KCNC2 - Gene browser | 3billion

KCNC2

KCNC2

potassium voltage-gated channel subfamily C member 2

HCNC Approved Symbol: KCNC2 (HGNC:6234)
Genomic Coordinates: 12:75,040,078 - 75,209,839 (12q21.1)
Synonyms: Kv3.2
Disease Associations: This gene is associated with the following 1 diseases in OMIM.

Diagnosed Cases

2Patients

In total, 2 patients were diagnosed with a variant in the KCNC2 gene.

Frequently observed phenotypes(Top 5 only)

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

02
Patient count

Delayed development: 1 (50.0%)
Patient Count: 1 (50.0%)
% of total patients presenting each phenotype is shown in parentheses.
1 (50.0%)
Epilepsy: 1 (50.0%)
Patient Count: 1 (50.0%)
% of total patients presenting each phenotype is shown in parentheses.
1 (50.0%)
Generalized seizures: 1 (50.0%)
Patient Count: 1 (50.0%)
% of total patients presenting each phenotype is shown in parentheses.
1 (50.0%)

Last updated: 2024-06-30

KCNC2 - Gene browser | 3billion