Paralogue Annotation for KCNH2 residue 721

Residue details

Gene: KCNH2
Reference Sequences: LRG: LRG_288, Ensembl variant: ENST00000262186 / ENSP00000262186
Amino Acid Position: 721
Reference Amino Acid: P - Proline
Protein Domain: C-terminus


Paralogue Variants mapped to KCNH2 residue 721

No paralogue variants have been mapped to residue 721 for KCNH2.



KCNH2NPLRQRLEEYFQHAWSYTNGIDMNAVLKGF>P<ECLQADICLHLNRSLLQHCKPFRGATKGCL751
KCNH1KGLSERVMDYIVSTWSMSRGIDTEKVLQIC>P<KDMRADICVHLNRKVFKEHPAFRLASDGCL590
KCNH3KPLKQRMLEYFQATWAVNNGIDTTELLQSL>P<DELRADIAMHLHKEVL-QLPLFEAASRGCL591
KCNH4RPLKQRMLEYFQTTWAVNSGIDANELLRDF>P<DELRADIAMHLNREIL-QLPLFGAASRGCL565
KCNH5KGLSERVMDYIVSTWSMSKGIDTEKVLSIC>P<KDMRADICVHLNRKVFNEHPAFRLASDGCL559
KCNH6NPLRQRLEEYFQHAWSYTNGIDMNAVLKGF>P<ECLQADICLHLHRALLQHCPAFSGAGKGCL603
KCNH7NPLRQRLEEYFQHAWTYTNGIDMNMVLKGF>P<ECLQADICLHLNQTLLQNCKAFRGASKGCL754
KCNH8QQLKQRMLEYFQTTWSVNNGIDSNELLKDF>P<DELRSDITMHLNKEIL-QLSLFECASRGCL560
CNGA1KDMEKRVIKWFDYLWTNKKTVDEKEVLKYL>P<DKLRAEIAINVHLDTLKKVRIFADCEAGLL488
CNGA2KGMEAKVIRWFDYLWTNKKTVDEREILKNL>P<AKLRAEIAINVHLSTLKKVRIFHDCEAGLL463
CNGA3KDLETRVIRWFDYLWANKKTVDEKEVLKSL>P<DKLKAEIAINVHLDTLKKVRIFQDCEAGLL491
CNGA4RKLERRVIDWYQHLQINKKMTNEVAILQHL>P<ERLRAEVAVSVHLSTLSRVQIFQNCEASLL357
CNGB1KSVQNRVKTWYEYTWHSQGMLDESELMVQL>P<DKMRLDLAIDVNYNIVSKVALFQGCDRQMI971
CNGB3KLVQKRVRTWYEYTWDSQRMLDESDLLKTL>P<TTVQLALAIDVNFSIISKVDLFKGCDTQMI533
HCN1ADMRQKIHDYYEHRYQG-KIFDEENILNEL>N<DPLREEIVNFNCRKLVATMPLFANADPNFV484
HCN2ADFRQKIHDYYEHRYQG-KMFDEDSILGEL>N<GPLREEIVNFNCRKLVASMPLFANADPNFV553
HCN3ADTRQRIHEYYEHRYQG-KMFDEESILGEL>S<EPLREEIINFTCRGLVAHMPLFAHADPSFV437
HCN4PDTRQRIHDYYEHRYQG-KMFDEESILGEL>S<EPLREEIINFNCRKLVASMPLFANADPNFV604
cons                              > <                              

See full Alignment of Paralogues


Known Variants in KCNH2

ProteinCDSDisease ClassificationDiseasedbSNP linksEffect Prediction
p.P721Lc.2162C>T Inherited ArrhythmiaLQTSSIFT: deleterious
Polyphen: probably damaging
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 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
Inherited ArrhythmiaLQTS Large-scale mutational analysis of Kv11.1 reveals molecular insights into type 2 long QT syndrome. Nat Commun. 2014 5:5535. doi: 10.1038/ncomms6535. 25417810
p.P721Rc.2162C>G Inherited ArrhythmiaLQTSSIFT:
Polyphen:
ReportsInherited ArrhythmiaLQTS Asymmetry of parental origin in long QT syndrome: preferential maternal transmission of KCNQ1 variants linked to channel dysfunction. Eur J Hum Genet. 2016 24(8):1160-6. doi: 10.1038/ejhg.2015.257. 26669661