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Phenotypes Associated with This Genotype
Genotype
MGI:2653523
Allelic
Composition
Nrg1tm1Cbm/Nrg1tm3Cbm
Isl1tm1(cre)Tmj/Isl1+
Genetic
Background
involves: 129P2/OlaHsd * 129X1/SvJ
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Isl1tm1(cre)Tmj mutation (0 available); any Isl1 mutation (38 available)
Nrg1tm1Cbm mutation (0 available); any Nrg1 mutation (56 available)
Nrg1tm3Cbm mutation (0 available); any Nrg1 mutation (56 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
muscle
• mutants exhibit a defect in muscle spindle differentiation in the dorsal root ganglion and motor neurons

nervous system
• selective absence of Schwann cells at E16.5 in adductor and gracilis muscles but not in other muscles
• mutants exhibit a defect in muscle spindle differentiation in the dorsal root ganglion and motor neurons
• parvalbumin+ proprioceptive afferents are present in E16.5 hindlimb muscles and initiate contact with individual myofibers, but they do not develop annulospiral branches around the myofibers
• parvalbumin+ proprioceptive terminals at muscle spindles remain primitive and unbranched at E18.5
• however, survival and initial differentiation of proprioceptive afferent sensory neurons is not impaired

cellular
• selective absence of Schwann cells at E16.5 in adductor and gracilis muscles but not in other muscles


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
12/30/2025
MGI 6.24
The Jackson Laboratory