1. Genes and Genomic Entities
  2. CLDN14

CLDN14

claudin 14
OMIM: 605608, Gene2Phenotype

2 panels

Panel Reviews Mode of inheritance Details
2 panels
Green CLDN14 in Monogenic hearing loss

Level 3: Non-syndromic hearing loss
Level 2: Hearing and ear disorders
Version 4.36
Latest signed off version: v4.0 (22 Mar 2023)

Component of the following Super Panels:

  • Paediatric disorders

    		•  review BIALLELIC, autosomal or pseudoautosomal
    Sources
    • Expert Review Green
    • Expert
    • Illumina TruGenome Clinical Sequencing Services
    • Emory Genetics Laboratory
    • Radboud University Medical Center, Nijmegen
    • UKGTN
    Phenotypes
    • hearing loss
    • Nonsyndromic Hearing Loss, Recessive
    • #614035:Deafness, autosomal recessive 29
    Green CLDN14 in Severe Paediatric Disorders


    Version 1.184

    		review BIALLELIC, autosomal or pseudoautosomal
    Sources
    • Next Generation Children Project
    • Expert Review Green
    • Expert list
    Phenotypes
    • Deafness, autosomal recessive 29, 614035