SLC6A20

solute carrier family 6 member 20
OMIM: 605616, Gene2Phenotype

3 panels

Panel Reviews Mode of inheritance Details
3 panels

Red SLC6A20 in Mendeliome


Version 1.1902

review MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
Sources
  • Expert Review Red
  • Victorian Clinical Genetics Services
Phenotypes
  • Hyperglycinuria, MIM# 138500

Red SLC6A20 in Aminoacidopathy


Level 2: Metabolic disorders
Version 1.128

Component of the following Super Panels:

  • Metabolic Disorders Superpanel
  • review MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
    Sources
    • Expert Review Red
    • Other
    Phenotypes
    • Hyperglycinuria MONDO:0007677

    Red SLC6A20 in Renal Tubulopathies and related disorders


    Level 2: Renal and urinary tract disorders
    Version 1.14

    Component of the following Super Panels:

  • Kidneyome_SuperPanel
  • review MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
    Sources
    • Expert Review Red
    • Expert list
    • Expert list
    Phenotypes
    • Hyperglycinuria, MIM# 138500