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Phenotypes associated with this allele
Allele Symbol
Allele Name
Allele ID
Gnl3tm2.1Rylt
targeted mutation 2.1, Robert Y L Tsai
MGI:5523416
Summary 3 genotypes
Jump to Allelic Composition Genetic Background Genotype ID
cn1
Gnl3tm2.1Rylt/Gnl3tm2.1Rylt
Tg(CAG-cre/Esr1*)5Amc/0
involves: 129 * 129S2/SvPas * C57BL/6 * CBA MGI:5523423
cn2
Gnl3tm2.1Rylt/Gnl3tm2.1Rylt
Trp53tm1Tyj/Trp53tm1Tyj
Tg(CAG-cre/Esr1*)5Amc/0
involves: 129 * 129S2/SvPas * C57BL/6 * CBA MGI:5523425
cn3
Gnl3tm2.1Rylt/Gnl3tm2.1Rylt
Tg(Nes-cre)1Kln/0
involves: 129 * C57BL/6 * CBA MGI:5523421


Genotype
MGI:5523423
cn1
Allelic
Composition
Gnl3tm2.1Rylt/Gnl3tm2.1Rylt
Tg(CAG-cre/Esr1*)5Amc/0
Genetic
Background
involves: 129 * 129S2/SvPas * C57BL/6 * CBA
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Gnl3tm2.1Rylt mutation (0 available); any Gnl3 mutation (56 available)
Tg(CAG-cre/Esr1*)5Amc mutation (10 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
cellular
• increase in the percentage of MEFs showing signs of replication-induced DNA damage after tamoxifen treatment
• tamoxifen treatment impairs the long-term proliferative potential of MEFs




Genotype
MGI:5523425
cn2
Allelic
Composition
Gnl3tm2.1Rylt/Gnl3tm2.1Rylt
Trp53tm1Tyj/Trp53tm1Tyj
Tg(CAG-cre/Esr1*)5Amc/0
Genetic
Background
involves: 129 * 129S2/SvPas * C57BL/6 * CBA
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Gnl3tm2.1Rylt mutation (0 available); any Gnl3 mutation (56 available)
Tg(CAG-cre/Esr1*)5Amc mutation (10 available)
Trp53tm1Tyj mutation (12 available); any Trp53 mutation (240 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
cellular
• increase in the percentage of MEFs showing signs of replication-induced DNA damage after tamoxifen treatment
• tamoxifen treatment shortens the lifespan of MEFs
• tamoxifen treatment impairs the long-term proliferative potential of MEFs




Genotype
MGI:5523421
cn3
Allelic
Composition
Gnl3tm2.1Rylt/Gnl3tm2.1Rylt
Tg(Nes-cre)1Kln/0
Genetic
Background
involves: 129 * C57BL/6 * CBA
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Gnl3tm2.1Rylt mutation (0 available); any Gnl3 mutation (56 available)
Tg(Nes-cre)1Kln mutation (4 available)
phenotype observed in females
phenotype observed in males
N normal phenotype

Severe brain defects in Gnl3tm2.1Rylt/Gnl3tm2.1Rylt Tg(Nes-cre)1Kln/0 embryos

mortality/aging

respiratory system

nervous system
• decrease in cellularity starting at E12.5
• increase in gamma-H2AFX protein in cells expressing this protein at E12.5
• major defects in the cerebellar primordium at E14.5 and E16.5
• major defects at E14.5 and E16.5
• smaller midbrain and hindbrain tegmentum at E14.5 and E16.5
• smaller at E14.5 and E16.5
• major defects in the cortex at E14.5 and E16.5
• major defects in the ganglionic eminence at E14.5 and E16.5
• decrease in neuronal stem cell numbers in the neuroepithelium at E12.5
• at E14.5 and E16.5

embryo
• decrease in cellularity starting at E12.5
• increase in gamma-H2AFX protein in cells expressing this protein at E12.5





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