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Phenotypes Associated with This Genotype
Genotype
MGI:5614114
Allelic
Composition
Rbl1tm1.1Fad/Rbl1tm1.1Fad
Rbl2tm1Tyj/Rbl2tm1Tyj
Genetic
Background
involves: 129S2/SvPas * C57BL/6 * FVB/N
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Rbl1tm1.1Fad mutation (1 available); any Rbl1 mutation (58 available)
Rbl2tm1Tyj mutation (1 available); any Rbl2 mutation (51 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
cellular
N
• proliferating and serum starved cells exhibit normal withdrawal from the cell cycle

craniofacial
• small and underdeveloped
• small and underdeveloped

growth/size/body
• despite normal weight at E18.5, rare survivors are severely runted

hearing/vestibular/ear

limbs/digits/tail
• at E18.5
• at E18.5
• at E18.5
• at E18.5
• at E18.5

mortality/aging
• all but one mouse died by 1.5 days after birth
• some mice die shortly after birth

skeleton
• small and underdeveloped
• small and underdeveloped
• hyperplasia of chondrocytes in the resting and proliferating zones
• hyperplasia of chondrocytes in the resting and proliferating zones
• at E18.5
• at E18.5
• at E18.5
• at E18.5
• at E18.5
• poorly mineralized inner ear ossicles
• however, mineralization of the long bones is normal


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
03/18/2025
MGI 6.24
The Jackson Laboratory