Mine Disruption Phenotype

Gene Info

  • Species: Mouse (Mus musculus)
  • GeneID: 17772
  • Symbol: Mtm1
  • Description: X-linked myotubular myopathy gene 1
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Gene ID Entry Entry Name Protein Name Type Information
17772 Q9Z2C5 MTM1_MOUSE Myotubularin (Phosphatidylinositol-3,5-bisphosphate 3-phosphatase) (EC 3.1.3.95) (Phosphatidylinositol-3-phosphate phosphatase) (EC 3.1.3.64) DISRUPTION PHENOTYPE Mice are viable although lifespan is severely reduced. An under-representation of mutant males suggests some prenatal lethality. Generalized and progressive myopathy starts at around 4 weeks of age with amyotrophy and accumulation of central nuclei in skeletal muscle fibers, leading to death at 6-14 weeks. Mutants also show mitochondrial disorganization and increased levels of desmin with abnormal desmin intermediate filament formation and architecture. {ECO:0000269|PubMed:12391329, ECO:0000269|PubMed:21135508}.