRPM gene family". Nat. Genet. 31 (2): 166–70. 2002. 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. pp. 700. ISBN 978-94-007-0264-6. 
  • "Essential role for TRPM6 in epithelial magnesium transport and body magnesium homeostasis.". Pflügers Arch. 451 (1): 228–34. 2006. doi:10.1007/s00424-005-1470-y. PMID 16075242. 
  • "International Union of Pharmacology. XLIX. Nomenclature and structure-function relationships of transient receptor potential channels.". Pharmacol. Rev. 57 (4): 427–50. 2006. doi:10.1124/pr.57.4.6. PMID 16382100. 
  • Bödding M (2007). "TRPM6: A Janus-like protein". Transient Receptor Potential (TRP) Channels. Handbook of Experimental Pharmacology. 179. pp. 299–311. doi:10.1007/978-3-540-34891-7_18. ISBN 978-3-540-34889-4. 

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




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