KCNQ5 - Gene browser | 3billion

KCNQ5

KCNQ5

potassium voltage-gated channel subfamily Q member 5

HCNC Approved Symbol: KCNQ5 (HGNC:6299)
Genomic Coordinates: 6:72,622,064 - 73,198,853 (6q13)
Synonyms: Kv7.5
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 KCNQ5 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

Global developmental delay: 1 (50.0%)
Patient Count: 1 (50.0%)
% of total patients presenting each phenotype is shown in parentheses.
1 (50.0%)
Seizure: 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

KCNQ5 - Gene browser | 3billion