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Phenotypes associated with this allele
Allele Symbol
Allele Name
Allele ID
Raxtm1.1(cre/ERT2)Sbls
targeted mutation 1.1, Seth Blackshaw
MGI:5558909
Summary 1 genotype
Jump to Allelic Composition Genetic Background Genotype ID
cn1
Raxtm1.1(cre/ERT2)Sbls/Rax+
Yap1tm1Hmc/Yap1tm1Hmc
involves: 129S6/SvEvTac * C57BL/6NCrl MGI:6716882


Genotype
MGI:6716882
cn1
Allelic
Composition
Raxtm1.1(cre/ERT2)Sbls/Rax+
Yap1tm1Hmc/Yap1tm1Hmc
Genetic
Background
involves: 129S6/SvEvTac * C57BL/6NCrl
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Raxtm1.1(cre/ERT2)Sbls mutation (1 available); any Rax mutation (16 available)
Yap1tm1Hmc mutation (0 available); any Yap1 mutation (37 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
vision/eye
• S-opsin and M-cone opsins are reduced in the retina, with S-opsin signal drastically decreased dorsally while M-opsin almost absent ventrally
• however, the number of cones is not changed
• 4-OHT-treated mice show reactive gliosis in the retina at 12 months of age

nervous system
• marker analysis of mice treated with 4-hydroxy-tamoxifen (4-OHT) at P10 shows Muller cell homeostasis dysfunction at 12 months of age





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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
05/14/2024
MGI 6.23
The Jackson Laboratory