Genomics England
GMS Panels
Panels
Genes and Entities

SLC17A8

solute carrier family 17 member 8
OMIM: 607557
PanelMode of inheritanceDetails
1 panel
Green
in Monogenic hearing loss
Component of the following Super Panels:
  • - Paediatric disorders
R-numbers: R67
Signed-off version 4.42
MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown
Phenotypes
hearing loss, Nonsyndromic Hearing Loss, Dominant, Deafness, autosomal dominant 25, 605583