KCNQ4 - Gene browser | 3billion

KCNQ4

KCNQ4

potassium voltage-gated channel subfamily Q member 4

HCNC Approved Symbol: KCNQ4 (HGNC:6298)
Genomic Coordinates: 1:40,783,787 - 40,840,452 (1p34.2)
Synonyms: Kv7.4, DFNA2
Disease Associations: This gene is associated with the following 1 diseases in OMIM.

Diagnosed Cases

11Patients

In total, 11 patients were diagnosed with a variant in the KCNQ4 gene.

Frequently observed phenotypes(Top 5 only)

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

011
Patient count

Hearing loss: 5 (45.5%)
Patient Count: 5 (45.5%)
% of total patients presenting each phenotype is shown in parentheses.
5 (45.5%)
Bilateral progressive sensorineural hearing loss: 1 (9.1%)
Patient Count: 1 (9.1%)
% of total patients presenting each phenotype is shown in parentheses.
1 (9.1%)
Hearing impairment: 1 (9.1%)
Patient Count: 1 (9.1%)
% of total patients presenting each phenotype is shown in parentheses.
1 (9.1%)

Last updated: 2024-06-30

KCNQ4 - Gene browser | 3billion