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Phenotypes Associated with This Genotype
Genotype
MGI:3806032
Allelic
Composition
L1camtm1Sor/Y
Nrcamtm1Gmt/Nrcamtm1Gmt
Genetic
Background
involves: 129S6/SvEvTac * 129S7/SvEvBrd * Swiss Webster
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
L1camtm1Sor mutation (2 available); any L1cam mutation (12 available)
Nrcamtm1Gmt mutation (1 available); any Nrcam mutation (87 available)
phenotype observed in females
phenotype observed in males
N normal phenotype

Cerebellar abnormalities in L1camtm1Sor/Y Nrcamtm1Gmt/Nrcamtm1Gmt mice

mortality/aging
• do not detect any mutants at P8

growth/size/body
• body weights of pups are 40-70% of control littermates at P3-P6

nervous system
• cerebellar dysgenesis
• cerebellar fissures are less developed
• thickness of the inner granule layer is reduced by 40-50%
• marker analysis indicates defects in foliation
• thickness of the external granule layer is reduced by 10-30%
• cerebellar lobes are less developed
• marker analysis indicates possible defects in granule cells during cerebellar development
• thickness of the inner granule layer is reduced by 40-50%
• thickness of the external granule layer is reduced by 10-30%


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
06/12/2024
MGI 6.13
The Jackson Laboratory