KCNQ1 - Gene browser

KCNQ1

potassium voltage-gated channel subfamily Q member 1

HCNC Approved Symbol: KCNQ1 (HGNC:6294)
Genomic Coordinates: 11:2,445,008 - 2,849,105 (11p15.5-p15.4)
Synonyms: Kv7.1, KCNA8, KVLQT1, JLNS1, LQT1, LQT, KCNA9
Disease Associations: This gene is associated with the following 5 diseases in OMIM.

Diagnosed Cases

35Patients

In total, 35 patients were diagnosed with a variant in the KCNQ1 gene.

(Top 5 only, Patient count*)
*% of total patients presenting each phenotype is shown in parentheses.

035
Patient count

Left ventricular hypertrophy: 5 (14.3%)
Patient Count: 5 (14.3%)
% of total patients presenting each phenotype is shown in parentheses.
5 (14.3%)
Prolonged qt interval: 5 (14.3%)
Patient Count: 5 (14.3%)
% of total patients presenting each phenotype is shown in parentheses.
5 (14.3%)
Syncope: 5 (14.3%)
Patient Count: 5 (14.3%)
% of total patients presenting each phenotype is shown in parentheses.
5 (14.3%)
Intellectual disability: 3 (8.6%)
Patient Count: 3 (8.6%)
% of total patients presenting each phenotype is shown in parentheses.
3 (8.6%)
Arrhythmias: 3 (8.6%)
Patient Count: 3 (8.6%)
% of total patients presenting each phenotype is shown in parentheses.
3 (8.6%)