Paralogue Annotation for KCNQ1 residue 236

Residue details

Gene: KCNQ1
Reference Sequences: LRG: LRG_287, Ensembl variant: ENST00000155840 / ENSP00000155840
Amino Acid Position: 236
Reference Amino Acid: L - Leucine
Protein Domain: Transmembrane/Linker/Pore


Paralogue Variants mapped to KCNQ1 residue 236

No paralogue variants have been mapped to residue 236 for KCNQ1.



KCNQ1-----------SKGQVFATSAIRGIRFLQI>L<RMLHVDRQGGTWRLLGSVVFIHRQELITTL266
KCNQ2-----------SQGNVFATSALRSLRFLQI>L<RMIRMDRRGGTWKLLGSVVYAHSKELVTAW236
KCNQ3-----------NQGNVLA-TSLRSLRFLQI>L<RMLRMDRRGGTWKLLGSAICAHSKELITAW265
KCNQ4-----------TQGNIFATSALRSMRFLQI>L<RMVRMDRRGGTWKLLGSVVYAHSKELITAW242
KCNQ5-----------TQGNIFATSALRSLRFLQI>L<RMVRMDRRGGTWKLLGSVVYAHSKELITAW270
KCNA1G-------N-QKGEQATSLAILRVIRLVRV>F<RIFKLSRHSKGLQILGQTLKASMRELGLLI330
KCNA10EP---------SAQQNMSLAILRIIRLVRV>F<RIFKLSRHSKGLQILGQTLKASMRELGLLI379
KCNA2E-------DAQQGQQAMSLAILRVIRLVRV>F<RIFKLSRHSKGLQILGQTLKASMRELGLLI332
KCNA3----------GNGQQAMSLAILRVIRLVRV>F<RIFKLSRHSKGLQILGQTLKASMRELGLLI402
KCNA4GG------GNGQQQQAMSFAILRIIRLVRV>F<RIFKLSRHSKGLQILGHTLRASMRELGLLI482
KCNA5---PGGGGGGQNGQQAMSLAILRVIRLVRV>F<RIFKLSRHSKGLQILGKTLQASMRELGLLI438
KCNA6EQQPASGGGGQNGQQAMSLAILRVIRLVRV>F<RIFKLSRHSKGLQILGKTLQASMRELGLLI380
KCNA7----------GVGQQAMSLAILRVIRLVRV>F<RIFKLSRHSKGLQILGQTLRASMRELGLLI316
KCNB1N--------KSVLQFQNVRRVVQIFRIMRI>L<RILKLARHSTGLQSLGFTLRRSYNELGLLI335
KCNB2N--------KSVLQFQNVRRVVQIFRIMRI>L<RILKLARHSTGLQSLGFTLRRSYNELGLLI339
KCNC1---------LSSKAAKDVLGFLRVVRFVRI>L<RIFKLTRHFVGLRVLGHTLRASTNEFLLLI349
KCNC2---------LSSKAAKDVLGFLRVVRFVRI>L<RIFKLTRHFVGLRVLGHTLRASTNEFLLLI386
KCNC3---------LSSKAAKDVLGFLRVVRFVRI>L<RIFKLTRHFVGLRVLGHTLRASTNEFLLLI452
KCNC4---------LSSKAARDVLGFLRVVRFVRI>L<RIFKLTRHFVGLRVLGHTLRASTNEFLLLI385
KCND1-------------KNDDVSGAFVTLRVFRV>F<RIFKFSRHSQGLRILGYTLKSCASELGFLL330
KCND2-------------DNEDVSGAFVTLRVFRV>F<RIFKFSRHSQGLRILGYTLKSCASELGFLL328
KCND3-------------NNEDVSGAFVTLRVFRV>F<RIFKFSRHSQGLRILGYTLKSCASELGFLL325
KCNF1--------GARMMELTNVQQAVQALRIMRI>A<RIFKLARHSSGLQTLTYALKRSFKELGLLL328
KCNG1RR----KPGAGNSYLDKVGLVLRVLRALRI>L<YVMRLARHSLGLQTLGLTARRCTREFGLLL381
KCNG2-A----AGPGGTKLLERAGLVLRLLRALRV>L<YVMRLARHSLGLRSLGLTMRRCAREFGLLL326
KCNG3-------FTGENSQLQRAGVTLRVLRMMRI>F<WVIKLARHFIGLQTLGLTLKRCYREMVMLL327
KCNG4DG----ERPSGSSYLEKVGLVLRVLRALRI>L<YVMRLARHSLGLQTLGLTVRRCTREFGLLL375
KCNS1D--------QGGKEFGHLGKVVQVFRLMRI>F<RVLKLARHSTGLRSLGATLKHSYREVGILL380
KCNS2V--------ESTPTLANLGRVAQVLRLMRI>F<RILKLARHSTGLRSLGATLKYSYKEVGLLL333
KCNS3E--------EESEDIENMGKVVQILRLMRI>F<RILKLARHSVGLRSLGATLRHSYHEVGLLL328
KCNV1S--------QTTQELENVGRIVQVLRLLRA>L<RMLKLGRHSTGLRSLGMTITQCYEEVGLLL350
KCNV2GH----QRGQTVGSVGKVGQVLRVMRLMRI>F<RILKLARHSTGLRAFGFTLRQCYQQVGCLL415
cons                              > <                              

See full Alignment of Paralogues


Known Variants in KCNQ1

ProteinCDSDisease ClassificationDiseasedbSNP linksEffect Prediction
p.L236Rc.707T>G Inherited ArrhythmiaLQTSSIFT:
Polyphen:
ReportsInherited ArrhythmiaLQTS High incidence of functional ion-channel abnormalities in a consecutive Long QT cohort with novel missense genetic variants of unknown significance. Sci Rep. 2015 5:10009. doi: 10.1038/srep10009. 26066609
p.Leu236Proc.707T>C UnknownSIFT:
Polyphen: