K2P6.1 potassium channel [Homo sapiens]

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Genetic modifiers of the severity of sickle cell anemia identified through a genome-wide association study. [Am J Hematol. 2010]
Genetic modifiers of the severity of sickle cell anemia identified through a genome-wide association study.
Sebastiani P, Solovieff N, Hartley SW, Milton JN, Riva A, Dworkis DA, Melista E, Klings ES, Garrett ME, Telen MJ, et al. Am J Hematol. 2010 Jan; 85(1):29-35.
Genomic structure, cochlear expression, and mutation screening of KCNK6, a candidate gene for DFNA4. [J Neurosci Res. 2004]
Genomic structure, cochlear expression, and mutation screening of KCNK6, a candidate gene for DFNA4.
Mhatre AN, Li J, Chen AF, Yost CS, Smith RJ, Kindler CH, Lalwani AK. J Neurosci Res. 2004 Jan 1; 75(1):25-31.
Assignment of KCNK6 encoding the human weak inward rectifier potassium channel TWIK-2 to chromosome band 19q13.1 by radiation hybrid mapping. [Cytogenet Cell Genet. 1999]
Assignment of KCNK6 encoding the human weak inward rectifier potassium channel TWIK-2 to chromosome band 19q13.1 by radiation hybrid mapping.
Gray AT, Kindler CH, Sampson ER, Yost CS. Cytogenet Cell Genet. 1999; 84(3-4):190-1.

RefSeq protein isoforms
See 3 reference sequence protein isoforms for the KCNK6 gene.

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Protein