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Phenotypes associated with this allele
Allele Symbol
Allele Name
Allele ID
Nr3c1tm3Gsc
targeted mutation 3, Gunther Schutz
MGI:1931329
Summary 3 genotypes
Jump to Allelic Composition Genetic Background Genotype ID
hm1
Nr3c1tm3Gsc/Nr3c1tm3Gsc involves: 129P2/OlaHsd MGI:3817858
hm2
Nr3c1tm3Gsc/Nr3c1tm3Gsc involves: 129P2/OlaHsd * C57BL/6 MGI:2175166
hm3
Nr3c1tm3Gsc/Nr3c1tm3Gsc involves: 129P2/OlaHsd * FVB/N MGI:4455054


Genotype
MGI:3817858
hm1
Allelic
Composition
Nr3c1tm3Gsc/Nr3c1tm3Gsc
Genetic
Background
involves: 129P2/OlaHsd
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Nr3c1tm3Gsc mutation (1 available); any Nr3c1 mutation (35 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
hematopoietic system
• E14.5 fetal liver cultures fail to exhibit outgrowths of erythroid progenitor cells as do wild-type livers
• mice treated with phenylhydrazine to induce anemia or exposed to hypoxic conditions fail to exhibit an increase in colony forming unit-erythroid cells unlike in similarly treated wild-type mice
• fetal liver cells transplanted into irradiated wild-type mice fail to respond normally with increased erythroid progenitor cell numbers to hypoxic conditions




Genotype
MGI:2175166
hm2
Allelic
Composition
Nr3c1tm3Gsc/Nr3c1tm3Gsc
Genetic
Background
involves: 129P2/OlaHsd * C57BL/6
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Nr3c1tm3Gsc mutation (1 available); any Nr3c1 mutation (35 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
homeostasis/metabolism
• elevated serum level of corticosterone




Genotype
MGI:4455054
hm3
Allelic
Composition
Nr3c1tm3Gsc/Nr3c1tm3Gsc
Genetic
Background
involves: 129P2/OlaHsd * FVB/N
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Nr3c1tm3Gsc mutation (1 available); any Nr3c1 mutation (35 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
skeleton
N
• bone formation with prednisolone treatment for 2 weeks is repressed in controls and mutants; bone mass and trabecular thickness as well as strong reduction in osteoblast and osteocyte numbers and osteoblast surface area are observed in controls and experimental animals with inhibition of bone formation by prednisolone
• dexamethasone-induced apoptosis is observed in cultured mutant and wild-type cells
• in dexamethasone-treated cultures, postconfluential cell numbers are slightly decreased, similar to wild-type cultures
• alkaline phosphatase activity and matrix mineralization are inhibited by dexamethasone treatment in mutant and wild-type cultures
• basal osteoclastogenesis is not affected in mutant cell culture; dexamethasone suppresses osteoclastogenesis similary in mutant and wild-type cultures
• proliferation of preconfluent preosteoblasts from neonatal calvaria is lower in culture compared to wild-type cells
• treatment with dexamethasone does not affect mutant cells but completely inhibits osteoblast proliferation in cultures of wild-type cells

cellular
• proliferation of preconfluent preosteoblasts from neonatal calvaria is lower in culture compared to wild-type cells
• treatment with dexamethasone does not affect mutant cells but completely inhibits osteoblast proliferation in cultures of wild-type cells





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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
11/12/2024
MGI 6.24
The Jackson Laboratory