Paralogue Annotation for KCNQ1 residue 353

Residue details

Gene: KCNQ1
Reference Sequences: LRG: LRG_287, Ensembl variant: ENST00000155840 / ENSP00000155840
Amino Acid Position: 353
Reference Amino Acid: L - Leucine
Protein Domain: C-terminus


Paralogue Variants mapped to KCNQ1 residue 353

No paralogue variants have been mapped to residue 353 for KCNQ1.



KCNQ1WVGKTIASCFSVFAISFFALPAGILGSGFA>L<KVQQKQRQKHFNRQIPA--AASLI-QTAWR380
KCNQ2WNGRLLAATFTLIGVSFFALPAGILGSGFA>L<KVQEQHRQKHFEKRRNP--AAGLI-QSAWR345
KCNQ3WEGRLIAATFSLIGVSFFALPAGILGSGLA>L<KVQEQHRQKHFEKRRKP--AAELI-QAAWR384
KCNQ4WLGRVLAAGFALLGISFFALPAGILGSGFA>L<KVQEQHRQKHFEKRRMP--AANLI-QAAWR351
KCNQ5WLGRLLSAGFALLGISFFALPAGILGSGFA>L<KVQEQHRQKHFEKRRNP--AANLI-QCVWR379
KCNA1IGGKIVGSLCAIAGVLTIALPVPVIVSNFN>Y<FYHRETEGEEQAQLLH-----VS--SP-NL435
KCNA10PGGKIVGTLCAIAGVLTIALPVPVIVSNFN>Y<FYHRETENEEKQNIPGEIERI---------483
KCNA2IGGKIVGSLCAIAGVLTIALPVPVIVSNFN>Y<FYHRETEGEEQAQYLQ-----VT--SCPKI438
KCNA3IGGKIVGSLCAIAGVLTIALPVPVIVSNFN>Y<FYHRETEGEEQSQYMH-----VG--SCQHL508
KCNA4VGGKIVGSLCAIAGVLTIALPVPVIVSNFN>Y<FYHRETENEEQTQLTQ-----NAV-SCPYL589
KCNA5VGGKIVGSLCAIAGVLTIALPVPVIVSNFN>Y<FYHRETDHEEPAVLKEE--QGTQS-QGPGL548
KCNA6VGGKIVGSLCAIAGVLTIALPVPVIVSNFN>Y<FYHRETEQEEQGQYTHV-------------480
KCNA7VGGKIVGSLCAIAGVLTISLPVPVIVSNFS>Y<FYHRETEGEEAGMFSHV-------------416
KCNB1LLGKIVGGLCCIAGVLVIALPIPIIVNNFS>E<FYKEQKRQEKAIKRREA--LERA--KRNG-443
KCNB2LLGKIVGGLCCIAGVLVIALPIPIIVNNFS>E<FYKEQKRQEKAIKRREA--LERA--KRNG-447
KCNC1WSGMLVGALCALAGVLTIAMPVPVIVNNFG>M<YYSLAMAKQKLPKKKKK--HIPR--PPQLG467
KCNC2WSGMLVGALCALAGVLTIAMPVPVIVNNFG>M<YYSLAMAKQKLPRKRKK--HIPP--APQAS504
KCNC3WSGMLVGALCALAGVLTIAMPVPVIVNNFG>M<YYSLAMAKQKLPKKKNK--HIPR--PPQPG570
KCNC4WSGMLVGALCALAGVLTIAMPVPVIVNNFG>M<YYSLAMAKQKLPKKRKK--HVPR--PAQLE503
KCND1IAGKIFGSICSLSGVLVIALPVPVIVSNFS>R<IYHQNQRADKRRAQQKV--RLARIRLAKSG441
KCND2IAGKIFGSICSLSGVLVIALPVPVIVSNFS>R<IYHQNQRADKRRAQKKA--RLARIRAAKSG439
KCND3IAGKIFGSICSLSGVLVIALPVPVIVSNFS>R<IYHQNQRADKRRAQKKA--RLARIRVAKTG436
KCNF1TLGKLNAAISFLCGVIAIALPIHPIINNFV>R<YYNKQRVLETAAKHELE--LMEL--N----433
KCNG1TPGQVVALSSILSGILLMAFPVTSIFHTFS>R<SYLELKQEQERVMFRRA--QFLI----K-T488
KCNG2LPGQVVALSSILSGILLMAFPVTSIFHTFS>R<SYSELKEQQQRAASPEP--ALQE----D-S433
KCNG3VPGRILGGVCVVSGIVLLALPITFIYHSFV>Q<CYHELKFRSARYSR----------------428
KCNG4VPGQMVALSSILSGILIMAFPATSIFHTFS>H<SYLELKKEQEQLQARLR--HLQN----T-G482
KCNS1VAGKLAASGCILGGILVVALPITIIFNKFS>H<FYRRQKALEAAVRNSNH--QEFE--D----484
KCNS2TAGKLTASACILAGILVVVLPITLIFNKFS>H<FYRRQKQLESAMRSCDF--GDGM--K----437
KCNS3LAGKLIASTCIICGILVVALPITIIFNKFS>K<YYQKQKDIDVDQCSEDA--PEKC--H----433
KCNV1TTGKIVAFMCILSGILVLALPIAIINDRFS>A<CYFTLKLKEAAVRQREA--LKKL--TKNIA459
KCNV2HLGRFFAFLCIAFGIILNGMPISILYNKFS>D<YYSKLKAYEYTTIRRER--GEVN--F----520
cons                              > <                              

See full Alignment of Paralogues


Known Variants in KCNQ1

ProteinCDSDisease ClassificationDiseasedbSNP linksEffect Prediction
p.L353Pc.1058T>C Inherited ArrhythmiaLQTSSIFT: deleterious
Polyphen: probably damaging
ReportsInherited ArrhythmiaLQTS Genomic structure of three long QT syndrome genes: KVLQT1, HERG, and KCNE1. Genomics. 1998 51(1):86-97. 9693036
Inherited ArrhythmiaLQTS Compendium of cardiac channel mutations in 541 consecutive unrelated patients referred for long QT syndrome genetic testing. Heart Rhythm. 2005 2(5):507-17. 15840476
Inherited ArrhythmiaLQTS Genetic testing for long-QT syndrome: distinguishing pathogenic mutations from benign variants. Circulation. 2009 120(18):1752-60. 19841300
Inherited ArrhythmiaLQTS Clinical aspects of type-1 long-QT syndrome by location, coding type, and biophysical function of mutations involving the KCNQ1 gene. Circulation. 2007 115(19):2481-9. 17470695
Inherited ArrhythmiaLQTS Phylogenetic and physicochemical analyses enhance the classification of rare nonsynonymous single nucleotide variants in type 1 and 2 long-QT syndrome. Circ Cardiovasc Genet. 2012 5(5):519-28. doi: 10.1161/CIRCGENETICS.112.963785. 22949429