Paralogue Annotation for KCNQ1 residue 169

Residue details

Gene: KCNQ1
Reference Sequences: LRG: LRG_287, Ensembl variant: ENST00000155840 / ENSP00000155840
Amino Acid Position: 169
Reference Amino Acid: T - Threonine
Protein Domain: Transmembrane/Linker/Pore


Paralogue Variants mapped to KCNQ1 residue 169

No paralogue variants have been mapped to residue 169 for KCNQ1.



KCNQ1---------ALATGT-LF-WMEIVLVVFFG>T<EYVVRLWSAGCRSKYVGLWGRLRFARKPIS199
KCNQ2---------KSSEGA-LY-ILEIVTIVVFG>V<EYFVRIWAAGCCCRYRGWRGRLKFARKPFC169
KCNQ3---------TVSGDW-LL-LLETFAIFIFG>A<EFALRIWAAGCCCRYKGWRGRLKFARKPLC199
KCNQ4---------ELANEC-LL-ILEFVMIVVFG>L<EYIVRVWSAGCCCRYRGWQGRFRFARKPFC175
KCNQ5---------KLASSC-LL-ILEFVMIVVFG>L<EFIIRIWSAGCCCRYRGWQGRLRFARKPFC203
KCNA1-NTTVIYNSNIFTDP-FF-IVETLCIIWFS>F<ELVVR---------FFACPSKTDFFKNIMN255
KCNA10NMSKTVLSQTMFTDP-FF-MVESTCIVWFT>F<ELVLR---------FVVCPSKTDFFRNIMN305
KCNA2NSTIGYQQSTSFTDP-FF-IVETLCIIWFS>F<EFLVR---------FFACPSKAGFFTNIMN256
KCNA3STSGSRAGASSFSDP-FF-VVETLCIIWFS>F<ELLVR---------FFACPSKATFSRNIMN329
KCNA4APHLENSGHTIFNDP-FF-IVETVCIVWFS>F<EFVVR---------CFACPSQALFFKNIMN405
KCNA5GPTVAPLLPRTLADP-FF-IVETTCVIWFT>F<ELLVR---------FFACPSKAGFSRNIMN358
KCNA6SSSLSTLGGSFFTDP-FF-LVETLCIVWFT>F<ELLVR---------FSACPSKPAFFRNIMN297
KCNA7SQMPGNPPRLPFNDP-FF-VVETLCICWFS>F<ELLVR---------LLVCPSKAIFFKNVMN243
KCNB1----------STDNPQLA-HVEAVCIAWFT>M<EYLLR---------FLSSPKKWKFFKGPLN263
KCNB2----------LNDNRQLA-HVEAVCIAWFT>M<EYLLR---------FLSSPNKWKFFKGPLN267
KCNC1NGTQVRYYREAETEA-FLTYIEGVCVVWFT>F<EFLMR---------VIFCPNKVEFIKNSLN279
KCNC2NGTSVVLQYEIETDP-ALTYVEGVCVVWFT>F<EFLVR---------IVFSPNKLEFIKNLLN316
KCNC3APPENITNVEVETEP-FLTYVEGVCVVWFT>F<EFLMR---------ITFCPDKVEFLKSSLN382
KCNC4NITSVHFRREVETEP-ILTYIEGVCVLWFT>L<EFLVR---------IVCCPDTLDFVKNLLN315
KCND1----EQPCGERFPQA-FF-CMDTACVLIFT>G<EYLLR---------LFAAPSRCRFLRSVMS265
KCND2----ELPCGERYAVA-FF-CLDTACVMIFT>V<EYLLR---------LAAAPSRYRFVRSVMS263
KCND3----ELPCGERYSVA-FF-CLDTACVMIFT>V<EYLLR---------LFAAPSRYRFIRSVMS260
KCNF1----------RVEHPTLE-NVETACIGWFT>L<EYLLR---------LFSSPNKLHFALSFMN256
KCNG1---------SQMCHN-VF-IVESVCVGWFS>L<EFLLR---------LIQAPSKFAFLRSPLT302
KCNG2---------SPKCRS-LF-VLETVCVAWFS>F<EFLLR---------SLQAESKCAFLRAPLN252
KCNG3-DDRSRYSAGPGREP-SG-IIEAICIGWFT>A<ECIVR---------FIVSKNKCEFVKRPLN255
KCNG4---------SRKCYY-IF-IVETICVAWFS>L<EFCLR---------FVQAQDKCQFFQGPLN296
KCNS1AVAAGRSPEGVRDDPVLR-RLEYFCIAWFS>F<EVSSR---------LLLAPSTRNFFCHPLN306
KCNS2----------PGEDPRFE-IVEHFGIAWFT>F<ELVAR---------FAVAPDFLKFFKNALN261
KCNS3-----------VDDPVLE-GVEIACIAWFT>G<ELAVR---------LAAAPCQKKFWKNPLN256
KCNV1----------WLDLQLLE-ILEYVCISWFT>G<EFVLR---------FLCVRDRCRFLRKVPN276
KCNV2---------GPDLRPILE-HVEMLCMGFFT>L<EYLLR---------LASTPDLRRFARSALN336
cons                              > <                              

See full Alignment of Paralogues


Known Variants in KCNQ1

ProteinCDSDisease ClassificationDiseasedbSNP linksEffect Prediction
p.T169Rc.506C>G Inherited ArrhythmiaLQTSSIFT: deleterious
Polyphen: possibly damaging
ReportsInherited ArrhythmiaLQTS The genetic basis of long QT and short QT syndromes: a mutation update. Hum Mutat. 2009 30(11):1486-511. 19862833
Inherited ArrhythmiaLQTS RNA splicing. The human splicing code reveals new insights into the genetic determinants of disease. Science. 2015 347(6218):1254806. doi: 10.1126/science.1254806. 25525159
p.T169Mc.506C>T Putative BenignSIFT:
Polyphen: