TRPM6
| Transient receptor potential cation channel, subfamily M, member 6 | |||||||||||
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| Identifiers | |||||||||||
| Symbols | TRPM6 ; CHAK2; HMGX; HOMG; HSH | ||||||||||
| External IDs | Template:OMIM5 Template:MGI HomoloGene: 9767 | ||||||||||
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| RNA expression pattern | |||||||||||
| File:PBB GE TRPM6 221102 s at tn.png | |||||||||||
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| Template:GNF Ortholog box | |||||||||||
| Species | Human | Mouse | |||||||||
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| RefSeq (protein) | n/a | n/a | |||||||||
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TRPM6 is a transient receptor potential ion channel associated with hypomagnesemia with secondary hypocalcemia.[1]
See also
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
- 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.
External links
- TRPM6+protein,+human at the US National Library of Medicine Medical Subject Headings (MeSH)
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This article incorporates text from the United States National Library of Medicine, which is in the public domain.