MT-TF

mitochondrially encoded tRNA phenylalanine
OMIM: 590070, Gene2Phenotype

7 panels

Panel Reviews Mode of inheritance Details
7 panels
Green MT-TF in Tubulointerstitial kidney disease


Version 3.3
Latest signed off version: v3.0 (22 Mar 2023)

Component of the following Super Panels:

  • Renal superpanel - broad
  • Renal superpanel - narrow
  • review MITOCHONDRIAL
    Sources
    • Expert Review Green
    • Literature
    Phenotypes
    • Tubulointerstitial kidney disease
    • tubulointerstitial nephritis
    • renal insufficiency
    • renal failure
    Tags
    • gene-checked
    Green MT-TF in Unexplained young onset end-stage renal disease


    Version 3.42
    Latest signed off version: v3.0 (22 Mar 2023)

    Component of the following Super Panels:

  • Renal superpanel - broad
  • review MITOCHONDRIAL
    Sources
    • Expert Review Green
    • NHS GMS
    Phenotypes
    • renal insufficiency
    • Tubulointerstitial kidney disease
    • tubulointerstitial nephritis
    • renal failur
    Tags
    • gene-checked
    Green MT-TF in Undiagnosed metabolic disorders

    Level 3: Specific metabolic abnormalities
    Level 2: Metabolic disorders
    Version 1.617

    review MITOCHONDRIAL
    Sources
    • Expert Review Green
    Tags
    • gene-checked
    Green MT-TF in Likely inborn error of metabolism - targeted testing not possible


    Version 4.137
    Latest signed off version: v4.0 (22 Mar 2023)

    Component of the following Super Panels:

  • Childhood onset leukodystrophy
  • Hypotonic infant
  • Paediatric disorders
  • Unexplained death in infancy and sudden unexplained death in childhood
  • review MITOCHONDRIAL
    Sources
    • Expert Review Green
    Tags
    • gene-checked
    Green MT-TF in Mitochondrial disorders

    Level 3: Mitochondrial
    Level 2: Metabolic disorders
    Version 4.169
    Latest signed off version: v4.0 (22 Mar 2023)

    Component of the following Super Panels:

  • Childhood onset leukodystrophy
  • review MITOCHONDRIAL
    Sources
    • Expert Review Green
    • UKGTN
    Tags
    • gene-checked
    No list MT-TF in Childhood onset dystonia, chorea or related movement disorder


    Version 3.78
    Latest signed off version: v3.0 (22 Mar 2023)

    review MITOCHONDRIAL
    Sources
    • Expert Review Removed
    • London North GLH
    Tags
    • curated_removed
    Green MT-TF in Severe Paediatric Disorders


    Version 1.184

    review MITOCHONDRIAL
    Sources
    • Next Generation Children Project
    • Expert Review Green
    • Expert list
    Phenotypes
    • MYOPATHY, MITOCHONDRIAL, LATE-ONSET
    • EPILEPSY, MITOCHONDRIAL
    • NEPHROPATHY, TUBULOINTERSTITIAL
    • ENCEPHALOPATHY, MITOCHONDRIAL
    • MELAS SYNDROME
    • MERRF SYNDROME