1. Genes and Genomic Entities
  2. SLC26A6

SLC26A6

solute carrier family 26 member 6
OMIM: 610068, Gene2Phenotype

2 panels

Panel Reviews Mode of inheritance Details
2 panels
Red SLC26A6 in Nephrocalcinosis or nephrolithiasis

Level 3: Disorders of function
Level 2: Renal and urinary tract disorders
Version 4.13
Latest signed off version: v4.0 (22 Mar 2023)

Component of the following Super Panels:

  • Renal superpanel - broad
  • Renal superpanel - narrow

    		•  review MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown
    Sources
    • Literature
    Phenotypes
    • Enteric hyperoxaluria and nephrolithiasis
    Tags
    • watchlist
    Red SLC26A6 in Likely inborn error of metabolism - targeted testing not possible


    Version 5.1
    Latest signed off version: v5.0 (1 May 2024)

    Component of the following Super Panels:

  • Childhood onset leukodystrophy
  • Hypotonic infant
  • Paediatric disorders
  • Unexplained death in infancy and sudden unexplained death in childhood

    		•  review MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown
    Sources
    • Literature
    Phenotypes
    • Enteric hyperoxaluria and nephrolithiasis
    Tags
    • watchlist