1 | KCNB1, 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
|
2 | ADAD2, 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
|
3 | KCNG3, 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
|
4 | KCNB1, 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
|