Paralogue Annotation for KCNQ1 residue 137

Residue details

Gene: KCNQ1
Reference Sequences: LRG: LRG_287, Ensembl variant: ENST00000155840 / ENSP00000155840
Amino Acid Position: 137
Reference Amino Acid: L - Leucine
Protein Domain: Transmembrane/Linker/Pore


Paralogue Variants mapped to KCNQ1 residue 137

No paralogue variants have been mapped to residue 137 for KCNQ1.



KCNQ1GRVYNFLERPT-GWKCFVYHFAVFLIVLVC>L<IFSVLSTIEQYA------------------149
KCNQ2NFLYNVLERPR-G-WAFIYHAYVFLLVFSC>L<VLSVFSTIKEYE------------------119
KCNQ3TLIYDALERPR-G-WALLYHALVFLIVLGC>L<ILAVLTTFKEYE------------------149
KCNQ4NWVYNVLERPR-G-WAFVYHVFIFLLVFSC>L<VLSVLSTIQEHQ------------------125
KCNQ5NYLYNVLERPR-G-WAFIYHAFVFLLVFGC>L<ILSVFSTIPEHT------------------153
KCNA1RQVWLLFEYPESSGPARVIAIVSVMVILIS>I<VIFCLETLPELKDDK-DF--------TG--200
KCNA10RQFWLLFEYPESSSAARAVAVVSVLVVVIS>I<TIFCLETLPEFREDR-EL--------KV--249
KCNA2RQVWLLFEYPESSGPARIIAIVSVMVILIS>I<VSFCLETLPIFRDEN-ED--------MHGS198
KCNA3RQVWLLFEYPESSGPARGIAIVSVLVILIS>I<VIFCLETLPEFRDEK-DY--------PA-S268
KCNA4KQIWLLFEYPESSSPARGIAIVSVLVILIS>I<VIFCLETLPEFRDDR-DL--------VM-A341
KCNA5RQVWLIFEYPESSGSARAIAIVSVLVILIS>I<ITFCLETLPEFRDER-ELLRHPPAP-----288
KCNA6RQVWLLFEYPESSGPARGIAIVSVLVILIS>I<VIFCLETLPQFRVDG-RGGNNGGVSRVS-P216
KCNA7RQLWLLFEFPESSQAARVLAVVSVLVILVS>I<VVFCLETLPDFRDDR-DGTGL-----AA-A180
KCNB1KKLWDLLEKPNSSVAAKILAIISIMFIVLS>T<IALSLNTLPELQSLD-EF--------GQ--222
KCNB2KKLWDLLEKPNSSVAAKILAIVSILFIVLS>T<IALSLNTLPELQETD-EF--------GQ--226
KCNC1PRIWALFEDPYSSRYARYVAFASLFFILVS>I<TTFCLETHERFNPIV-NK--------TE-I224
KCNC2PRMWALFEDPYSSRAARFIAFASLFFILVS>I<TTFCLETHEAFNI---VK--------NK-T261
KCNC3PRVWALFEDPYSSRAARYVAFASLFFILIS>I<TTFCLETHEGFIHIS-NK--------TV-T324
KCNC4PRMWALFEDPYSSRAARVVAFASLFFILVS>I<TTFCLETHEAFNI---DR-NV-----TE-I260
KCND1QRLWRAFENPHTSTAALVFYYVTGFFIAVS>V<IANVVETIPCRGSAR-RS--------SR--219
KCND2QRVWRAFENPHTSTMALVFYYVTGFFIAVS>V<IANVVETVPCGS-SP-GH--------IK--217
KCND3QTMWRAFENPHTSTLALVFYYVTGFFIAVS>V<ITNVVETVPCGT-VP-G---------SK--214
KCNF1KCVWKFLEKPESSCPARVVAVLSFLLILVS>S<VVMCMGTIPELQVLD-AE--------GN--215
KCNG1RRLRDMVERPHSGLPGKVFACLSVLFVTVT>A<VNLSVSTLPSLREEEE-Q--------GH--260
KCNG2RRLRDVVDNPHSGLAGKLFACVSVSFVAVT>A<VGLCLSTMPDIRAEEE-R--------GE--210
KCNG3ERMRRTFEEPTSSLAAQILASVSVVFVIVS>M<VVLCASTLPDWRN-AAAD--------NR--204
KCNG4NRLREMVENPQSGLPGKVFACLSILFVATT>A<VSLCVSTMPDLRAEED-Q--------GE--254
KCNS1RRLWLTMENPGYSLPSKLFSCVSISVVLAS>I<AAMCIHSLPEYQARE-AA--------AA--253
KCNS2RQLWLALDNPGYSVLSRVFSILSILVVMGS>I<ITMCLNSLPDFQIPD-SQ--------GN--220
KCNS3KKIWIRMENPAYCLSAKLIAISSLSVVLAS>I<VAMCVHSMSEFQNED-GE------------216
KCNV1QKLWNILEKPGSSTAARIFGVISIIFVVVS>I<INMALMSAEL-----------------S--235
KCNV2RRLWNLMEKPFSSVAAKAIGVASSTFVLVS>V<VALALNTVEEMQQHS-GQ--------GE--293
cons                              > <                              

See full Alignment of Paralogues


Known Variants in KCNQ1

ProteinCDSDisease ClassificationDiseasedbSNP linksEffect Prediction
p.L137Fc.409C>T Inherited ArrhythmiaLQTSSIFT: deleterious
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