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Phenotypes Associated with This Genotype
Genotype
MGI:3603467
Allelic
Composition
Ighmbp2nmd-2J/Ighmbp2nmd-2J
Genetic
Background
BKS.Cg Dock7m +/+ Leprdb-Ighmbp2nmd-2J
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Ighmbp2nmd-2J mutation (5 available); any Ighmbp2 mutation (46 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
mortality/aging
• death usually by 3.5 weeks although survival for several months is possible if left with parents without normal siblings present

behavior/neurological
• clench hindlimbs when picked up by the tail
• unable to grasp cage cover when set upon it
• rely on forelimbs to crawl forward, but balance and righting responses are normal
• dorsally contracted hindlimbs cannot be extended to stand erect or assume full posture on four limbs

muscle
• atrophic muscle fibers in the masseter
• atrophic muscle fibers in the temporalis muscle
• intermixture of very small muscle fibers with more normal fibers
• distal musculature of limbs more severely affected but focal areas of muscle degeneration proximally as well

nervous system
• affected alpha motor neurons with pale staining nuclei and perikarya
• mostly in lumbar region

craniofacial
• atrophic muscle fibers in the masseter
• atrophic muscle fibers in the temporalis muscle

growth/size/body
• atrophic muscle fibers in the masseter
• atrophic muscle fibers in the temporalis muscle


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