TRPC6

From Wikipedia, the free encyclopedia


Transient receptor potential cation channel, subfamily C, member 6
Identifiers
Symbol(s) TRPC6; FLJ11098; FLJ14863; FSGS2; TRP6
External IDs OMIM: 603652 MGI109523 HomoloGene37944
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)
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

  1. ^ 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:10.1126/science.1106215. 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:10.1093/ndt/gfh961. 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:10.1124/pr.57.4.6. 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:10.1016/j.semcdb.2006.11.003. PMID 17116414. 
  • Dietrich A, Gudermann T (2007). "TRPC6.". Handb Exp Pharmacol (179): 125–41. doi:10.1007/978-3-540-34891-7_7. PMID 17217054. 


[edit] External links