1. Genes and Genomic Entities
  2. SLC26A5

SLC26A5

solute carrier family 26 member 5
OMIM: 604943, Gene2Phenotype

1 panel

Panel Reviews Mode of inheritance Details
1 panel
Green SLC26A5 in Monogenic hearing loss


Level 2: Audiology
Version 5.57
Latest signed off version: v5.0 (30 Apr 2025)

Component of the following Super Panels:

  • Paediatric disorders

    		•  review BIALLELIC, autosomal or pseudoautosomal
    Sources
    • Expert Review Green
    • Expert
    • Radboud University Medical Center, Nijmegen
    • Emory Genetics Laboratory
    • UKGTN
    • Illumina TruGenome Clinical Sequencing Services
    Phenotypes
    • #613865:?Deafness, autosomal recessive 61
    • Nonsyndromic Hearing Loss, Recessive
    • Deafness, autosomal recessive 61, 613865
    • hearing loss