Paralogue Annotation for KCNJ2 residue 227

Residue details

Gene: KCNJ2
Reference Sequences: LRG: LRG_328, Ensembl variant: ENST00000535240 / ENSP00000441848
Amino Acid Position: 227
Reference Amino Acid: V - Valine
Protein Domain: C-terminus


Paralogue Variants mapped to KCNJ2 residue 227

No paralogue variants have been mapped to residue 227 for KCNJ2.



KCNJ2HNAVIAMRDGKLCLMWRVGNLRKSHLVEAH>V<RAQLLKSRITSEGEYIPLDQIDINVGFD--255
KCNJ1KNAVISKRGGKLCLLIRVANLRKSLLIGSH>I<YGKLLKTTVTPEGETIILDQININFVVD--254
KCNJ3EHAVISMRDGKLTLMFRVGNLRNSHMVSAQ>I<RCKLLKSRQTPEGEFLPLDQLELDVGFS--256
KCNJ4HHAVISVRDGKLCLMWRVGNLRKSHIVEAH>V<RAQLIKPYMTQEGEYLPLDQRDLNVGYD--247
KCNJ5NNAVISMRDEKLCLMFRVGDLRNSHIVEAS>I<RAKLIKSRQTKEGEFIPLNQTDINVGFD--262
KCNJ6THAVISMRDGKLCLMFRVGDLRNSHIVEAS>I<RAKLIKSKQTSEGEFIPLNQTDINVGYY--265
KCNJ8RHAVIAVRNGKLCFMFRVGDLRKSMIISAS>V<RIQVVKKTTTPEGEVVPIHQLDIPVDNP--253
KCNJ9SHAVVSLRDGRLCLMFRVGDLRSSHIVEAS>I<RAKLIRSRQTLEGEFIPLHQTDLSVGFD--233
KCNJ10QHAVVASHNGKPCLMIRVANMRKSLLIGCQ>V<TGKLLQTHQTKEGENIRLNQVNVTFQVD--241
KCNJ11KHAVIALRHGRLCFMLRVGDLRKSMIISAT>I<HMQVVRKTTSPEGEVVPLHQVDIPMENG--243
KCNJ12HNAVVALRDGKLCLMWRVGNLRKSHIVEAH>V<RAQLIKPRVTEEGEYIPLDQIDIDVGFD--256
KCNJ13DTAVVAHMDGKPNLIFQVANTRPSPLTSVR>V<SAVLYQERENGK----L-YQTSVDFHLDGI229
KCNJ14ENAVVALRDHRLCLMWRVGNLRRSHLVEAH>V<RAQLLQPRVTPEGEYIPLDHQDVDVGFD--260
KCNJ15HCAVITKQNGKLCLVIQVANMRKSLLIQCQ>L<SGKLLQTHVTKEGERILLNQATVKFHVD--240
KCNJ16YFALIGMRDGKLCLMWRIGDFRPNHVVEGT>V<RAQLLRYTEDSEGRM-TMAFKDLKLV----241
cons                              > <                              

See full Alignment of Paralogues


Known Variants in KCNJ2

ProteinCDSDisease ClassificationDiseasedbSNP linksEffect Prediction
p.V227Fc.679G>T Other Cardiac PhenotypeSIFT: deleterious
Polyphen: probably damaging
ReportsOther Cardiac Phenotype Genotypic heterogeneity and phenotypic mimicry among unrelated patients referred for catecholaminergic polymorphic ventricular tachycardia genetic testing. Heart Rhythm. 2006 3(7):800-5. 16818210
Other Cardiac Phenotype Protein kinase A-dependent biophysical phenotype for V227F-KCNJ2 mutation in catecholaminergic polymorphic ventricular tachycardia. Circ Arrhythm Electrophysiol. 2009 2(5):540-7. 19843922
Other Cardiac Phenotype New exome data question the pathogenicity of genetic variants previously associated with catecholaminergic polymorphic ventricular tachycardia. Circ Cardiovasc Genet. 2013 6(5):481-9. doi: 10.1161/CIRCGENETICS.113.000118. 24025405