POU4F3 - Gene browser

POU4F3

POU class 4 homeobox 3

HCNC Approved Symbol: POU4F3 (HGNC:9220)
Genomic Coordinates: 5:146,338,839 - 146,341,728 (5q32)
Synonyms: BRN3C, DFNA15, DFNA52, DFNA42
Disease Associations: This gene is associated with the following 1 diseases in OMIM.

17Patients

In total, 17 patients were diagnosed with a variant in the POU4F3 gene.

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

017
Patient count

Hearing loss: 11 (64.7%)
Patient Count: 11 (64.7%)
% of total patients presenting each phenotype is shown in parentheses.
11 (64.7%)
Dizziness: 2 (11.8%)
Patient Count: 2 (11.8%)
% of total patients presenting each phenotype is shown in parentheses.
2 (11.8%)
Hearing abnormality: 1 (5.9%)
Patient Count: 1 (5.9%)
% of total patients presenting each phenotype is shown in parentheses.
1 (5.9%)
Hearing loss, sensorineural: 1 (5.9%)
Patient Count: 1 (5.9%)
% of total patients presenting each phenotype is shown in parentheses.
1 (5.9%)
Progressive hearing impairment: 1 (5.9%)
Patient Count: 1 (5.9%)
% of total patients presenting each phenotype is shown in parentheses.
1 (5.9%)