CLCNKB - Gene browser

CLCNKB

chloride voltage-gated channel Kb

HCNC Approved Symbol: CLCNKB (HGNC:2027)
Genomic Coordinates: 1:16,043,782 - 16,057,326 (1p36.13)
Synonyms: hClC-Kb, CLCKB, ClC-K2, ClC-Kb
Disease Associations: This gene is associated with the following 2 diseases in OMIM.

Diagnosed Cases

9Patients

In total, 9 patients were diagnosed with a variant in the CLCNKB gene.

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

09
Patient count

Hypokalemia: 4 (44.4%)
Patient Count: 4 (44.4%)
% of total patients presenting each phenotype is shown in parentheses.
4 (44.4%)
Hyperkaliuresis: 2 (22.2%)
Patient Count: 2 (22.2%)
% of total patients presenting each phenotype is shown in parentheses.
2 (22.2%)
Hypokalemic alkalosis: 2 (22.2%)
Patient Count: 2 (22.2%)
% of total patients presenting each phenotype is shown in parentheses.
2 (22.2%)
Hypomagnesemia: 2 (22.2%)
Patient Count: 2 (22.2%)
% of total patients presenting each phenotype is shown in parentheses.
2 (22.2%)
Cystic kidney disease: 2 (22.2%)
Patient Count: 2 (22.2%)
% of total patients presenting each phenotype is shown in parentheses.
2 (22.2%)