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Phenotypes Associated with This Genotype
Genotype
MGI:5545905
cn5
Allelic
Composition
Rnf7tm1c(EUCOMM)Wtsi/Rnf7tm1c(EUCOMM)Wtsi
Tg(Nes-cre)1Kln/0
Genetic
Background
involves: C57BL/6 * C57BL/6N * SJL
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Rnf7tm1c(EUCOMM)Wtsi mutation (0 available); any Rnf7 mutation (15 available)
Tg(Nes-cre)1Kln mutation (4 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
nervous system
• fewer mitotic granule cell in the cerebellum at P5
• progressive in most mice by 3 to 6 months
• in most mice at P10 to P15
• ectopic lamination at E17.5
• intermingling layers at P5
• at E17.5
• in the white matter at P5
• reduced area at P5

growth/size/body
• mice fail to thrive

cellular
• fewer mitotic granule cell in the cerebellum at P5


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
03/24/2026
MGI 6.24
The Jackson Laboratory