Paralogue Annotation for KCNQ1 residue 282

Residue details

Gene: KCNQ1
Reference Sequences: LRG: LRG_287, Ensembl variant: ENST00000155840 / ENSP00000155840
Amino Acid Position: 282
Reference Amino Acid: L - Leucine
Protein Domain: Transmembrane/Linker/Pore


Paralogue Variants mapped to KCNQ1 residue 282

No paralogue variants have been mapped to residue 282 for KCNQ1.



KCNQ1GSVVFIHRQELITTLYIGFLGLIFSSYFVY>L<AEKDAVN-----ESGRVEFGSYADALWWGV307
KCNQ2GSVVYAHSKELVTAWYIGFLCLILASFLVY>L<AEKGE----------NDHFDTYADALWWGL272
KCNQ3GSAICAHSKELITAWYIGFLTLILSSFLVY>L<VEKDVPEVDAQGEEMKEEFETYADALWWGL311
KCNQ4GSVVYAHSKELITAWYIGFLVLIFASFLVY>L<AEKDA----------NSDFSSYADSLWWGT278
KCNQ5GSVVYAHSKELITAWYIGFLVLIFSSFLVY>L<VEKDA----------NKEFSTYADALWWGT306
KCNA1GQTLKASMRELGLLIFFLFIGVILFSSAVY>F<AEAEE---------AESHFSSIPDAFWWAV367
KCNA10GQTLKASMRELGLLIFFLFIGVILFSSAVY>F<AEVDE---------PESHFSSIPDGFWWAV416
KCNA2GQTLKASMRELGLLIFFLFIGVILFSSAVY>F<AEADE---------RESQFPSIPDAFWWAV369
KCNA3GQTLKASMRELGLLIFFLFIGVILFSSAVY>F<AEADD---------PTSGFSSIPDAFWWAV439
KCNA4GHTLRASMRELGLLIFFLFIGVILFSSAVY>F<AEADE---------PTTHFQSIPDAFWWAV519
KCNA5GKTLQASMRELGLLIFFLFIGVILFSSAVY>F<AEADN---------QGTHFSSIPDAFWWAV475
KCNA6GKTLQASMRELGLLIFFLFIGVILFSSAVY>F<AEADD---------DDSLFPSIPDAFWWAV417
KCNA7GQTLRASMRELGLLIFFLFIGVVLFSSAVY>F<AEVDR---------VDSHFTSIPESFWWAV353
KCNB1GFTLRRSYNELGLLILFLAMGIMIFSSLVF>F<AEKDE---------DDTKFKSIPASFWWAT372
KCNB2GFTLRRSYNELGLLILFLAMGIMIFSSLVF>F<AEKDE---------DATKFTSIPASFWWAT376
KCNC1GHTLRASTNEFLLLIIFLALGVLIFATMIY>Y<AERIGAQPNDPSASEHTHFKNIPIGFWWAV395
KCNC2GHTLRASTNEFLLLIIFLALGVLIFATMIY>Y<AERVGAQPNDPSASEHTQFKNIPIGFWWAV432
KCNC3GHTLRASTNEFLLLIIFLALGVLIFATMIY>Y<AERIGADPDDILGSNHTYFKNIPIGFWWAV498
KCNC4GHTLRASTNEFLLLIIFLALGVLIFATMIY>Y<AERIGARPSDPRGNDHTDFKNIPIGFWWAV431
KCND1GYTLKSCASELGFLLFSLTMAIIIFATVMF>Y<AEKGT---------NKTNFTSIPAAFWYTI367
KCND2GYTLKSCASELGFLLFSLTMAIIIFATVMF>Y<AEKGS---------SASKFTSIPAAFWYTI365
KCND3GYTLKSCASELGFLLFSLTMAIIIFATVMF>Y<AEKGS---------SASKFTSIPASFWYTI362
KCNF1TYALKRSFKELGLLLMYLAVGIFVFSALGY>T<MEQSH---------PETLFKSIPQSFWWAI365
KCNG1GLTARRCTREFGLLLLFLCVAIALFAPLLY>V<IENEM-----A---DSPEFTSIPACYWWAV419
KCNG2GLTMRRCAREFGLLLLFLCVAMALFAPLVH>L<AEREL-----G---ARRDFSSVPASYWWAV364
KCNG3GLTLKRCYREMVMLLVFICVAMAIFSALSQ>L<LEHGL-----DLETSNKDFTSIPAACWWVI368
KCNG4GLTVRRCTREFGLLLLFLAVAITLFSPLVY>V<AEKES-----G---RVLEFTSIPASYWWAI413
KCNS1GATLKHSYREVGILLLYLAVGVSVFSGVAY>T<AEKEE----------DVGFNTIPACWWWGT416
KCNS2GATLKYSYKEVGLLLLYLSVGISIFSVVAY>T<IEKEE----------NEGLATIPACWWWAT369
KCNS3GATLRHSYHEVGLLLLFLSVGISIFSVLIY>S<VEKDD---------HTSSLTSIPICWWWAT365
KCNV1GMTITQCYEEVGLLLLFLSVGISIFSTVEY>F<AEQSI---------PDTTFTSVPCAWWWAT387
KCNV2GFTLRQCYQQVGCLLLFIAMGIFTFSAAVY>S<VEHDV---------PSTNFTTIPHSWWWAA452
cons                              > <                              

See full Alignment of Paralogues


Known Variants in KCNQ1

ProteinCDSDisease ClassificationDiseasedbSNP linksEffect Prediction
p.L282Pc.845T>C Inherited ArrhythmiaLQTSSIFT: deleterious
Polyphen: probably damaging
ReportsInherited ArrhythmiaLQTS Spectrum and prevalence of mutations from the first 2,500 consecutive unrelated patients referred for the FAMILION long QT syndrome genetic test. Heart Rhythm. 2009 6(9):1297-303. 19716085