ClinGen Dosage Sensitivity Curation Page

CLDN14

  • Curation Status: Complete

Location Information

Select assembly: (NC_000021.8) (NC_000021.9)

Haploinsufficiency phenotype comments:

Variation in CLDN14 has been reported in individuals with autosomal recessive nonsyndromic deafness characterized by severe to profound prelingual onset. Furthermore, the overall evidence that CLDN14, when altered via biallelic loss of function, causes autosomal recessive nonsyndromic deafness was assessed by the ClinGen Hearing Loss Working Group and classified as DEFINITIVE after primary curation.

  • Triplosensitivity score: 0
  • Strength of Evidence (disclaimer): No evidence for dosage pathogenicity