Mine Disruption Phenotype

Gene Info

  • Species: Mouse (Mus musculus)
  • GeneID: 20190
  • Symbol: Ryr1
  • Description: ryanodine receptor 1, skeletal muscle
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Gene ID Entry Entry Name Protein Name Type Information
20190 E9PZQ0 RYR1_MOUSE Ryanodine receptor 1 (RYR-1) (RyR1) (Skeletal muscle calcium release channel) (Skeletal muscle ryanodine receptor) (Skeletal muscle-type ryanodine receptor) (Type 1 ryanodine receptor) DISRUPTION PHENOTYPE Perinatal lethality, due to severe defects in skeletal muscle development. Neonates do not breathe and do not move. Mutant mice show defects in muscle fiber development. Their muscles do not show a contractile response to electrical stimulation. In addition, mice display abnormal curvature of the spine, thin limbs, and an abnormal rib cage. {ECO:0000269|PubMed:7515481}.