Citations for
1INPP5J, KCNE1, KCNQ1
Phosphatidylinositol-4,5-bisphosphate is required for KCNQ1/KCNE1 channel function but not anterograde trafficking.
Royal AA, Tinker A, Harmer SC.
PLoS One 12(10):e0186293. doi: 10.1371/journal.pone.0186293. eCollection 2017. 2017
2AQP2, AQP3, KCNE1
Ménière's Disease: Molecular Analysis of Aquaporins 2, 3 and Potassium Channel KCNE1 Genes in Brazilian Patients.
Lopes Kde C, Sartorato EL, da Silva-Costa SM, de Macedo Adamov NS, Ganança FF.
Otol Neurotol 37(8):1117-21. doi: 10.1097/MAO.0000000000001136. 2016
3KCNE1, KCNQ1, SGMS1
Regulation of membrane KCNQ1/KCNE1 channel density by sphingomyelin synthase 1.
Wu M, Takemoto M, Taniguchi M, Takumi T, Okazaki T, Song WJ.
Am J Physiol Cell Physiol 311(1):C15-23. doi: 10.1152/ajpcell.00272.2015. Epub 2016 May 18. 2016
4BACE1, KCNE1, KCNQ1
BACE1 modulates gating of KCNQ1 (Kv7.1) and cardiac delayed rectifier KCNQ1/KCNE1 (IKs).
Agsten M, Hessler S, Lehnert S, Volk T, Rittger A, Hartmann S, Raab C, Kim DY, Groemer TW, Schwake M, Alzheimer C, Huth T.
J Mol Cell Cardiol 89(Pt B):335-48. doi: 10.1016/j.yjmcc.2015.10.006. Epub 2015 Oct 8. 2015
5KCNE1, KCNQ1, OXSR1, STK39
SPAK and OSR1 Sensitive Cell Membrane Protein Abundance and Activity of KCNQ1/E1 K+ Channels.
Elvira B, Warsi J, Fezai M, Munoz C, Lang F.
Cell Physiol Biochem 37(5):2032-42. doi: 10.1159/000438563. Epub 2015 Nov 20. 2015
6KCNE1, KCNE2, KCNQ1
Differential modulations of KCNQ1 by auxiliary proteins KCNE1 and KCNE2.
Li P, Liu H, Lai C, Sun P, Zeng W, Wu F, Zhang L, Wang S, Tian C, Ding J.
Sci Rep 4:4973. doi: 10.1038/srep04973. 2014
7KCNE1, KCNQ1, KL
Upregulation of KCNQ1/KCNE1 K+ channels by Klotho.
Almilaji A, Pakladok T, Muñoz C, Elvira B, Sopjani M, Lang F.
Channels (Austin) 8(3):222-9. 2014
8KCNE1
Structural investigation of the transmembrane domain of KCNE1 in proteoliposomes.
Sahu ID, Kroncke BM, Zhang R, Dunagan MM, Smith HJ, Craig A, McCarrick RM, Sanders CR, Lorigan GA.
Biochemistry 53(40):6392-401. doi: 10.1021/bi500943p. Epub 2014 Oct 3. 2014
9KCNE1, KCNE2
Differential modulations of KCNQ1 by auxiliary proteins KCNE1 and KCNE2.
Li P, Liu H, Lai C, Sun P, Zeng W, Wu F, Zhang L, Wang S, Tian C, Ding J.
Sci Rep 4:4973. doi: 10.1038/srep04973. 2014
10BACE1, KCNE1, KCNE2
BACE1 and presenilin/γ-secretase regulate proteolytic processing of KCNE1 and 2, auxiliary subunits of voltage-gated potassium channels.
Sachse CC, Kim YH, Agsten M, Huth T, Alzheimer C, Kovacs DM, Kim DY.
FASEB J 27(6):2458-67. doi: 10.1096/fj.12-214056. Epub 2013 Mar 15. 2013
11KCNE1, KCNQ1
Trafficking of the IKs -complex in MDCK cells: site of subunit assembly and determinants of polarized localization.
David JP, Andersen MN, Olesen SP, Rasmussen HB, Schmitt N.
Traffic 14(4):399-411. doi: 10.1111/tra.12042. Epub 2013 Feb 13. 2013
12KCNE1, KCNQ1
KCNQ1 channels do not undergo concerted but sequential gating transitions in both the absence and the presence of KCNE1 protein.
Meisel E, Dvir M, Haitin Y, Giladi M, Peretz A, Attali B.
J Biol Chem 287(41):34212-24. doi: 10.1074/jbc.M112.364901. Epub 2012 Aug 20. 2012
13KCNE1, KCNQ1
Regulation of KCNQ1/KCNE1 by β-catenin.
Wilmes J, Haddad-Tóvolli R, Alesutan I, Munoz C, Sopjani M, Pelzl L, Bogatikov E, Fedele G, Faggio C, Seebohm G, Föller M, Lang F.
Mol Membr Biol 29(3-4):87-94. doi: 10.3109/09687688.2012.678017. Epub 2012 May 14. 2012
14KCNE1
KCNE1 D85N polymorphism--a sex-specific modifier in type 1 long QT syndrome?
Lahtinen AM, Marjamaa A, Swan H, Kontula K.
BMC Med Genet 12:11. 2011
15KCNE1, KCNQ1
Analysis of the interactions between the C-terminal cytoplasmic domains of KCNQ1 and KCNE1 channel subunits.
Zheng R, Thompson K, Obeng-Gyimah E, Alessi D, Chen J, Cheng H, McDonald TV.
Biochem J 428(1):75-84.PMID: 20196769 2010
16KCNE1, KCNQ1
KCNE1 alters the voltage sensor movements necessary to open the KCNQ1 channel gate.
Osteen JD, Gonzalez C, Sampson KJ, Iyer V, Rebolledo S, Larsson HP, Kass RS.
Proc Natl Acad Sci U S A 107(52):22710-5. Epub 2010 Dec 13. 2010
17KCNE1, KCNQ1
Stoichiometry of the KCNQ1 - KCNE1 ion channel complex.
Nakajo K, Ulbrich MH, Kubo Y, Isacoff EY.
Proc Natl Acad Sci U S A 107(44):18862-7. Epub 2010 Oct 20. 2010
18KCNE1, KCNQ1
Identification of a protein-protein interaction between KCNE1 and the activation gate machinery of KCNQ1.
Lvov A, Gage SD, Berrios VM, Kobertz WR.
J Gen Physiol 135(6):607-18. Epub 2010 May 17. 2010
19KCNE1, SCN5A
Common variants in cardiac ion channel genes are associated with sudden cardiac death.
Albert CM, MacRae CA, Chasman DI, VanDenburgh M, Buring JE, Manson JE, Cook NR, Newton-Cheh C.
Circ Arrhythm Electrophysiol 3(3):222-9. Epub 2010 Apr 17. 2010
20KCNE1, LQT5
Mechanisms of disease pathogenesis in long QT syndrome type 5.
Harmer SC, Wilson AJ, Aldridge R, Tinker A.
Am J Physiol Cell Physiol 298(2):C263-73. Epub 2009 Nov 11. 2010
21KCNE1, KCNE2
Dynamic partnership between KCNQ1 and KCNE1 and influence on cardiac IKs current amplitude by KCNE2.
Jiang M, Xu X, Wang Y, Toyoda F, Liu XS, Zhang M, Robinson RB, Tseng GN.
J Biol Chem 284(24):16452-62. Epub 2009 Apr 16.PMID: 19372218 2009
22KCNE1, KCNQ1
Intracellular domains interactions and gated motions of I(KS) potassium channel subunits.
Haitin Y, Wiener R, Shaham D, Peretz A, Cohen EB, Shamgar L, Pongs O, Hirsch JA, Attali B.
EMBO J 28(14):1994-2005. Epub 2009 Jun 11. 2009
23KCNE1, KCNQ1
Functional interactions between KCNE1 C-terminus and the KCNQ1 channel.
Chen J, Zheng R, Melman YF, McDonald TV.
PLoS One 4(4):e5143. Epub 2009 Apr 2. 2009
24CLIC6, DEL21Q22, DSCR, FPDAML, KCNE1, RUNX1
Syndromic thrombocytopenia and predisposition to acute myelogenous leukemia caused by constitutional microdeletions on chromosome 21q.
Shinawi M, Erez A, Shardy DL, Lee B, Naeem R, Weissenberger G, Chinault AC, Cheung SW, Plon SE.
Blood 112(4):1042-7. Epub 2008 May 16. 2008
25KCNA1, KCNA5, KCNE1
Potassium channels involved in human sperm volume regulation--quantitative studies at the protein and mRNA levels.
Yeung CH, Cooper TG.
Mol Reprod Dev 75(4):659-68. 2008
26KCNE1, KCNQ1
Structure of KCNE1 and implications for how it modulates the KCNQ1 potassium channel.
Kang C, Tian C, Sönnichsen FD, Smith JA, Meiler J, George AL Jr, Vanoye CG, Kim HJ, Sanders CR.
Biochemistry 47(31):7999-8006. Epub 2008 Jul 9. 2008
27KCNE1, KCNE4, KCNQ1
KCNE4 can co-associate with the I(Ks) (KCNQ1-KCNE1) channel complex.
Manderfield LJ, George AL Jr.
FEBS J 275(6):1336-49. Epub 2008 Feb 14. 2008
28KCNE1
Preparation, functional characterization, and NMR studies of human KCNE1, a voltage-gated potassium channel accessory subunit associated with deafness and long QT syndrome.
Tian C, Vanoye CG, Kang C, Welch RC, Kim HJ, George AL Jr, Sanders CR.
Biochemistry 46(41):11459-72. Epub 2007 Sep 25. 2007
29KCNE1
Characterization of the cardiac KCNE1 gene promoter.
Mustapha Z, Pang L, Nattel S.
Cardiovasc Res 73(1):82-91. Epub 2006 Nov 10. 2007
30KCNE1, KCNQ1
Regulation of endocytic recycling of KCNQ1/KCNE1 potassium channels.
Seebohm G, Strutz-Seebohm N, Birkin R, Dell G, Bucci C, Spinosa MR, Baltaev R, Mack AF, Korniychuk G, Choudhury A, Marks D, Pagano RE, Attali B, Pfeufer A, Kass RS, Sanguinetti MC, Tavare JM, Lang F.
Circ Res 100(5):686-92. Epub 2007 Feb 9. 2007
31KCNE1
Upregulation of KCNE1 induces QT interval prolongation in patients with chronic heart failure.
Watanabe E, Yasui K, Kamiya K, Yamaguchi T, Sakuma I, Honjo H, Ozaki Y, Morimoto S, Hishida H, Kodama I.
Circ J 71(4):471-8. 2007
32KCNE1, KCNE2, KCNH2
Differential association between HERG and KCNE1 or KCNE2.
Um SY, McDonald TV.
PLoS One 2(9):e933.PMID: 17895974 2007
33KCNE1, LQT5
The role of abnormal trafficking of KCNE1 in long QT syndrome 5.
Harmer SC, Tinker A.
Biochem Soc Trans 35(Pt 5):1074-6. Review.PMID: 17956282 2007
34KCNQ1, LQT1, KCNE1, KCNE2, LQT5, LQT6, SCN5A, LQT3, KCNH2, LQT2
Spectrum of pathogenic mutations and associated polymorphisms in a cohort of 44 unrelated patients with long QT syndrome.
Millat G, Chevalier P, Restier-Miron L, Da Costa A, Bouvagnet P, Kugener B, Fayol L, Gonzalez Armengod C, Oddou B, Chanavat V, Froidefond E, Perraudin R, Rousson R, Rodriguez-Lafrasse C.
Clin Genet 70(3):214-27. 2006
35KCNE1, KCNE1L, KCNE2, KCNE3, KCNE4
Expression and transcriptional control of human KCNE genes.
Lundquist AL, Turner CL, Ballester LY, George AL Jr.
Genomics 87(1):119-28. Epub 2005 Nov 21. 2006
36KCNE1
Possible association of the human KCNE1 (minK) gene and QT interval in healthy subjects: evidence from association and linkage analyses in Israeli families.
Friedlander Y, Vatta M, Sotoodehnia N, Sinnreich R, Li H, Manor O, Towbin JA, Siscovick DS, Kark JD.
Ann Hum Genet 69(Pt 6):645-56. 2005
37KCNQ1, KCNE1, KCNH2, SCN5A
Association of KCNQ1, KCNE1, KCNH2 and SCN5A polymorphisms with QTc interval length in a healthy population.
Gouas L, Nicaud V, Berthet M, Forhan A, Tiret L, Balkau B, Guicheney P; D.
Eur J Hum Genet 13(11):1213-22. 2005
38KCNQ1, KCNH2, SCN5A, KCNE1, KCNE2
Single nucleotide polymorphism map of five long-QT genes.
Aydin A, Bahring S, Dahm S, Guenther UP, Uhlmann R, Busjahn A, Luft FC.
J Mol Med 83(2):159-65. Epub 2004 Dec 15. 2005
39KCNQ1, KCNE1
Impaired KCNQ1-KCNE1 and phosphatidylinositol-4,5-bisphosphate interaction underlies the long QT syndrome.
Park KH, Piron J, Dahimene S, Merot J, Baro I, Escande D, Loussouarn G.
Circ Res 96(7):730-9. Epub 2005 Mar 3. 2005
40KCNE1, KCNQ1, LQT1, LQT5
Dominant-negative I(Ks) suppression by KCNQ1-deltaF339 potassium channels linked to Romano-Ward syndrome.
Thomas D, Wimmer AB, Karle CA, Licka M, Alter M, Khalil M, Ulmer HE, Kathofer S, Kiehn J, Katus HA, Schoels W, Koenen M, Zehelein J.
Cardiovasc Res 67(3):487-97. 2005
41KCNE1, LQT5
Characterization of a novel Long QT syndrome mutation G52R-KCNE1 in a Chinese family.
Ma L, Lin C, Teng S, Chai Y, Bahring R, Vardanyan V, Li L, Pongs O, Hui R.
Cardiovasc Res 59(3):612-9. 2003
42AKAP9, KCNE1, KCNQ1
Requirement of a macromolecular signaling complex for beta adrenergic receptor modulation of the KCNQ1-KCNE1 potassium channel.
Marx SO, Kurokawa J, Reiken S, Motoike H, D'Armiento J, Marks AR, Kass RS.
Science 295(5554):496-9. 2002
43KCNE1, KCNQ1
KCNQ1/KCNE1 potassium channels in mammalian vestibular dark cells.
Nicolas M, Dememes D, Martin A, Kupershmidt S, Barhanin J.
Hear Res 153(1-2):132-45. 2001
44KCNE1, KCNQ1
Novel mutations in KvLQT1 that affect Iks activation through interactions with Isk.
Chouabe C, Neyroud N, Richard P, Denjoy I, Hainque B, Romey G, Drici MD, Guicheney P, Barhanin J.
Cardiovasc Res 45(4):971-80. 2000
45KCNE1, KCNH2, KCNQ1, SCN5A
Twenty single nucleotide polymorphisms (SNPs) and their allelic frequencies in four genes that are responsible for familial long QT syndrome in the Japanese population.
Iwasa H, Itoh T, Nagai R, Nakamura Y, Tanaka T.
J Hum Genet 45(3):182-3. 2000
46KCNE1, KCNE3, KCNK1
A constitutively open potassium channel formed by KCNQ1 and KCNE3.
Schroeder BC, Waldegger S, Fehr S, Bleich M, Warth R, Greger R, Jentsch TJ.
Nature 403(6766):196-9. 2000
47JLNS2, KCNE1, KCNF1, KCNQ1
Genomic structure of three long QT syndrome genes : KVLQT1, HERG, and KCNE1.
Splawski I, et al.
Genomics 51 : 86-97. 1998
48JLNS1, JLNS2, KCNQ1, KCNE1
IsK and KvLQT1: mutation in either of the two subunits of the slow component of the delayed rectifier potassium channel can cause Jervell and Lange-Nielsen syndrome.
Tyson J, Tranebjaerg L, Bellman S, Wren C, Taylor JF, Bathen J, Aslaksen B, Sorland SJ, Lund O, Malcolm S, Pembrey M, Bhattacharya S, Bitner-Glindzicz M.
Hum Mol Genet 6(12):2179-85. 1997
49JLNS2, KCNE1
KCNE1 mutations cause Jervell and Lange-Nielsen syndrome.
Schulze-Bahr E, Wang Q, Wedekind H, Haverkamp W, Chen Q, Sun Y, Rubie C, Hordt M, Towbin JA, Borggrefe M, Assmann G, Qu X, Somberg JC, Breithardt G, Oberti C, Funke H.
Nat Genet 17(3):267-8. No abstract available. 1997
50KCNE1, KCNE2
A minK-HERG complex regulates the cardiac potassium current I(Kr).
McDonald TV, et al.
Nature 388(6639):289-92. 1997
51KCNE1, KCNQ1
K(V)LQT1 and IsK (minK) proteins associate to form the I(Ks) cardiac potassium current.
Barhanin J, et al.
Nature 384 : 78-80. 1996
52KCNE1, KCNQ1
Coassembly of K(V)LQT1 and minK (IsK) proteins to form cardiac I(Ks) potassium channel.
Sanguinetti MC, et al.
Nature 384 : 80-83. 1996
53KCNE1
Gene assignment by polymerase chain reaction : localization of the human potassium channel I sK gene to the Down's syndrome region of chromosome 21q22.1-q22.2.
Malo MS, et al.
Gene 159 : 273-275. 1995
54KCNE1
Polymorphism of the gene encoding a human minimal potassium ion channel (minK).
Lai LP, et al.
Gene 151 : 339-340. 1994
55KCNE1
Localization of a potassium channel gene (KCNE1) to 21q22.1-q22.2 by in situ hybridization and somatic cell hybridization.
Chevillard C, et al.
Genomics 15 : 243-245. 1993
56KCNA1, KCNA2, KCNA5, KCNA7, KCNC2, KCNC3, KCNC4, KCNE1
Chromosomal localization of 7 potassium channel genes.
McPherson JD, et al.
(HGM11) Cytogenet Cell Genet 58 : 1979. 1991
57KCNE1
Molecular cloning and sequence analysis of human genomic DNA encoding a novel membrane protein which exhibits a slowly activating potassium channel activity.
Murai T, et al.
Biochem Biophys Res Commun 161(1):176-81. 1989