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Phenotypes associated with this allele
Allele Symbol
Allele Name
Allele ID
Rlimtm1.2Inba
targeted mutation 1.2, Ingol Bach
MGI:4838154
Summary 2 genotypes
Jump to Allelic Composition Genetic Background Genotype ID
ht1
Rlimtm1.1Inba/Rlimtm1.2Inba involves: 129S1/Sv * 129X1/SvJ * C57BL/6 * FVB MGI:4838162
ot2
Rlimtm1.2Inba/Y involves: 129S1/Sv * 129X1/SvJ * C57BL/6 * FVB MGI:4838164


Genotype
MGI:4838162
ht1
Allelic
Composition
Rlimtm1.1Inba/Rlimtm1.2Inba
Genetic
Background
involves: 129S1/Sv * 129X1/SvJ * C57BL/6 * FVB
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Rlimtm1.1Inba mutation (0 available); any Rlim mutation (18 available)
Rlimtm1.2Inba mutation (0 available); any Rlim mutation (18 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
mortality/aging
• when the knock-out allele is maternally inherited, no female mice are recovered after E11.5
• however, male lethality is normal and paternal inheritance of the knock-out allele does not affect embryonic viability

reproductive system
• female mice cannot be produced from maternal transmission of the knock-out allele

embryo
• when the knock-out allele is maternally inherited, developmental abnormalities in female embryos occur as early as implantation or shortly thereafter
• when the knock-out allele is maternally inherited, most to all of the extraembryonic tissues derived from the extraembryonic trophoblast in female embryos is missing in the placenta unlike in wild-type mice
• however, maternal decidual is normal

cellular
• when the knock-out allele is maternally inherited, X inactivation of the paternal X chromosome is absent unlike in wild-type cells




Genotype
MGI:4838164
ot2
Allelic
Composition
Rlimtm1.2Inba/Y
Genetic
Background
involves: 129S1/Sv * 129X1/SvJ * C57BL/6 * FVB
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Rlimtm1.2Inba mutation (0 available); any Rlim mutation (18 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
normal phenotype
• mice are viable and fertile





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last database update
12/10/2024
MGI 6.24
The Jackson Laboratory