1. Genes and Genomic Entities
  2. SLC17A8

SLC17A8

solute carrier family 17 member 8
OMIM: 607557, Gene2Phenotype

1 panel

Panel Reviews Mode of inheritance Details
1 panel
Green SLC17A8 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 MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown
    Sources
    • Expert Review Green
    • Expert
    • Radboud University Medical Center, Nijmegen
    • Emory Genetics Laboratory
    • UKGTN
    • Illumina TruGenome Clinical Sequencing Services
    Phenotypes
    • hearing loss
    • Nonsyndromic Hearing Loss, Dominant
    • Deafness, autosomal dominant 25, 605583