KCNV1
Potassium voltage-gated channel subfamily V member 1 is a protein that in humans is encoded by the KCNV1 gene.[1][2] The protein encoded by this gene is a voltage-gated potassium channel subunit.[1][2]
References
- ↑ 1.0 1.1 Hugnot JP, Salinas M, Lesage F, Guillemare E, de Weille J, Heurteaux C, Mattei MG, Lazdunski M (Aug 1996). "Kv8.1, a new neuronal potassium channel subunit with specific inhibitory properties towards Shab and Shaw channels". EMBO J 15 (13): 3322–31. PMC 451895. PMID 8670833.
- ↑ 2.0 2.1 Gutman GA, Chandy KG, Grissmer S, Lazdunski M, McKinnon D, Pardo LA, Robertson GA, Rudy B, Sanguinetti MC, Stuhmer W, Wang X (Dec 2005). "International Union of Pharmacology. LIII. Nomenclature and molecular relationships of voltage-gated potassium channels". Pharmacol Rev 57 (4): 473–508. doi:10.1124/pr.57.4.10. PMID 16382104.
Further reading
- Strausberg RL, Feingold EA, Grouse LH et al. (2002). "Generation and initial analysis of more than 15,000 full-length human and mouse cDNA sequences.". Proc. Natl. Acad. Sci. U.S.A. 99 (26): 16899–903. doi:10.1073/pnas.242603899. PMC 139241. PMID 12477932.
- Sano A, Mikami M, Nakamura M et al. (2002). "Positional candidate approach for the gene responsible for benign adult familial myoclonic epilepsy.". Epilepsia. 43 Suppl 9: 26–31. doi:10.1046/j.1528-1157.43.s.9.7.x. PMID 12383276.
- Ebihara M, Ohba H, Kikuchi M, Yoshikawa T (2004). "Structural characterization and promoter analysis of human potassium channel Kv8.1 (KCNV1) gene.". Gene 325: 89–96. doi:10.1016/j.gene.2003.09.044. PMID 14697513.
- Salinas M, de Weille J, Guillemare E et al. (1997). "Modes of regulation of shab K+ channel activity by the Kv8.1 subunit.". J. Biol. Chem. 272 (13): 8774–80. doi:10.1074/jbc.272.13.8774. PMID 9079713.
External links
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Index of cells |
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| Description |
- Structure
- Organelles
- peroxisome
- cytoskeleton
- centrosome
- epithelia
- cilia
- mitochondria
- Membranes
- Membrane transport
- ion channels
- vesicular transport
- solute carrier
- ABC transporters
- ATPase
- oxidoreduction-driven
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| Disease |
- Structural
- peroxisome
- cytoskeleton
- cilia
- mitochondria
- nucleus
- scleroprotein
- Membrane
- channelopathy
- solute carrier
- ATPase
- ABC transporters
- other
- extracellular ligands
- cell surface receptors
- intracellular signalling
- Vesicular transport
- Pore-forming toxins
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