Genomics England
GMS Panels
Panels
Genes and Entities

MT-TF

mitochondrially encoded tRNA phenylalanine
OMIM: 590070
PanelMode of inheritanceDetails
4 panels
Green
in Likely inborn error of metabolism - targeted testing not possible
Component of the following Super Panels:
  • - Childhood onset leukodystrophy
  • - Hypotonic infant
  • - Paediatric disorders
  • - Unexplained death in infancy and sudden unexplained death in childhood
R-numbers: R98
Signed-off version 4.0
MITOCHONDRIAL
Phenotypes
Green
in Mitochondrial disorders
Component of the following Super Panels:
  • - Childhood onset leukodystrophy
Signed-off version 4.0
MITOCHONDRIAL
Phenotypes
Green
in Tubulointerstitial kidney disease
R-numbers: R202
Signed-off version 3.0
MITOCHONDRIAL
Phenotypes
Tubulointerstitial kidney disease, tubulointerstitial nephritis, renal insufficiency, renal failure
Green
in Unexplained young onset end-stage renal disease
R-numbers: R257
Signed-off version 3.0
MITOCHONDRIAL
Phenotypes
renal insufficiency, Tubulointerstitial kidney disease, tubulointerstitial nephritis, renal failur