Paralogue Annotation for KCNQ1 residue 338

Residue details

Gene: KCNQ1
Reference Sequences: LRG: LRG_287, Ensembl variant: ENST00000155840 / ENSP00000155840
Amino Acid Position: 338
Reference Amino Acid: S - Serine
Protein Domain: Transmembrane/Linker/Pore


Paralogue Variants mapped to KCNQ1 residue 338

No paralogue variants have been mapped to residue 338 for KCNQ1.



KCNQ1VTVTTIGYGDKVPQTWVGKTIASCFSVFAI>S<FFALPAGILGSGFALKVQQKQRQKHFNRQI368
KCNQ2ITLTTIGYGDKYPQTWNGRLLAATFTLIGV>S<FFALPAGILGSGFALKVQEQHRQKHFEKRR333
KCNQ3ITLATIGYGDKTPKTWEGRLIAATFSLIGV>S<FFALPAGILGSGLALKVQEQHRQKHFEKRR372
KCNQ4ITLTTIGYGDKTPHTWLGRVLAAGFALLGI>S<FFALPAGILGSGFALKVQEQHRQKHFEKRR339
KCNQ5ITLTTIGYGDKTPLTWLGRLLSAGFALLGI>S<FFALPAGILGSGFALKVQEQHRQKHFEKRR367
KCNA1VSMTTVGYGDMYPVTIGGKIVGSLCAIAGV>L<TIALPVPVIVSNFNYFYHRETEGEEQAQLL428
KCNA10VTMTTVGYGDMCPTTPGGKIVGTLCAIAGV>L<TIALPVPVIVSNFNYFYHRETENEEKQNIP477
KCNA2VSMTTVGYGDMVPTTIGGKIVGSLCAIAGV>L<TIALPVPVIVSNFNYFYHRETEGEEQAQYL430
KCNA3VTMTTVGYGDMHPVTIGGKIVGSLCAIAGV>L<TIALPVPVIVSNFNYFYHRETEGEEQSQYM500
KCNA4VTMTTVGYGDMKPITVGGKIVGSLCAIAGV>L<TIALPVPVIVSNFNYFYHRETENEEQTQLT580
KCNA5VTMTTVGYGDMRPITVGGKIVGSLCAIAGV>L<TIALPVPVIVSNFNYFYHRETDHEEPAVLK536
KCNA6VTMTTVGYGDMYPMTVGGKIVGSLCAIAGV>L<TIALPVPVIVSNFNYFYHRETEQEEQGQYT478
KCNA7VTMTTVGYGDMAPVTVGGKIVGSLCAIAGV>L<TISLPVPVIVSNFSYFYHRETEGEEAGMFS414
KCNB1ITMTTVGYGDIYPKTLLGKIVGGLCCIAGV>L<VIALPIPIIVNNFSEFYKEQKRQEKAIKRR433
KCNB2ITMTTVGYGDIYPKTLLGKIVGGLCCIAGV>L<VIALPIPIIVNNFSEFYKEQKRQEKAIKRR437
KCNC1VTMTTLGYGDMYPQTWSGMLVGALCALAGV>L<TIAMPVPVIVNNFGMYYSLAMAKQKLPKKK456
KCNC2VTMTTLGYGDMYPQTWSGMLVGALCALAGV>L<TIAMPVPVIVNNFGMYYSLAMAKQKLPRKR493
KCNC3VTMTTLGYGDMYPKTWSGMLVGALCALAGV>L<TIAMPVPVIVNNFGMYYSLAMAKQKLPKKK559
KCNC4VTMTTLGYGDMYPKTWSGMLVGALCALAGV>L<TIAMPVPVIVNNFGMYYSLAMAKQKLPKKR492
KCND1VTMTTLGYGDMVPSTIAGKIFGSICSLSGV>L<VIALPVPVIVSNFSRIYHQNQRADKRRAQQ428
KCND2VTMTTLGYGDMVPKTIAGKIFGSICSLSGV>L<VIALPVPVIVSNFSRIYHQNQRADKRRAQK426
KCND3VTMTTLGYGDMVPKTIAGKIFGSICSLSGV>L<VIALPVPVIVSNFSRIYHQNQRADKRRAQK423
KCNF1ITMTTVGYGDIYPKTTLGKLNAAISFLCGV>I<AIALPIHPIINNFVRYYNKQRVLETAAKHE426
KCNG1ITMTTVGYGDMVPRSTPGQVVALSSILSGI>L<LMAFPVTSIFHTFSRSYLELKQEQERVMFR480
KCNG2ISMTTVGYGDMVPRSLPGQVVALSSILSGI>L<LMAFPVTSIFHTFSRSYSELKEQQQRAASP425
KCNG3ISMTTVGYGDMYPITVPGRILGGVCVVSGI>V<LLALPITFIYHSFVQCYHELKFRSARYSR-428
KCNG4ISMTTVGYGDMVPRSVPGQMVALSSILSGI>L<IMAFPATSIFHTFSHSYLELKKEQEQLQAR474
KCNS1VSMTTVGYGDVVPVTVAGKLAASGCILGGI>L<VVALPITIIFNKFSHFYRRQKALEAAVRNS477
KCNS2VSMTTVGYGDVVPGTTAGKLTASACILAGI>L<VVVLPITLIFNKFSHFYRRQKQLESAMRSC430
KCNS3ISMTTVGYGDTHPVTLAGKLIASTCIICGI>L<VVALPITIIFNKFSKYYQKQKDIDVDQCSE426
KCNV1TSMTTVGYGDIRPDTTTGKIVAFMCILSGI>L<VLALPIAIINDRFSACYFTLKLKEAAVRQR448
KCNV2VSISTVGYGDMYPETHLGRFFAFLCIAFGI>I<LNGMPISILYNKFSDYYSKLKAYEYTTIRR513
cons                              > <                              

See full Alignment of Paralogues


Known Variants in KCNQ1

ProteinCDSDisease ClassificationDiseasedbSNP linksEffect Prediction
p.S338Fc.1013C>T Inherited ArrhythmiaLQTSSIFT: deleterious
Polyphen: probably damaging
ReportsInherited ArrhythmiaLQTS The genetic basis of long QT and short QT syndromes: a mutation update. Hum Mutat. 2009 30(11):1486-511. 19862833
Inherited ArrhythmiaLQTS Dysfunctional potassium channel subunit interaction as a novel mechanism of long QT syndrome. Heart Rhythm. 2013 10(5):728-37. doi: 10.1016/j.hrthm.2012.12.033. 23291057
p.S338Cc.1013C>G Inherited ArrhythmiaLQTSSIFT:
Polyphen:
ReportsInherited ArrhythmiaLQTS Asymmetry of parental origin in long QT syndrome: preferential maternal transmission of KCNQ1 variants linked to channel dysfunction. Eur J Hum Genet. 2016 24(8):1160-6. doi: 10.1038/ejhg.2015.257. 26669661