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Phenotypes associated with this allele
Allele Symbol
Allele Name
Allele ID
Rfx3tm1.1Wrth
targeted mutation 1.1, W Reith
MGI:3045792
Summary 2 genotypes
Jump to Allelic Composition Genetic Background Genotype ID
hm1
Rfx3tm1.1Wrth/Rfx3tm1.1Wrth involves: 129 * C57BL/6J MGI:3045840
ht2
Rfx3tm1.1Wrth/Rfx3+ involves: 129 * C57BL/6J MGI:3045842


Genotype
MGI:3045840
hm1
Allelic
Composition
Rfx3tm1.1Wrth/Rfx3tm1.1Wrth
Genetic
Background
involves: 129 * C57BL/6J
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Rfx3tm1.1Wrth mutation (0 available); any Rfx3 mutation (68 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
mortality/aging
• two thirds of those that survive past E12 die at birth
• half of the homozygous mutant embryos die around E11 - E12

cardiovascular system
• at E10.5 inversion of cardiac looping is seen in 19% of mutant embryos
• at E18, 6 out of 10 mutant embryos had meso- or dextrocardia
• at E18, 6 out of 10 mutant embryos had meso- or dextrocardia

embryo
• from E7.25 to E8.0 growth of nodal cilia is significantly delayed resulting in significantly shorter cilia in homozygous embryos
• at E10.5 inversion of embryo turning is seen in 19% of mutant embryos
• markers that are normally expressed only on the left side are expressed on both sides

growth/size/body
• mutants are about two thirds the size of wild-type littermates at birth
• growth retardation increases as the mutant mice age with adults body weight being about half that of control littermates
• 6% of those mutants that survive past birth have situs inversus
• at E18, 6% of mutant embryos had situs inversus and 29% had incomplete inversion defects

cellular
• from E7.25 to E8.0 growth of nodal cilia is significantly delayed resulting in significantly shorter cilia in homozygous embryos




Genotype
MGI:3045842
ht2
Allelic
Composition
Rfx3tm1.1Wrth/Rfx3+
Genetic
Background
involves: 129 * C57BL/6J
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Rfx3tm1.1Wrth mutation (0 available); any Rfx3 mutation (68 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
growth/size/body
• slight growth retardation is seen in heterozygotes compared to control littermates





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last database update
11/19/2024
MGI 6.24
The Jackson Laboratory