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Phenotypes associated with this allele
Allele Symbol
Allele Name
Allele ID
Rarbtm1Vgi
targeted mutation 1, Vincent Giguere
MGI:2158691
Summary 2 genotypes
Jump to Allelic Composition Genetic Background Genotype ID
hm1
Rarbtm1Vgi/Rarbtm1Vgi involves: 129S1/Sv * 129X1/SvJ * C57BL/6 MGI:3618350
cx2
Rarbtm1Vgi/Rarbtm1Vgi
Rxrbtm1Rev/Rxrbtm1Rev
involves: 129S1/Sv * 129S4/SvJae * 129X1/SvJ * C57BL/6 MGI:3618351


Genotype
MGI:3618350
hm1
Allelic
Composition
Rarbtm1Vgi/Rarbtm1Vgi
Genetic
Background
involves: 129S1/Sv * 129X1/SvJ * C57BL/6
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Rarbtm1Vgi mutation (1 available); any Rarb mutation (39 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
behavior/neurological
• mutants display severe impairment in the Morris water maze test and show no improvement in performance over a training period of 8 days; after 24 hours mutants spend less time in the water where the platform had been in the previous trials compared to wild type controls

nervous system
• only transient depression of field excitatory postsynaptic potentials is observed in mutants in response to low frequency stimulation, while the controls show a long-lasting depression
• long term potentiation is absent in hippocampal slices from mutants
• long term depotentiation can not be induced in mutants

growth/size/body
• slightly but significantly decreased body weights are noted at P28
• however, no significant differences in body weight are observed at P42 and P56

respiratory system
• the gas-exchange surface area per cm3 of mutant lung tissue is reduced by ~30% at P28, P42 and P56
• impaired formation of the distal airspaces during the postnatal phase of lung maturation
• significantly reduced PDGFA protein levels are observed at P28, suggesting impaired postnatal lung alveolarization
• however, no differences in Pdgfra mRNA levels are observed at any postnatal age
• the volume density of airspace in the alveolar region of mutant lungs is significantly increased at P28, P42, and P56
• the mean cord length (Lm) of mutant respiratory airspaces is significantly increased only at P42
• however, the mean volume of individual alveoli, number of alveoli per cm3 of lung tissue, and distribution of alveolar volumes remain relatively normal at all postnatal time points studied
• no differences in the percentage of BrdU-labeled cells are noted in the alveolar region at any of time point
• no significant difference in the thickness of alveolar walls is observed at any time point
• alveolar ducts comprise a significantly greater proportion of mutant lung tissue at P28, P42, and P56
• alveolar sacs comprise a significantly greater proportion of mutant lung tissue at P28, P42, and P56
• carbon monoxide (CO) uptake is significantly reduced in mutant lungs at P56 when mice are at rest
• however, the pressure/volume characteristics of the lung are not significantly altered at this time point

cardiovascular system
• the gas-exchange surface area per cm3 of mutant lung tissue is reduced by ~30% at P28, P42 and P56




Genotype
MGI:3618351
cx2
Allelic
Composition
Rarbtm1Vgi/Rarbtm1Vgi
Rxrbtm1Rev/Rxrbtm1Rev
Genetic
Background
involves: 129S1/Sv * 129S4/SvJae * 129X1/SvJ * C57BL/6
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Rarbtm1Vgi mutation (1 available); any Rarb mutation (39 available)
Rxrbtm1Rev mutation (0 available); any Rxrb mutation (26 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
behavior/neurological
• mutants display severe impairment in the Morris water maze test and show no improvement in performance over a training period of 8 days; ater 24 hours mutants spend less time in the water where the platform had been in the previous trials compared to wild type controls

nervous system
• only transient depression of field excitatory postsynaptic potentials is observed in mutants in response to low frequency stimulation, while the controls show a long-lasting depression
• long term potentiation is absent in hippocampal slices from mutants
• long term depotentiation can not be induced in mutants





Contributing Projects:
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
04/16/2024
MGI 6.23
The Jackson Laboratory