Paralogue Annotation for KCNQ1 residue 73

Residue details

Gene: KCNQ1
Reference Sequences: LRG: LRG_287, Ensembl variant: ENST00000155840 / ENSP00000155840
Amino Acid Position: 73
Reference Amino Acid: P - Proline
Protein Domain: N-terminus


Paralogue Variants mapped to KCNQ1 residue 73

No paralogue variants have been mapped to residue 73 for KCNQ1.



KCNQ1YAPIAPGAPGP--------APPASPAAPAA>P<PVASDL---GPRPPVSL------DPRVSIY94
KCNQ2-----A-PK---------------RGSILS>-<---------KPRAGG--AGAGK-PPKRNAF73
KCNQ3---------DEG-----QR---R----TPQ>-<---------GIGL-LAKTPLSRPVKRNNAK103
KCNQ4---RRLGLLGSP-----L------PPGAPL>P<---------GPGSGSGSACGQR-SSAAHKR79
KCNQ5---ATLGGGGGG-----LRESRRGKQGARM>S<---------LLGKPL-SYTSSQ-SCRRNVK107
KCNA1FFDRNRPSFDAILYYYQSGGRLRRPVNVPL>D<MFSEEIKFYELGEEAME----K--FREDEG135
KCNA10FFDRNRPSFDGILYYYQSGGKIRRPANVPI>D<IFADEISFYELGSEAMD----Q--FREDEG184
KCNA2FFDRNRPSFDAILYYYQSGGRLRRPVNVPL>D<IFSEEIRFYELGEEAME----M--FREDEG131
KCNA3FFDRNRPSFDAILYYYQSGGRIRRPVNVPI>D<IFSEEIRFYQLGEEAME----K--FREDEG202
KCNA4FFDRNRPSFDAILYYYQSGGRLKRPVNVPF>D<IFTEEVKFYQLGEEALL----K--FREDEG274
KCNA5FFDRNRPSFDGILYYYQSGGRLRRPVNVSL>D<VFADEIRFYQLGDEAME----R--FREDEG218
KCNA6FFDRNRPSFDAILYYYQSGGRLRRPVNVPL>D<IFLEEIRFYQLGDEALA----A--FREDEG139
KCNA7FFDRHRPSFDAVLYYYQSGGRLRRPAHVPL>D<VFLEEVAFYGLGAAALA----R--LREDEG111
KCNB1FFDRHPGAFTSILNFYRT-GRLHMMEEMCA>L<SFSQELDYWGIDEIYLE----S--CCQARY137
KCNB2FFDRHPGAFTSILNFYRT-GKLHMMEEMCA>L<SFGQELDYWGIDEIYLE----S--CCQARY141
KCNC1FFDRHPGVFAHILNYYRT-GKLHCPADVCG>P<LYEEELAFWGIDETDVE----P--CCWMTY109
KCNC2FFDRHPGVFAYVLNYYRT-GKLHCPADVCG>P<LFEEELAFWGIDETDVE----P--CCWMTY156
KCNC3FFDRHPGVFAYVLNYYRT-GKLHCPADVCG>P<LFEEELGFWGIDETDVE----A--CCWMTY189
KCNC4FFDRHPGVFAYVLNYYRT-GKLHCPADVCG>P<LFEEELTFWGIDETDVE----P--CCWMTY148
KCND1FFDRDPDMFRHVLNFYRT-GRLHCPRQECI>Q<AFDEELAFYGLVPELVG----D--CCLEEY136
KCND2FFDRDPDIFRHILNFYRT-GKLHYPRHECI>S<AYDEELAFFGLIPEIIG----D--CCYEEY137
KCND3FFDRDPEVFRCVLNFYRT-GKLHYPRYECI>S<AYDDELAFYGILPEIIG----D--CCYEEY136
KCNF1YFDRDPDAFKCVIEVYYF-GEVHMKKGICP>I<CFKNEMDFWKVDLKFLD----D--CCKSHL131
KCNG1FFDRNPGAFGTILTFLRA-GKLRLLREMCA>L<SFQEELLYWGIAEDHLD----G--CCKRRY169
KCNG2FFDRSPCAFRAIVALLRA-GKLRLLRGPCA>L<AFRDELAYWGIDEARLE----R--CCLRRL123
KCNG3FFDRHSEAFGFILLYVRGHGKLRFAPRMCE>L<SFYNEMIYWGLEGAHLE----Y--CCQRRL116
KCNG4FFDRSPSAFGVIVSFLAA-GKLVLLQEMCA>L<SFQEELAYWGIEEAHLE----R--CCLRKL165
KCNS1YFDRHPGFFLSLLHFYRT-GHLHVLDELCV>F<AFGQEADYWGLGENALA----A--CCRARY156
KCNS2YFDRNPELFPYVLHFYHT-GKLHVMAELCV>F<SFSQEIEYWGINEFFID----S--CCSYSY123
KCNS3YFDRNPSLFRYVLNFYYT-GKLHVMEELCV>F<SFCQEIEYWGINELFID----S--CCSNRY121
KCNV1FFDRSSQAFRYVLHYYRT-GRLHVMEQLCA>L<SFLQEIQYWGIDELSID----S--CCRDRY155
KCNV2FFDRDPAVFQLVYNFYLS-GVLLVLDGLCP>R<RFLEELGYWGVRLKYTP----R--CCRICF203
cons                              > <                              

See full Alignment of Paralogues


Known Variants in KCNQ1

ProteinCDSDisease ClassificationDiseasedbSNP linksEffect Prediction
p.P73Tc.217C>A Inherited ArrhythmiaLQTSSIFT: tolerated
Polyphen: benign
ReportsInherited ArrhythmiaLQTS Compendium of cardiac channel mutations in 541 consecutive unrelated patients referred for long QT syndrome genetic testing. Heart Rhythm. 2005 2(5):507-17. 15840476
Inherited ArrhythmiaLQTS Spectrum and prevalence of mutations from the first 2,500 consecutive unrelated patients referred for the FAMILION long QT syndrome genetic test. Heart Rhythm. 2009 6(9):1297-303. 19716085
Inherited ArrhythmiaLQTS Genetic testing for long-QT syndrome: distinguishing pathogenic mutations from benign variants. Circulation. 2009 120(18):1752-60. 19841300
Inherited ArrhythmiaLQTS Phylogenetic and physicochemical analyses enhance the classification of rare nonsynonymous single nucleotide variants in type 1 and 2 long-QT syndrome. Circ Cardiovasc Genet. 2012 5(5):519-28. doi: 10.1161/CIRCGENETICS.112.963785. 22949429
Unknown Novel genotype-phenotype associations demonstrated by high-throughput sequencing in patients with hypertrophic cardiomyopathy. Heart. 2015 101(4):294-301. doi: 10.1136/heartjnl-2014-306387. 25351510