Paralogue Annotation for KCNQ1 residue 51

Residue details

Gene: KCNQ1
Reference Sequences: LRG: LRG_287, Ensembl variant: ENST00000155840 / ENSP00000155840
Amino Acid Position: 51
Reference Amino Acid: Y - Tyrosine
Protein Domain: N-terminus


Paralogue Variants mapped to KCNQ1 residue 51

No paralogue variants have been mapped to residue 51 for KCNQ1.



KCNQ1-P---------------------A--GGAL>Y<APIAPGAPGP--------APPASPAAPAAP73
KCNQ2-E---------------------------->-<----A-PK---------------RGSILS-55
KCNQ3-R---------------------------->-<--------DEG-----QR---R----TPQ-83
KCNQ4-P---------------------------->-<--RRLGLLGSP-----L------PPGAPLP59
KCNQ5-A---------------------------->-<--ATLGGGGGG-----LRESRRGKQGARMS88
KCNA1-------------KR-M---RYFDPLRNEY>F<FDRNRPSFDAILYYYQSGGRLRRPVNVPLD111
KCNA10-------------KR-M---QFFDSMRNEY>F<FDRNRPSFDGILYYYQSGGKIRRPANVPID160
KCNA2-------------KR-M---RYFDPLRNEY>F<FDRNRPSFDAILYYYQSGGRLRRPVNVPLD107
KCNA3-------------RR-M---RYFDPLRNEY>F<FDRNRPSFDAILYYYQSGGRIRRPVNVPID178
KCNA4-------------KR-T---QYFDPLRNEY>F<FDRNRPSFDAILYYYQSGGRLKRPVNVPFD250
KCNA5-------------KR-L---RYFDPLRNEY>F<FDRNRPSFDGILYYYQSGGRLRRPVNVSLD194
KCNA6-------------RR-V---RFFDPLRNEY>F<FDRNRPSFDAILYYYQSGGRLRRPVNVPLD115
KCNA7-------------RR-G---RFYDDARREY>F<FDRHRPSFDAVLYYYQSGGRLRRPAHVPLD87
KCNB1-HD----------SL-LEVCDDYSLDDNEY>F<FDRHPGAFTSILNFYRT-GRLHMMEEMCAL113
KCNB2-HE----------SL-LEVCDDYNLNENEY>F<FDRHPGAFTSILNFYRT-GKLHMMEEMCAL117
KCNC1----------------S--HFDYDPRADEF>F<FDRHPGVFAHILNYYRT-GKLHCPADVCGP85
KCNC2-------------RGGR--ASDHPGGGREF>F<FDRHPGVFAYVLNYYRT-GKLHCPADVCGP132
KCNC3----------------A--RFDYDPGADEF>F<FDRHPGVFAYVLNYYRT-GKLHCPADVCGP165
KCNC4---------------GS--SGSSGGGGCEF>F<FDRHPGVFAYVLNYYRT-GKLHCPADVCGP124
KCND1-------------KE-F----FYDADSGEY>F<FDRDPDMFRHVLNFYRT-GRLHCPRQECIQ112
KCND2-------------RD-F----FYHPETQQY>F<FDRDPDIFRHILNFYRT-GKLHYPRHECIS113
KCND3-------------KE-F----FFNEDTKEY>F<FDRDPEVFRCVLNFYRT-GKLHYPRYECIS112
KCNF1GYD----------TI-FSLCDDYDPGKREF>Y<FDRDPDAFKCVIEVYYF-GEVHMKKGICPI107
KCNG1-FD----------DI-LNVCDDYDVTCNEF>F<FDRNPGAFGTILTFLRA-GKLRLLREMCAL145
KCNG2-HD----------DL-LRVCDDYDVSRDEF>F<FDRSPCAFRAIVALLRA-GKLRLLRGPCAL99
KCNG3-ER----------DV-LEVCDDYDRERNEY>F<FDRHSEAFGFILLYVRGHGKLRFAPRMCEL92
KCNG4-YE----------EI-VQLCDDYDEDSQEF>F<FDRSPSAFGVIVSFLAA-GKLVLLQEMCAL141
KCNS1-EE----------QA-RRLCDDYDEAAREF>Y<FDRHPGFFLSLLHFYRT-GHLHVLDELCVF132
KCNS2-RE----------AI-LELCDDYDDVQREF>Y<FDRNPELFPYVLHFYHT-GKLHVMAELCVF99
KCNS3-EE----------AI-LELCDDYSVADKEY>Y<FDRNPSLFRYVLNFYYT-GKLHVMEELCVF97
KCNV1-SYRRPGALAAVPSP-LELCDDANPVDNEY>F<FDRSSQAFRYVLHYYRT-GRLHVMEQLCAL131
KCNV2-RS----------RQ-LSLCDDYEEQTDEY>F<FDRDPAVFQLVYNFYLS-GVLLVLDGLCPR179
cons                              > <                              

See full Alignment of Paralogues


Known Variants in KCNQ1

ProteinCDSDisease ClassificationDiseasedbSNP linksEffect Prediction
p.Y51Cc.152A>G Other Cardiac PhenotypeSIFT:
Polyphen:
ReportsOther Cardiac Phenotype Cardiac channelopathy testing in 274 ethnically diverse sudden unexplained deaths. Forensic Sci Int. 2014 237:90-9. doi: 10.1016/j.forsciint.2014.01.014. 24631775