Citations for
1KCNB1, KCNG3, KCNG4
Mutation of histidine 105 in the T1 domain of the potassium channel Kv2.1 disrupts heteromerization with Kv6.3 and Kv6.4.
Mederos Y Schnitzler M, Rinné S, Skrobek L, Renigunta V, Schlichthörl G, Derst C, Gudermann T, Daut J, Preisig-Müller R.
J Biol Chem 284(7):4695-704. Epub 2008 Dec 11. 2009
2ADAD2, DNAAF1, DNAAF2, HSDL1, ICS14, KCNG4, MBPTS1, TAF1C
Deletions and point mutations of LRRC50 cause primary ciliary dyskinesia due to dynein arm defects.
Loges NT, Olbrich H, Becker-Heck A, Häffner K, Heer A, Reinhard C, Schmidts M, Kispert A, Zariwala MA, Leigh MW, Knowles MR, Zentgraf H, Seithe H, Nürnberg G, Nürnberg P, Reinhardt R, Omran H.
Am J Hum Genet 85(6):883-9. Epub .PMID: 19944400 2009
3KCNG3, KCNG4, KCNB1
Molecular cloning and characterization of Kv6.3, a novel modulatory subunit for voltage-gated K(+) channel Kv2.1.
Sano Y, Mochizuki S, Miyake A, Kitada C, Inamura K, Yokoi H, Nozawa K, Matsushime H, Furuichi K.
FEBS Lett 512(1-3):230-4. 2002
4KCNB1, KCNG3, KCNG4
Obligatory heterotetramerization of three previously uncharacterized Kv channel alpha-subunits identified in the human genome
Ottschytsch N, Raes A, Van Hoorick D, Snyders DJ.
Proc Natl Acad Sci U S A 99(12):7986-91. 2002