CLDN14 - Gene browser | 3billion

CLDN14

CLDN14

claudin 14

HCNC Approved Symbol: CLDN14 (HGNC:2035)
Genomic Coordinates: 21:36,460,621 - 36,576,569 (21q22.13)
Synonyms: DFNB29
Disease Associations: This gene is associated with the following 1 diseases in OMIM.

Diagnosed Cases

3Patients

In total, 3 patients were diagnosed with a variant in the CLDN14 gene.

Frequently observed phenotypes(Top 5 only)

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

03
Patient count

Hearing loss: 1 (33.3%)
Patient Count: 1 (33.3%)
% of total patients presenting each phenotype is shown in parentheses.
1 (33.3%)

Last updated: 2024-06-30

CLDN14 - Gene browser | 3billion