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Phenotypes Associated with This Genotype
Genotype
MGI:3618312
Allelic
Composition
Cntftm1Mpin/Cntftm1Mpin
Genetic
Background
involves: 129S2/SvPas
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Cntftm1Mpin mutation (1 available); any Cntf mutation (16 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
nervous system
• atrophic and degenerative changes in spinal motor neurons are accompanied by an increase in the numbers of activated microglial cells
• at 8 weeks of age, lumbar motor neuron cell bodies are smaller and the nuclei are swollen, resulting in an increase in the ratio between nuclear and cytoplasmic areas of about 40%, however by 14 weeks of age, both cell area and nuclear area are smaller
• 22% reduction in facial motor neurons at 28 weeks of age but not at 4 weeks of age
• with increasing age, spinal motor neurons exhibit progressive atrophy and finally degeneration
• trophy becomes apparent by 8 weeks of age and the first signs of degeneration are seen at 22 weeks of age

muscle
• small but significant reduction in muscle strength at 28 weeks of age, as indicated by forelimb grip strength

behavior/neurological
• small but significant reduction in forelimb grip strength at 28 weeks of age

hematopoietic system
• atrophic and degenerative changes in spinal motor neurons are accompanied by an increase in the numbers of activated microglial cells

immune system
• atrophic and degenerative changes in spinal motor neurons are accompanied by an increase in the numbers of activated microglial cells

cellular
• atrophic and degenerative changes in spinal motor neurons are accompanied by an increase in the numbers of activated microglial cells


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
01/28/2026
MGI 6.24
The Jackson Laboratory