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 2: Renal
Version 6.1
Latest signed off version: v6.0 (6 May 2026)

Component of the following Super Panels:

  • Unexplained young onset end-stage renal disease

    		•  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


    Level 2: Metabolic
    Version 9.4
    Latest signed off version: v9.0 (6 May 2026)

    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