Paralogue Annotation for KCNQ1 residue 146

Residue details

Gene: KCNQ1
Reference Sequences: LRG: LRG_287, Ensembl variant: ENST00000155840 / ENSP00000155840
Amino Acid Position: 146
Reference Amino Acid: E - Glutamate
Protein Domain: Transmembrane/Linker/Pore


Paralogue Variants mapped to KCNQ1 residue 146

No paralogue variants have been mapped to residue 146 for KCNQ1.



KCNQ1PT-GWKCFVYHFAVFLIVLVCLIFSVLSTI>E<QYA---------------------------149
KCNQ2PR-G-WAFIYHAYVFLLVFSCLVLSVFSTI>K<EYE---------------------------119
KCNQ3PR-G-WALLYHALVFLIVLGCLILAVLTTF>K<EYE---------------------------149
KCNQ4PR-G-WAFVYHVFIFLLVFSCLVLSVLSTI>Q<EHQ---------------------------125
KCNQ5PR-G-WAFIYHAFVFLLVFGCLILSVFSTI>P<EHT---------------------------153
KCNA1PESSGPARVIAIVSVMVILISIVIFCLETL>P<ELKDDK-DF--------TG-----------200
KCNA10PESSSAARAVAVVSVLVVVISITIFCLETL>P<EFREDR-EL--------KV-----------249
KCNA2PESSGPARIIAIVSVMVILISIVSFCLETL>P<IFRDEN-ED--------MHGSG---V----200
KCNA3PESSGPARGIAIVSVLVILISIVIFCLETL>P<EFRDEK-DY--------PA-ST---SQD--272
KCNA4PESSSPARGIAIVSVLVILISIVIFCLETL>P<EFRDDR-DL--------VM-AL---SAG--345
KCNA5PESSGSARAIAIVSVLVILISIITFCLETL>P<EFRDER-ELLRHPPAP---------HQPPA293
KCNA6PESSGPARGIAIVSVLVILISIVIFCLETL>P<QFRVDG-RGGNNGGVSRVS-PVSRGSQEEE225
KCNA7PESSQAARVLAVVSVLVILVSIVVFCLETL>P<DFRDDR-DGTGL-----AA-AA---AAG--184
KCNB1PNSSVAAKILAIISIMFIVLSTIALSLNTL>P<ELQSLD-EF--------GQ-----------222
KCNB2PNSSVAAKILAIVSILFIVLSTIALSLNTL>P<ELQETD-EF--------GQ-----------226
KCNC1PYSSRYARYVAFASLFFILVSITTFCLETH>E<RFNPIV-NK--------TE-I----E----225
KCNC2PYSSRAARFIAFASLFFILVSITTFCLETH>E<AFNI---VK--------NK-T----E----262
KCNC3PYSSRAARYVAFASLFFILISITTFCLETH>E<GFIHIS-NK--------TV-T----QA---326
KCNC4PYSSRAARVVAFASLFFILVSITTFCLETH>E<AFNI---DR-NV-----TE-I----L----261
KCND1PHTSTAALVFYYVTGFFIAVSVIANVVETI>P<CRGSAR-RS--------SR-----------219
KCND2PHTSTMALVFYYVTGFFIAVSVIANVVETV>P<CGS-SP-GH--------IK-----------217
KCND3PHTSTLALVFYYVTGFFIAVSVITNVVETV>P<CGT-VP-G---------SK-----------214
KCNF1PESSCPARVVAVLSFLLILVSSVVMCMGTI>P<ELQVLD-AE--------GN-----------215
KCNG1PHSGLPGKVFACLSVLFVTVTAVNLSVSTL>P<SLREEEE-Q--------GH-----------260
KCNG2PHSGLAGKLFACVSVSFVAVTAVGLCLSTM>P<DIRAEEE-R--------GE-----------210
KCNG3PTSSLAAQILASVSVVFVIVSMVVLCASTL>P<DWRN-AAAD--------NR-----------204
KCNG4PQSGLPGKVFACLSILFVATTAVSLCVSTM>P<DLRAEED-Q--------GE-----------254
KCNS1PGYSLPSKLFSCVSISVVLASIAAMCIHSL>P<EYQARE-AA--------AA-----------253
KCNS2PGYSVLSRVFSILSILVVMGSIITMCLNSL>P<DFQIPD-SQ--------GN-----------220
KCNS3PAYCLSAKLIAISSLSVVLASIVAMCVHSM>S<EFQNED-GE---------------------216
KCNV1PGSSTAARIFGVISIIFVVVSIINMALMSA>E<L-----------------S-----------235
KCNV2PFSSVAAKAIGVASSTFVLVSVVALALNTV>E<EMQQHS-GQ--------GE-----------293
cons                              > <                              

See full Alignment of Paralogues


Known Variants in KCNQ1

ProteinCDSDisease ClassificationDiseasedbSNP linksEffect Prediction
p.E146Kc.436G>A Inherited ArrhythmiaLQTSSIFT: tolerated
Polyphen: possibly damaging
ReportsInherited ArrhythmiaLQTS Genetic testing in the long QT syndrome: development and validation of an efficient approach to genotyping in clinical practice. JAMA. 2005 294(23):2975-80. 16414944
Inherited ArrhythmiaLQTS Posthumous diagnosis of long QT syndrome from neonatal screening cards. Heart Rhythm. 2010 7(4):481-6. 20167303
p.E146Gc.437A>G Inherited ArrhythmiaLQTSSIFT:
Polyphen:
ReportsInherited ArrhythmiaLQTS Syncope and cardiac arrest during strenuous exercise associated with a novel mutation in LQTS1. Clin Case Rep. 2015 3(12):971-4. doi: 10.1002/ccr3.394. eCollection 20 26734131