MT-TW

mitochondrially encoded tRNA tryptophan
OMIM: 590095, Gene2Phenotype

5 panels

Panel Reviews Mode of inheritance Details
5 panels

Green MT-TW in Undiagnosed metabolic disorders

Level 3: Specific metabolic abnormalities
Level 2: Metabolic disorders
Version 1.542

review MITOCHONDRIAL
Sources
  • Expert Review Green
Tags
  • gene-checked

Green MT-TW in Inborn errors of metabolism


Version 2.263
Latest signed off version: v2.3 (17 Feb 2020)

Component of the following Super Panels:

  • Hypotonic infant
  • Paediatric disorders
  • White matter disorders - childhood onset
  • review MITOCHONDRIAL
    Sources
    • Expert Review Green
    Tags
    • gene-checked

    Green MT-TW in Mitochondrial disorders

    Level 3: Mitochondrial
    Level 2: Metabolic disorders
    Version 2.117
    Latest signed off version: v2.4 (17 Feb 2020)

    Component of the following Super Panels:

  • White matter disorders - childhood onset
  • review MITOCHONDRIAL
    Sources
    • Expert Review Green
    • UKGTN
    Tags
    • gene-checked

    No list MT-TW in Childhood onset dystonia or chorea or related movement disorder


    Version 1.246
    Latest signed off version: v1.137 (5 Aug 2021)

    review MITOCHONDRIAL
    Sources
    • Expert Review Removed
    • London North GLH
    Tags
    • curated_removed

    Green MT-TW in Severe Paediatric Disorders


    Version 1.127

    review MITOCHONDRIAL
    Sources
    • Next Generation Children Project
    • Expert Review Green
    • Expert list
    Phenotypes
    • MYOPATHY, MITOCHONDRIAL
    • ENCEPHALOPATHY, MITOCHONDRIAL
    • NEUROGASTROINTESTINAL SYNDROME, MITOCHONDRIAL
    • ENCEPHALOCARDIOMYOPATHY, MITOCHONDRIAL
    • ENCEPHALOMYOPATHY, MITOCHONDRIAL