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Phenotypes associated with this allele
Allele Symbol
Allele Name
Allele ID
Rb1tm1Dwg
targeted mutation 1, David W Goodrich
MGI:3617652
Summary 3 genotypes
Jump to Allelic Composition Genetic Background Genotype ID
hm1
Rb1tm1Dwg/Rb1tm1Dwg involves: 129/Sv * C57BL/6 MGI:3618355
ht2
Rb1tm1Dwg/Rb1tm1Tyj involves: 129/Sv * 129S2/SvPas * C57BL/6 MGI:3618362
cn3
Rb1tm1Dwg/Rb1tm2Brn
Tg(Chx10-EGFP/cre,-ALPP)2Clc/0
involves: 129/Sv * C57BL/6 * SJL MGI:3618365


Genotype
MGI:3618355
hm1
Allelic
Composition
Rb1tm1Dwg/Rb1tm1Dwg
Genetic
Background
involves: 129/Sv * C57BL/6
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Rb1tm1Dwg mutation (0 available); any Rb1 mutation (106 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
mortality/aging
• a few live homozygotes can be recovered as late as E17.5 (2 of 18 viable), indicating that mutants survive at least 2 days longer than homozygous Rb1tm1Tyj mice

cellular
• MEFs exhibit an increase in the fraction of cells in the S and G2/M phases of the cell cycle
• MEFs fail to efficiently trigger G1/S cell cycle arrest in response to DNA damage
• apoptosis is detected in the lens fiber compartment that is not seen in wild-type
• MEFs cultured at confluence exhibit an increase in cell proliferation compared to wild-type MEFs

embryo
• although embryos are smaller than wild-type, they are larger than age-matched homozygous Rb1tm1Tyj embryos
• normal labyrinth architecture is disrupted
• the porous appearance of the labyrinth layer is absent
• exhibit defective placental transport as indicated by a 7.7% reduction of the essential fatty acid linoleic acid, arachidonic acid and docosahexaenoic acid in E14.5 embryos relative to wild-type

hematopoietic system
• small percentage of erythrocytes exhibit enucleating defects at E17.5, indicating a less severe erythrocyte maturation defect than seen in homozygous Rb1tm1Tyj mice
• fetal liver macrophages show fewer defects in differentiation compared to homozygous Rb1tm1Tyj mice

vision/eye
• apoptosis is detected in the lens fiber compartment that is not seen in wild-type
• detect ectopic mitoses in the lens fiber compartment that is not seen in wild-type
• lens fiber cells are disorganized

nervous system
• detect ectopic mitosis and apoptosis in the intermediate zones of the fourth ventricle
• detect ectopic mitosis and apoptosis in the intermediate zones of the third ventricle
• detect ectopic mitosis and apoptosis in the trigeminal ganglia
• detect ectopic mitosis and apoptosis in the dorsal root ganglia

immune system
• fetal liver macrophages show fewer defects in differentiation compared to homozygous Rb1tm1Tyj mice

growth/size/body
• although embryos are smaller than wild-type, they are larger than age-matched homozygous Rb1tm1Tyj embryos

integument
• although embryos are paler than wild-type, they exhibit improved coloration over that seen in homozygous Rb1tm1Tyj embryos




Genotype
MGI:3618362
ht2
Allelic
Composition
Rb1tm1Dwg/Rb1tm1Tyj
Genetic
Background
involves: 129/Sv * 129S2/SvPas * C57BL/6
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Rb1tm1Dwg mutation (0 available); any Rb1 mutation (106 available)
Rb1tm1Tyj mutation (5 available); any Rb1 mutation (106 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
mortality/aging
• survive as long as homozygous Rb1tm1Dwg mice, with 2 of 18 dead at E15.5 and 4 of 7 dead at E17.5

growth/size/body
• although embryos are smaller than wild-type, they are larger than age-matched homozygous Rb1tm1Tyj embryos

hematopoietic system
• small percentage of erythrocytes exhibit enucleating defects at E17.5, indicating a less severe erythrocyte maturation defect than seen in homozygous Rb1tm1Tyj mice

embryo
• although embryos are smaller than wild-type, they are larger than age-matched homozygous Rb1tm1Tyj embryos

integument
• although embryos are paler than wild-type, they exhibit improved coloration over that seen in homozygous Rb1tm1Tyj embryos




Genotype
MGI:3618365
cn3
Allelic
Composition
Rb1tm1Dwg/Rb1tm2Brn
Tg(Chx10-EGFP/cre,-ALPP)2Clc/0
Genetic
Background
involves: 129/Sv * C57BL/6 * SJL
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Rb1tm1Dwg mutation (0 available); any Rb1 mutation (106 available)
Rb1tm2Brn mutation (3 available); any Rb1 mutation (106 available)
Tg(Chx10-EGFP/cre,-ALPP)2Clc mutation (1 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
vision/eye
• significant reduction in rod photoreceptors at P14, however no changes in the number of other major cell types in the retina
• horizontal cell synaptogenesis in the retina is defective

nervous system
• significant reduction in rod photoreceptors at P14, however no changes in the number of other major cell types in the retina
• horizontal cell synaptogenesis in the retina is defective





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last database update
04/16/2024
MGI 6.23
The Jackson Laboratory