Paralogue Annotation for KCNQ1 residue 132

Residue details

Gene: KCNQ1
Reference Sequences: LRG: LRG_287, Ensembl variant: ENST00000155840 / ENSP00000155840
Amino Acid Position: 132
Reference Amino Acid: I - Isoleucine
Protein Domain: Transmembrane/Linker/Pore


Paralogue Variants mapped to KCNQ1 residue 132

No paralogue variants have been mapped to residue 132 for KCNQ1.



KCNQ1---VQGRVYNFLERPT-GWKCFVYHFAVFL>I<VLVCLIFSVLSTIEQYA-------------149
KCNQ2---LQNFLYNVLERPR-G-WAFIYHAYVFL>L<VFSCLVLSVFSTIKEYE-------------119
KCNQ3---IQTLIYDALERPR-G-WALLYHALVFL>I<VLGCLILAVLTTFKEYE-------------149
KCNQ4---LQNWVYNVLERPR-G-WAFVYHVFIFL>L<VFSCLVLSVLSTIQEHQ-------------125
KCNQ5---VQNYLYNVLERPR-G-WAFIYHAFVFL>L<VFGCLILSVFSTIPEHT-------------153
KCNA1EKEYQRQVWLLFEYPESSGPARVIAIVSVM>V<ILISIVIFCLETLPELKDDK-DF-------198
KCNA10TNDIHRQFWLLFEYPESSSAARAVAVVSVL>V<VVISITIFCLETLPEFREDR-EL-------247
KCNA2ENEFQRQVWLLFEYPESSGPARIIAIVSVM>V<ILISIVSFCLETLPIFRDEN-ED-------194
KCNA3RRDFQRQVWLLFEYPESSGPARGIAIVSVL>V<ILISIVIFCLETLPEFRDEK-DY-------265
KCNA4ENEFKKQIWLLFEYPESSSPARGIAIVSVL>V<ILISIVIFCLETLPEFRDDR-DL-------338
KCNA5RNEFQRQVWLIFEYPESSGSARAIAIVSVL>V<ILISIITFCLETLPEFRDER-ELLRHPPAP288
KCNA6SQPFQRQVWLLFEYPESSGPARGIAIVSVL>V<ILISIVIFCLETLPQFRVDG-RGGNNGGVS212
KCNA7RRAFARQLWLLFEFPESSQAARVLAVVSVL>V<ILVSIVVFCLETLPDFRDDR-DGTGL----177
KCNB1CAEKRKKLWDLLEKPNSSVAAKILAIISIM>F<IVLSTIALSLNTLPELQSLD-EF-------220
KCNB2CPDKRKKLWDLLEKPNSSVAAKILAIVSIL>F<IVLSTIALSLNTLPELQETD-EF-------224
KCNC1WRRWQPRIWALFEDPYSSRYARYVAFASLF>F<ILVSITTFCLETHERFNPIV-NK-------221
KCNC2WRRLQPRMWALFEDPYSSRAARFIAFASLF>F<ILVSITTFCLETHEAFNI---VK-------258
KCNC3WRRWQPRVWALFEDPYSSRAARYVAFASLF>F<ILISITTFCLETHEGFIHIS-NK-------321
KCNC4CRGWQPRMWALFEDPYSSRAARVVAFASLF>F<ILVSITTFCLETHEAFNI---DR-NV----257
KCND1GSSLRQRLWRAFENPHTSTAALVFYYVTGF>F<IAVSVIANVVETIPCRGSAR-RS-------217
KCND2MT-ARQRVWRAFENPHTSTMALVFYYVTGF>F<IAVSVIANVVETVPCGS-SP-GH-------215
KCND3LS-FRQTMWRAFENPHTSTLALVFYYVTGF>F<IAVSVITNVVETVPCGT-VP-G--------212
KCNF1WRRCQKCVWKFLEKPESSCPARVVAVLSFL>L<ILVSSVVMCMGTIPELQVLD-AE-------213
KCNG1GR-CMRRLRDMVERPHSGLPGKVFACLSVL>F<VTVTAVNLSVSTLPSLREEEE-Q-------258
KCNG2QR-GRRRLRDVVDNPHSGLAGKLFACVSVS>F<VAVTAVGLCLSTMPDIRAEEE-R-------208
KCNG3SRRWLERMRRTFEEPTSSLAAQILASVSVV>F<VIVSMVVLCASTLPDWRN-AAAD-------202
KCNG4GL-CMNRLREMVENPQSGLPGKVFACLSIL>F<VATTAVSLCVSTMPDLRAEED-Q-------252
KCNS1CGRLRRRLWLTMENPGYSLPSKLFSCVSIS>V<VLASIAAMCIHSLPEYQARE-AA-------251
KCNS2LGNFRRQLWLALDNPGYSVLSRVFSILSIL>V<VMGSIITMCLNSLPDFQIPD-SQ-------218
KCNS3FGQLRKKIWIRMENPAYCLSAKLIAISSLS>V<VLASIVAMCVHSMSEFQNED-GE-------216
KCNV1CPTVRQKLWNILEKPGSSTAARIFGVISII>F<VVVSIINMALMSAEL---------------234
KCNV2YGPQRRRLWNLMEKPFSSVAAKAIGVASST>F<VLVSVVALALNTVEEMQQHS-GQ-------291
cons                              > <                              

See full Alignment of Paralogues


Known Variants in KCNQ1

ProteinCDSDisease ClassificationDiseasedbSNP linksEffect Prediction
p.I132Lc.394A>C Inherited ArrhythmiaLQTSSIFT: tolerated
Polyphen: benign
ReportsInherited ArrhythmiaLQTS The genetic basis of long QT and short QT syndromes: a mutation update. Hum Mutat. 2009 30(11):1486-511. 19862833