×
Entrez Id:
3784
Gene Symbol:
KCNQ1
KCNQ1
1.000
GeneticVariation
disease
UNIPROT
KCNQ1 and KCNH2 mutations associated with long QT syndrome in a Chinese population.
12442276
2002
×
Entrez Id:
3784
Gene Symbol:
KCNQ1
KCNQ1
1.000
GeneticVariation
disease
UNIPROT
Compendium of cardiac channel mutations in 541 consecutive unrelated patients referred for long QT syndrome genetic testing.
15840476
2005
×
Entrez Id:
3784
Gene Symbol:
KCNQ1
KCNQ1
1.000
GeneticVariation
disease
UNIPROT
Genetic testing in the long QT syndrome: development and validation of an efficient approach to genotyping in clinical practice.
16414944
2005
×
Entrez Id:
3784
Gene Symbol:
KCNQ1
KCNQ1
1.000
GeneticVariation
disease
UNIPROT
Spectrum of pathogenic mutations and associated polymorphisms in a cohort of 44 unrelated patients with long QT syndrome.
16922724
2006
×
Entrez Id:
3784
Gene Symbol:
KCNQ1
KCNQ1
1.000
GeneticVariation
disease
UNIPROT
The KCNQ1 (Kv7.1) COOH terminus, a multitiered scaffold for subunit assembly and protein interaction.
18165683
2008
×
Entrez Id:
3784
Gene Symbol:
KCNQ1
KCNQ1
1.000
GeneticVariation
disease
UNIPROT
Identification of a novel KCNQ1 mutation associated with both Jervell and Lange-Nielsen and Romano-Ward forms of long QT syndrome in a Chinese family.
18400097
2008
×
Entrez Id:
3784
Gene Symbol:
KCNQ1
KCNQ1
1.000
GeneticVariation
disease
UNIPROT
Biophysical characterization of KCNQ1 P320 mutations linked to long QT syndrome 1 .
19540844
2010
×
Entrez Id:
3784
Gene Symbol:
KCNQ1
KCNQ1
1.000
GeneticVariation
disease
UNIPROT
Spectrum and prevalence of mutations from the first 2,500 consecutive unrelated patients referred for the FAMILION long QT syndrome genetic test.
19716085
2009
×
Entrez Id:
3784
Gene Symbol:
KCNQ1
KCNQ1
1.000
GeneticVariation
disease
UNIPROT
Biophysical properties of 9 KCNQ1 mutations associated with long-QT syndrome.
19808498
2009
×
Entrez Id:
3784
Gene Symbol:
KCNQ1
KCNQ1
1.000
GeneticVariation
disease
UNIPROT
Biophysical properties of mutant KCNQ1 S277L channels linked to hereditary long QT syndrome with phenotypic variability.
21241800
2011
×
Entrez Id:
3784
Gene Symbol:
KCNQ1
KCNQ1
1.000
GeneticVariation
disease
UNIPROT
A molecular mechanism for adrenergic-induced long QT syndrome.
24184248
2014
×
Entrez Id:
3784
Gene Symbol:
KCNQ1
KCNQ1
1.000
GeneticVariation
disease
UNIPROT
We identified a multigenerational LQT1 family whereby 79% of the patients genotype-positive for p.Ile235Asn-KCNQ1 (I235N-Kv7.1) have concealed LQT1 .
24269949
2014
×
Entrez Id:
3784
Gene Symbol:
KCNQ1
KCNQ1
1.000
GeneticVariation
disease
UNIPROT
A590T mutation in KCNQ1 C-terminal helix D decreases IKs channel trafficking and function but not Yotiao interaction.
24713462
2014
×
Entrez Id:
3784
Gene Symbol:
KCNQ1
KCNQ1
1.000
GeneticVariation
disease
UNIPROT
Long QT mutations at the interface between KCNQ1 helix C and KCNE1 disrupt I(KS) regulation by PKA and PIP₂.
25037568
2014
×
Entrez Id:
3784
Gene Symbol:
KCNQ1
KCNQ1
1.000
GeneticVariation
disease
UNIPROT
Mutations in KCNQ1 , encoding for Kv7.1, the α-subunit of the IKs channel, cause long-QT syndrome type 1 , potentially predisposing patients to ventricular tachyarrhythmias and sudden cardiac death, in particular, during elevated sympathetic tone.
25139741
2014
×
Entrez Id:
3784
Gene Symbol:
KCNQ1
KCNQ1
1.000
GeneticVariation
disease
UNIPROT
Cellular mechanisms of mutations in Kv7.1: auditory functions in Jervell and Lange-Nielsen syndrome vs. Romano-Ward syndrome.
25705178
2015