TRPC6
From Wikipedia, the free encyclopedia
Transient receptor potential cation channel, subfamily C, member 6
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Identifiers | ||||||||||||||
Symbol(s) | TRPC6; FLJ11098; FLJ14863; FSGS2; TRP6 | |||||||||||||
External IDs | OMIM: 603652 MGI: 109523 HomoloGene: 37944 | |||||||||||||
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Orthologs | ||||||||||||||
Human | Mouse | |||||||||||||
Entrez | 7225 | 22068 | ||||||||||||
Ensembl | n/a | ENSMUSG00000031997 | ||||||||||||
Uniprot | n/a | Q61143 | ||||||||||||
Refseq | NM_004621 (mRNA) NP_004612 (protein) |
NM_013838 (mRNA) NP_038866 (protein) |
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Location | n/a | Chr 9: 8.54 - 8.64 Mb | ||||||||||||
Pubmed search | [1] | [2] |
Transient receptor potential cation channel, subfamily C, member 6, also known as TRPC6, is a human gene.
TRPC6 is a transient receptor potential ion channel associated with focal segmental glomerulosclerosis.[1]
[edit] References
- ^ Winn MP, Conlon PJ, Lynn KL, et al (2005). "A mutation in the TRPC6 cation channel causes familial focal segmental glomerulosclerosis". Science 308 (5729): 1801–4. doi: . PMID 15879175.
[edit] Further reading
- Heiner I, Eisfeld J, Lückhoff A (2004). "Role and regulation of TRP channels in neutrophil granulocytes.". Cell Calcium 33 (5-6): 533–40. PMID 12765698.
- Walz G (2006). "Slit or pore? A mutation of the ion channel TRPC6 causes FSGS.". Nephrol. Dial. Transplant. 20 (9): 1777–9. doi: . PMID 15998650.
- 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: . PMID 16382100.
- Schlöndorff JS, Pollak MR (2007). "TRPC6 in glomerular health and disease: what we know and what we believe.". Semin. Cell Dev. Biol. 17 (6): 667–74. doi: . PMID 17116414.
- Dietrich A, Gudermann T (2007). "TRPC6.". Handb Exp Pharmacol (179): 125–41. doi: . PMID 17217054.
[edit] External links
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