KCNH3
Potassium voltage-gated channel subfamily H member 3 is a protein that in humans is encoded by the KCNH3 gene.[1][2] The protein encoded by this gene is a voltage-gated potassium channel subunit.[1][2]
References
- ↑ 1.0 1.1 Miyake A, Mochizuki S, Yokoi H, Kohda M, Furuichi K (Sep 1999). "New ether-a-go-go K(+) channel family members localized in human telencephalon". J Biol Chem 274 (35): 25018–25. doi:10.1074/jbc.274.35.25018. PMID 10455180.
- ↑ 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
- Nagase T, Ishikawa K, Kikuno R et al. (1999). "Prediction of the coding sequences of unidentified human genes. XV. The complete sequences of 100 new cDNA clones from brain which code for large proteins in vitro.". DNA Res. 6 (5): 337–45. doi:10.1093/dnares/6.5.337. PMID 10574462.
- Zou A, Lin Z, Humble M et al. (2003). "Distribution and functional properties of human KCNH8 (Elk1) potassium channels.". Am. J. Physiol., Cell Physiol. 285 (6): C1356–66. doi:10.1152/ajpcell.00179.2003. PMID 12890647.
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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