PanelApp (staging)
  1. Genes and Genomic Entities
  2. GNMT

GNMT

glycine N-methyltransferase
OMIM: 606628, ClinGen, DECIPHER

3 panels

Panel Reviews Mode of inheritance Details
3 panels

Green GNMT in Mendeliome


Version 1.2302

1 review BIALLELIC, autosomal or pseudoautosomal
Sources
  • Expert Review Green
  • NHS GMS
  • Victorian Clinical Genetics Services
Phenotypes
  • Glycine N-methyltransferase deficiency MIM#606664
  • Disorders of the metabolism of sulphur amino acids

Green GNMT in Miscellaneous Metabolic Disorders


Level 2: Metabolic disorders
Version 1.48

Component of the following Super Panels:

  • Metabolic Disorders Superpanel
  • Progressive Neurological Conditions

    		•  1 review BIALLELIC, autosomal or pseudoautosomal
    Sources
    • Expert Review Green
    • NHS GMS
    Phenotypes
    • Glycine N-methyltransferase deficiency MIM#606664
    • Disorders of the metabolism of sulphur amino acids

    Red GNMT in Aminoacidopathy


    Level 2: Metabolic disorders
    Version 1.133

    Component of the following Super Panels:

  • Metabolic Disorders Superpanel

    		•  1 review BIALLELIC, autosomal or pseudoautosomal
    Sources
    • Expert Review Red
    • ClinGen
    Phenotypes
    • glycine N-methyltransferase deficiency MONDO:0011698