KCNA10
Potassium voltage-gated channel subfamily A member 10 also known as Kv1.8 is a protein that in humans is encoded by the KCNA10 gene.[1][1] The protein encoded by this gene is a voltage-gated potassium channel subunit.
References
- ↑ 1.0 1.1 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
- Landes GM, Curran ME, Keating MT (1995). "Molecular characterization and refined genomic localization of three human potassium ion channel genes.". Cytogenet. Cell Genet. 70 (3–4): 280–4. doi:10.1159/000134052. PMID 7789190.
- 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.
- Tian S, Liu W, Wu Y et al. (2002). "Regulation of the voltage-gated K+ channel KCNA10 by KCNA4B, a novel beta-subunit". Am. J. Physiol. Renal Physiol. 283 (1): F142–9. doi:10.1152/ajprenal.00258.2001. PMID 12060596.
- Orias M, Bray-Ward P, Curran ME et al. (1997). "Genomic localization of the human gene for KCNA10, a cGMP-activated K channel". Genomics 42 (1): 33–7. doi:10.1006/geno.1997.4712. PMID 9177773.
- Lang R, Lee G, Liu W et al. (2000). "KCNA10: a novel ion channel functionally related to both voltage-gated potassium and CNG cation channels". Am. J. Physiol. Renal Physiol. 278 (6): F1013–21. PMID 10836990.
- Yao X, Tian S, Chan HY et al. (2002). "Expression of KCNA10, a voltage-gated K channel, in glomerular endothelium and at the apical membrane of the renal proximal tubule". J. Am. Soc. Nephrol. 13 (12): 2831–9. doi:10.1097/01.ASN.0000036866.37886.C5. PMID 12444201.
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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