Paralogue Annotation for KCNQ1 residue 194

Residue details

Gene: KCNQ1
Reference Sequences: LRG: LRG_287, Ensembl variant: ENST00000155840 / ENSP00000155840
Amino Acid Position: 194
Reference Amino Acid: A - Alanine
Protein Domain: Transmembrane/Linker/Pore


Paralogue Variants mapped to KCNQ1 residue 194

No paralogue variants have been mapped to residue 194 for KCNQ1.



KCNQ1VVFFGTEYVVRLWSAGCRSKYVGLWGRLRF>A<RKPISIIDLIVVVASMVVLCVG--------216
KCNQ2IVVFGVEYFVRIWAAGCCCRYRGWRGRLKF>A<RKPFCVIDIMVLIASIAVLAAG--------186
KCNQ3IFIFGAEFALRIWAAGCCCRYKGWRGRLKF>A<RKPLCMLDIFVLIASVPVVAVG--------216
KCNQ4IVVFGLEYIVRVWSAGCCCRYRGWQGRFRF>A<RKPFCVIDFIVFVASVAVIAAG--------192
KCNQ5IVVFGLEFIIRIWSAGCCCRYRGWQGRLRF>A<RKPFCVIDTIVLIASIAVVSAK--------220
KCNA1IIWFSFELVVR---------FFACPSKTDF>F<KNIMNFIDIVAIIPYFITLGTEIAEQEG--278
KCNA10IVWFTFELVLR---------FVVCPSKTDF>F<RNIMNIIDIISIIPYFATLITELVQETEP-329
KCNA2IIWFSFEFLVR---------FFACPSKAGF>F<TNIMNIIDIVAIIPYFITLGTELAEKPE--279
KCNA3IIWFSFELLVR---------FFACPSKATF>S<RNIMNLIDIVAIIPYFITLGTELAERQ---351
KCNA4IVWFSFEFVVR---------CFACPSQALF>F<KNIMNIIDIVSILPYFITLGTDLAQQQGG-429
KCNA5VIWFTFELLVR---------FFACPSKAGF>S<RNIMNIIDVVAIFPYFITLGTELAEQQ---380
KCNA6IVWFTFELLVR---------FSACPSKPAF>F<RNIMNIIDLVAIFPYFITLGTELVQQQEQQ322
KCNA7ICWFSFELLVR---------LLVCPSKAIF>F<KNVMNLIDFVAILPYFVALGTELARQR---265
KCNB1IAWFTMEYLLR---------FLSSPKKWKF>F<KGPLNAIDLLAILPYYVTIFLTES---N--283
KCNB2IAWFTMEYLLR---------FLSSPNKWKF>F<KGPLNVIDLLAILPYYVTIFLTES---N--287
KCNC1VVWFTFEFLMR---------VIFCPNKVEF>I<KNSLNIIDFVAILPFYLEVGLSG-------297
KCNC2VVWFTFEFLVR---------IVFSPNKLEF>I<KNLLNIIDFVAILPFYLEVGLSG-------334
KCNC3VVWFTFEFLMR---------ITFCPDKVEF>L<KSSLNIIDCVAILPFYLEVGLSG-------400
KCNC4VLWFTLEFLVR---------IVCCPDTLDF>V<KNLLNIIDFVAILPFYLEVGLSG-------333
KCND1VLIFTGEYLLR---------LFAAPSRCRF>L<RSVMSLIDVVAILPYYIGLLVP--------282
KCND2VMIFTVEYLLR---------LAAAPSRYRF>V<RSVMSIIDVVAILPYYIGLVMT--------280
KCND3VMIFTVEYLLR---------LFAAPSRYRF>I<RSVMSIIDVVAIMPYYIGLVMT--------277
KCNF1IGWFTLEYLLR---------LFSSPNKLHF>A<LSFMNIVDVLAILPFYVSLTLTHL------275
KCNG1VGWFSLEFLLR---------LIQAPSKFAF>L<RSPLTLIDLVAILPYYITLLVDGAAAGRR-326
KCNG2VAWFSFEFLLR---------SLQAESKCAF>L<RAPLNIIDILALLPFYVSLLLGL-----A-271
KCNG3IGWFTAECIVR---------FIVSKNKCEF>V<KRPLNIIDLLAITPYYISVLMTV-------273
KCNG4VAWFSLEFCLR---------FVQAQDKCQF>F<QGPLNIIDILAISPYYVSLAVSEEPPEDG-320
KCNS1IAWFSFEVSSR---------LLLAPSTRNF>F<CHPLNLIDIVSVLPFYLTLLAGVALG-D--328
KCNS2IAWFTFELVAR---------FAVAPDFLKF>F<KNALNLIDLMSIVPFYITLVVNLV---V--281
KCNS3IAWFTGELAVR---------LAAAPCQKKF>W<KNPLNIIDFVSIIPFYATLAVDTK---E--276
KCNV1ISWFTGEFVLR---------FLCVRDRCRF>L<RKVPNIIDLLAILPFYITLLVESLSG-S--298
KCNV2MGFFTLEYLLR---------LASTPDLRRF>A<RSALNLVDLVAILPLYLQLLLECFTGEGH-360
cons                              > <                              

See full Alignment of Paralogues


Known Variants in KCNQ1

ProteinCDSDisease ClassificationDiseasedbSNP linksEffect Prediction
p.A194Pc.580G>C Inherited ArrhythmiaLQTSSIFT: deleterious
Polyphen: probably damaging
ReportsInherited ArrhythmiaLQTS Spectrum of mutations in long-QT syndrome genes. KVLQT1, HERG, SCN5A, KCNE1, and KCNE2. Circulation. 2000 102(10):1178-85. 10973849