Tandem pore domain potassium channel

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Overview

Two-pore-domain potassium channels: This family of 15 members form what is known as "leak channels" which possess Goldman-Hodgkin-Katz (open) rectification.[1] These channels are regulated by several mechanisms including oxygen tension, pH, mechanical stretch, and G-proteins. Their name is derived from the fact that the α subunits consist of four transmembrane segments, each containing two pore loops. As such, they structurally correspond to two inward-rectifier α subunits and thus form dimers in the membrane.

Below is a list of the 15 known two-pore-domain human potassium channels:[1]

Gene Name
KCNK1 K2p01.1
KCNK2 K2p02.1
KCNK3 K2p03.1
KCNK4 K2p04.1
KCNK5 K2p05.1
KCNK6 K2p06.1
KCNK7 K2p07.1
KCNK9 K2p09.1
KCNK10 K2p10.1
KCNK12 K2p12.1
KCNK13 K2p13.1
KCNK15 K2p15.1
KCNK16 K2p16.1
KCNK17 K2p17.1
KCNK18 K2p18.1

See also

External links

References


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Acknowledgement and Attribution Regarding Sources of Content

Some of the initial content on this page may be incorporated in part from copyleft sources in the public domain including wikis such as Wikipedia and AskDrWiki. Drug information for patients came from the The National Library of Medicine. Infectious disease information may have come from the Centers for Disease Control (CDC). Differential Diagnoses are drawn from clinicians as well as an amalgamation of 3 sources: 1.The Disease Database; 2. Kahan, Scott, Smith, Ellen G. In A Page: Signs and Symptoms. Malden, Massachusetts: Blackwell Publishing, 2004:3; 3. Sailer, Christian, Wasner, Susanne. Differential Diagnosis Pocket. Hermosa Beach, CA: Borm Bruckmeir Publishing LLC, 2002:7 .

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