TNPO3

transportin 3
OMIM: 610032, Gene2Phenotype

1 panel

Panel Reviews Mode of inheritance Details
1 panel
Green TNPO3 in Limb girdle muscular dystrophies, myofibrillar myopathies and distal myopathies

Level 3: Neuromuscular disorders
Level 2: Neurology and neurodevelopmental disorders
Version 4.32
Latest signed off version: v4.0 (22 Mar 2023)

Component of the following Super Panels:

  • Hypotonic infant
  • Other rare neuromuscular disorders
  • review MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown
    Sources
    • Expert Review Green
    • Yorkshire and North East GLH
    • NHS GMS
    • Expert Review
    Phenotypes
    • Muscular dystrophy, limb-girdle, autosomal dominant 2, 608423