Paralogue Annotation for KCNQ1 residue 170

Residue details

Gene: KCNQ1
Reference Sequences: LRG: LRG_287, Ensembl variant: ENST00000155840 / ENSP00000155840
Amino Acid Position: 170
Reference Amino Acid: E - Glutamate
Protein Domain: Transmembrane/Linker/Pore


Paralogue Variants mapped to KCNQ1 residue 170

No paralogue variants have been mapped to residue 170 for KCNQ1.



KCNQ1--------ALATGT-LF-WMEIVLVVFFGT>E<YVVRLWSAGCRSKYVGLWGRLRFARKPISI200
KCNQ2--------KSSEGA-LY-ILEIVTIVVFGV>E<YFVRIWAAGCCCRYRGWRGRLKFARKPFCV170
KCNQ3--------TVSGDW-LL-LLETFAIFIFGA>E<FALRIWAAGCCCRYKGWRGRLKFARKPLCM200
KCNQ4--------ELANEC-LL-ILEFVMIVVFGL>E<YIVRVWSAGCCCRYRGWQGRFRFARKPFCV176
KCNQ5--------KLASSC-LL-ILEFVMIVVFGL>E<FIIRIWSAGCCCRYRGWQGRLRFARKPFCV204
KCNA1NTTVIYNSNIFTDP-FF-IVETLCIIWFSF>E<LVVR---------FFACPSKTDFFKNIMNF256
KCNA10MSKTVLSQTMFTDP-FF-MVESTCIVWFTF>E<LVLR---------FVVCPSKTDFFRNIMNI306
KCNA2STIGYQQSTSFTDP-FF-IVETLCIIWFSF>E<FLVR---------FFACPSKAGFFTNIMNI257
KCNA3TSGSRAGASSFSDP-FF-VVETLCIIWFSF>E<LLVR---------FFACPSKATFSRNIMNL330
KCNA4PHLENSGHTIFNDP-FF-IVETVCIVWFSF>E<FVVR---------CFACPSQALFFKNIMNI406
KCNA5PTVAPLLPRTLADP-FF-IVETTCVIWFTF>E<LLVR---------FFACPSKAGFSRNIMNI359
KCNA6SSLSTLGGSFFTDP-FF-LVETLCIVWFTF>E<LLVR---------FSACPSKPAFFRNIMNI298
KCNA7QMPGNPPRLPFNDP-FF-VVETLCICWFSF>E<LLVR---------LLVCPSKAIFFKNVMNL244
KCNB1---------STDNPQLA-HVEAVCIAWFTM>E<YLLR---------FLSSPKKWKFFKGPLNA264
KCNB2---------LNDNRQLA-HVEAVCIAWFTM>E<YLLR---------FLSSPNKWKFFKGPLNV268
KCNC1GTQVRYYREAETEA-FLTYIEGVCVVWFTF>E<FLMR---------VIFCPNKVEFIKNSLNI280
KCNC2GTSVVLQYEIETDP-ALTYVEGVCVVWFTF>E<FLVR---------IVFSPNKLEFIKNLLNI317
KCNC3PPENITNVEVETEP-FLTYVEGVCVVWFTF>E<FLMR---------ITFCPDKVEFLKSSLNI383
KCNC4ITSVHFRREVETEP-ILTYIEGVCVLWFTL>E<FLVR---------IVCCPDTLDFVKNLLNI316
KCND1---EQPCGERFPQA-FF-CMDTACVLIFTG>E<YLLR---------LFAAPSRCRFLRSVMSL266
KCND2---ELPCGERYAVA-FF-CLDTACVMIFTV>E<YLLR---------LAAAPSRYRFVRSVMSI264
KCND3---ELPCGERYSVA-FF-CLDTACVMIFTV>E<YLLR---------LFAAPSRYRFIRSVMSI261
KCNF1---------RVEHPTLE-NVETACIGWFTL>E<YLLR---------LFSSPNKLHFALSFMNI257
KCNG1--------SQMCHN-VF-IVESVCVGWFSL>E<FLLR---------LIQAPSKFAFLRSPLTL303
KCNG2--------SPKCRS-LF-VLETVCVAWFSF>E<FLLR---------SLQAESKCAFLRAPLNI253
KCNG3DDRSRYSAGPGREP-SG-IIEAICIGWFTA>E<CIVR---------FIVSKNKCEFVKRPLNI256
KCNG4--------SRKCYY-IF-IVETICVAWFSL>E<FCLR---------FVQAQDKCQFFQGPLNI297
KCNS1VAAGRSPEGVRDDPVLR-RLEYFCIAWFSF>E<VSSR---------LLLAPSTRNFFCHPLNL307
KCNS2---------PGEDPRFE-IVEHFGIAWFTF>E<LVAR---------FAVAPDFLKFFKNALNL262
KCNS3----------VDDPVLE-GVEIACIAWFTG>E<LAVR---------LAAAPCQKKFWKNPLNI257
KCNV1---------WLDLQLLE-ILEYVCISWFTG>E<FVLR---------FLCVRDRCRFLRKVPNI277
KCNV2--------GPDLRPILE-HVEMLCMGFFTL>E<YLLR---------LASTPDLRRFARSALNL337
cons                              > <                              

See full Alignment of Paralogues


Known Variants in KCNQ1

ProteinCDSDisease ClassificationDiseasedbSNP linksEffect Prediction
p.E170Gc.509A>G Inherited ArrhythmiaLQTSSIFT:
Polyphen:
ReportsInherited ArrhythmiaLQTS Founder mutations characterise the mutation panorama in 200 Swedish index cases referred for Long QT syndrome genetic testing. BMC Cardiovasc Disord. 2012 12:95. doi: 10.1186/1471-2261-12-95. 23098067