TPMT

thiopurine S-methyltransferase
OMIM: 187680, Gene2Phenotype

4 panels

Panel Reviews Mode of inheritance Details
4 panels

Red TPMT in Mendeliome


Version 1.3512

1 review Unknown
Sources
  • Expert Review Red
  • Victorian Clinical Genetics Services
Phenotypes
  • {Thiopurines, poor metabolism of, 1} 610460

Green TPMT in Pharmacogenomics_Paediatric


Level 2: Screening
Version 0.50

2 reviews BIALLELIC, autosomal or pseudoautosomal
Sources
  • Expert Review Green
  • Expert list
Phenotypes
  • {Thiopurines, poor metabolism of, 1}, MIM# 610460
  • Azathioprine
  • Mercaptopurine
  • Thioguanines

Green TPMT in Transplant Co-Morbidity


Level 2: Screening
Version 0.20

1 review BOTH monoallelic and biallelic, autosomal or pseudoautosomal
Sources
  • Expert Review Green
  • Expert list
Phenotypes
  • Thiopurines, poor metabolism of, 1 MIM# 610460

Red TPMT in Nucleotide metabolism disorders


Level 2: Metabolic disorders
Version 0.8

Component of the following Super Panels:

  • Metabolic Disorders Superpanel
  • 1 review BIALLELIC, autosomal or pseudoautosomal
    Sources
    • Expert Review Red
    • Expert Review Red
    • Victorian Clinical Genetics Services
    Phenotypes
    • {Thiopurines, poor metabolism of, 1} 610460