TRPM6

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Transient receptor potential cation channel, subfamily M, member 6
Identifiers
Symbol(s) TRPM6; CHAK2; HMGX; HOMG; HSH
External IDs OMIM: 607009 MGI2675603 HomoloGene9767
RNA expression pattern

More reference expression data

Orthologs
Human Mouse
Entrez 140803 225997
Ensembl ENSG00000119121 ENSMUSG00000024727
Uniprot Q9BX84 Q8CIR4
Refseq NM_017662 (mRNA)
NP_060132 (protein)
XM_987699 (mRNA)
XP_992793 (protein)
Location Chr 9: 76.53 - 76.69 Mb Chr 19: 18.82 - 18.96 Mb
Pubmed search [1] [2]

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


Contents

[edit] See also

[edit] References

  1. ^ 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. 

[edit] Further reading

  • Chubanov V, Gudermann T, Schlingmann KP (2006). "Essential role for TRPM6 in epithelial magnesium transport and body magnesium homeostasis.". Pflugers 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): 299–311. doi:10.1007/978-3-540-34891-7_18. PMID 17217065. 

[edit] External links

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