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Phenotypes Associated with This Genotype
Genotype
MGI:3783340
Allelic
Composition
Rettm2.1Heno/Rettm2.1Heno
Genetic
Background
involves: C57BL/6 * FVB/N * SJL
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Rettm2.1Heno mutation (0 available); any Ret mutation (52 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
nervous system
• reduced fusimotor innervation of muscle spindles
• muscle spindle innervation normal in Rectus femoris
• peroneal muscles totally lack both motor and sensory innervation in 42% of homozygotes
• 58% with normal peroneal innervation or with innervation absent only in the superficial peroneal muscles
• posterior Psoas major lacks innervation
• variable lack of innervation of Gluteus maximus, Tensor fascia latae, and Iliopsoas
• loss of more than 20% of motor neurons at the lumbar level
• elevated apoptosis of motor neurons between 13.5 and E15.5

muscle
• reduced in size but with normal motor innervation
• reduced fusimotor innervation of muscle spindles
• muscle spindle innervation normal in Rectus femoris
• muscles lacking moter innervation display gross atrophy (peroneal, psoas major, tensor facia latae, etc)

limbs/digits/tail
• reduced in size but with normal motor innervation


Contributing Projects:
Mouse Genome Database (MGD), Gene Expression Database (GXD), Mouse Models of Human Cancer database (MMHCdb) (formerly Mouse Tumor Biology (MTB)), Gene Ontology (GO)
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last database update
03/25/2025
MGI 6.24
The Jackson Laboratory