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Phenotypes associated with this allele
Allele Symbol
Allele Name
Allele ID
Tg(HBA1-GFP)1Ew
transgene insertion 1, Emma Whitelaw
MGI:3586533
Summary 13 genotypes
Jump to Allelic Composition Genetic Background Genotype ID
cx1
Foxo3mommeR1/Foxo3mommeR1
Tg(HBA1-GFP)1Ew/Tg(HBA1-GFP)1Ew
FVB/NJ-Foxo3mommeR1 Tg(HBA1-Gfp)1Ew MGI:4949205
cx2
Cdca7em1Ldax/Cdca7em1Ldax
Tg(HBA1-GFP)1Ew/0
FVB/NJ-Cdca7em1Ldax Tg(HBA1-GFP)1Ew MGI:7614332
cx3
Foxo3mommeR1/Foxo3tm1.1Rdp
Tg(HBA1-GFP)1Ew/0
involves: 129S6/SvEvTac * C57BL/6 * FVB/NJ MGI:4949206
cx4
Rif1MommeD18/Rif1+
Tg(HBA1-GFP)1Ew/Tg(HBA1-GFP)1Ew
involves: C57BL/6J * FVB/N MGI:5581680
cx5
Tg(HBA1-GFP)1Ew/Tg(HBA1-GFP)1Ew
WizMommeD30/WizMommeD30
involves: C57BL/6J * FVB/N MGI:5581678
cx6
Tg(HBA1-GFP)1Ew/Tg(HBA1-GFP)1Ew
WizMommeD30/Wiz+
involves: C57BL/6J * FVB/N MGI:5581679
cx7
Eif3hMommeD12/Eif3hMommeD38
Tg(HBA1-GFP)1Ew/0
involves: C57BL/6J * FVB/NJ MGI:5514392
cx8
Eif3hMommeD12/Eif3h+
Tg(HBA1-GFP)1Ew/0
involves: C57BL/6J * FVB/NJ MGI:5514388
cx9
Eif3hMommeD12/Eif3hMommeD12
Tg(HBA1-GFP)1Ew/0
involves: C57BL/6J * FVB/NJ MGI:5514389
cx10
Eif3hMommeD38/Eif3h+
Tg(HBA1-GFP)1Ew/0
involves: C57BL/6J * FVB/NJ MGI:5514390
cx11
Eif3hMommeD38/Eif3hMommeD38
Tg(HBA1-GFP)1Ew/0
involves: C57BL/6J * FVB/NJ MGI:5514391
cx12
Dnmt3bMommeD14/Dnmt3btm1Enl
Tg(HBA1-GFP)1Ew/0
involves: FVB/N MGI:5515792
cx13
Dnmt3bMommeD14/Dnmt3bMommeD14
Tg(HBA1-GFP)1Ew/0
involves: FVB/N MGI:5515788


Genotype
MGI:4949205
cx1
Allelic
Composition
Foxo3mommeR1/Foxo3mommeR1
Tg(HBA1-GFP)1Ew/Tg(HBA1-GFP)1Ew
Genetic
Background
FVB/NJ-Foxo3mommeR1 Tg(HBA1-Gfp)1Ew
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Foxo3mommeR1 mutation (2 available); any Foxo3 mutation (48 available)
Tg(HBA1-GFP)1Ew mutation (0 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
cellular
• at P3 some primordial follicles show an increase in the size of primary oocytes
• oocytes are less likely to have a polar body on ovulation

reproductive system
• oocytes are less likely to have a polar body on ovulation
• at 18 weeks of age
• at P30 compared to heterozygous controls
• in some ovaries a disproportionate increase in oocyte size relative to the follicular cells is seen at P30
• increase in the number of follicles at P30
• marked decrease in the number of primary follicles at P60
• increase in the number of secondary follicles at P30
• at 18 weeks of age ovarian follicles are absent in 3 of 4 mice and the remaining mouse has a few degenerating primordial follicles
• at P3 some primordial follicles show an increase in the size of primary oocytes
• at P14 most of the remaining primordial follicles contain an enlarged primary oocyte surrounded by spindle-shaped/squamous follicular cells
• marked decrease in the number of primordial follicles at P60
• at 18 weeks of age 1 of 4 mice has a few degenerating primordial follicles
• at P30 compared to heterozygous controls
• at 1 year of age occasional females have grossly enlarged ovaries
• found in grossly enlarged ovaries at 1 year of age
• Background Sensitivity: teratomas are seen in about 1 in 6 mice of aged up to 8 months in mice on an FVB/NJ background but not in mice on an inbred C57BL/6J background
• apparent asynchronous development of the oocyte and follicle
• females lose fertility by about 8 weeks of age
• however, males display normal fertility
• apparent asynchronous development of the oocyte and follicle
• at P3 some primordial follicles show an increase in the size of primary oocytes
• oocytes from superovulated females are less likely to have a polar body on the day of ovulation
• increased proportion of superovulated oocytes that are arrested at metaphase of meiosis I
• oocytes cultured overnight are more likely to fragment than those from superovulated heterozygous females

neoplasm
• found in grossly enlarged ovaries at 1 year of age
• Background Sensitivity: teratomas are seen in about 1 in 6 mice of aged up to 8 months in mice on an FVB/NJ background but not in mice on an inbred C57BL/6J background

growth/size/body
• at P30 compared to heterozygous controls
• at 1 year of age occasional females have grossly enlarged ovaries

mortality/aging
• females lose fertility by about 8 weeks of age
• however, males display normal fertility

endocrine/exocrine glands
• at 18 weeks of age
• at P30 compared to heterozygous controls
• in some ovaries a disproportionate increase in oocyte size relative to the follicular cells is seen at P30
• increase in the number of follicles at P30
• marked decrease in the number of primary follicles at P60
• increase in the number of secondary follicles at P30
• at 18 weeks of age ovarian follicles are absent in 3 of 4 mice and the remaining mouse has a few degenerating primordial follicles
• at P3 some primordial follicles show an increase in the size of primary oocytes
• at P14 most of the remaining primordial follicles contain an enlarged primary oocyte surrounded by spindle-shaped/squamous follicular cells
• marked decrease in the number of primordial follicles at P60
• at 18 weeks of age 1 of 4 mice has a few degenerating primordial follicles
• at P30 compared to heterozygous controls
• at 1 year of age occasional females have grossly enlarged ovaries
• found in grossly enlarged ovaries at 1 year of age
• Background Sensitivity: teratomas are seen in about 1 in 6 mice of aged up to 8 months in mice on an FVB/NJ background but not in mice on an inbred C57BL/6J background
• apparent asynchronous development of the oocyte and follicle

Mouse Models of Human Disease
DO ID OMIM ID(s) Ref(s)
dermoid cyst of ovary DOID:5117 OMIM:166950
J:170710




Genotype
MGI:7614332
cx2
Allelic
Composition
Cdca7em1Ldax/Cdca7em1Ldax
Tg(HBA1-GFP)1Ew/0
Genetic
Background
FVB/NJ-Cdca7em1Ldax Tg(HBA1-GFP)1Ew
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Cdca7em1Ldax mutation (0 available); any Cdca7 mutation (27 available)
Tg(HBA1-GFP)1Ew mutation (0 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
cellular
• lower levels of chromatin-bound CDCA7 protein in E10.5 embryos
• higher percentage of erythrocytes expressing Tg(HBA1-GFP)1Ew transgene at age P21
• lower transgene Tg(HBA1-GFP)1Ew DNA methylation levels at age P21
• global DNA hypomethylation in spleen, thymus, cerebrum and liver at age P21
• DNA hypomethylation of minor satellite repeats and intracisternal A particle (IAP) retrotransposons in spleen, thymus and liver at age P21
• normal DNA methylation of major satellite repeats in spleen, thymus and liver at age P21

embryo
N
• mice born at expected Mendelian ratios

growth/size/body
N
• no obvious phenotype

mortality/aging
N
• viable
• mice present at expected Mendelian ratios at age P21




Genotype
MGI:4949206
cx3
Allelic
Composition
Foxo3mommeR1/Foxo3tm1.1Rdp
Tg(HBA1-GFP)1Ew/0
Genetic
Background
involves: 129S6/SvEvTac * C57BL/6 * FVB/NJ
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Foxo3mommeR1 mutation (2 available); any Foxo3 mutation (48 available)
Foxo3tm1.1Rdp mutation (1 available); any Foxo3 mutation (48 available)
Tg(HBA1-GFP)1Ew mutation (0 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
reproductive system
• marked reduction in the number of primary follicles in some mice at 12 weeks of age
• marked reduction in the number of primordial follicles in some mice at 12 weeks of age
• in some mice at 12 weeks of age

neoplasm
N
• unlike mice homozygous for Foxo3mommeR1 no ovarian teratomas are detected (in 7 mice)

endocrine/exocrine glands
• marked reduction in the number of primary follicles in some mice at 12 weeks of age
• marked reduction in the number of primordial follicles in some mice at 12 weeks of age
• in some mice at 12 weeks of age




Genotype
MGI:5581680
cx4
Allelic
Composition
Rif1MommeD18/Rif1+
Tg(HBA1-GFP)1Ew/Tg(HBA1-GFP)1Ew
Genetic
Background
involves: C57BL/6J * FVB/N
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Rif1MommeD18 mutation (0 available); any Rif1 mutation (172 available)
Tg(HBA1-GFP)1Ew mutation (0 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
cellular




Genotype
MGI:5581678
cx5
Allelic
Composition
Tg(HBA1-GFP)1Ew/Tg(HBA1-GFP)1Ew
WizMommeD30/WizMommeD30
Genetic
Background
involves: C57BL/6J * FVB/N
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Tg(HBA1-GFP)1Ew mutation (0 available)
WizMommeD30 mutation (0 available); any Wiz mutation (60 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
mortality/aging




Genotype
MGI:5581679
cx6
Allelic
Composition
Tg(HBA1-GFP)1Ew/Tg(HBA1-GFP)1Ew
WizMommeD30/Wiz+
Genetic
Background
involves: C57BL/6J * FVB/N
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Tg(HBA1-GFP)1Ew mutation (0 available)
WizMommeD30 mutation (0 available); any Wiz mutation (60 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
cellular




Genotype
MGI:5514392
cx7
Allelic
Composition
Eif3hMommeD12/Eif3hMommeD38
Tg(HBA1-GFP)1Ew/0
Genetic
Background
involves: C57BL/6J * FVB/NJ
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Eif3hMommeD12 mutation (0 available); any Eif3h mutation (32 available)
Eif3hMommeD38 mutation (0 available); any Eif3h mutation (32 available)
Tg(HBA1-GFP)1Ew mutation (0 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
mortality/aging
• no mice are present at weaning




Genotype
MGI:5514388
cx8
Allelic
Composition
Eif3hMommeD12/Eif3h+
Tg(HBA1-GFP)1Ew/0
Genetic
Background
involves: C57BL/6J * FVB/NJ
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Eif3hMommeD12 mutation (0 available); any Eif3h mutation (32 available)
Tg(HBA1-GFP)1Ew mutation (0 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
cellular




Genotype
MGI:5514389
cx9
Allelic
Composition
Eif3hMommeD12/Eif3hMommeD12
Tg(HBA1-GFP)1Ew/0
Genetic
Background
involves: C57BL/6J * FVB/NJ
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Eif3hMommeD12 mutation (0 available); any Eif3h mutation (32 available)
Tg(HBA1-GFP)1Ew mutation (0 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
mortality/aging
• only empty deciduas are present at E9.5

reproductive system




Genotype
MGI:5514390
cx10
Allelic
Composition
Eif3hMommeD38/Eif3h+
Tg(HBA1-GFP)1Ew/0
Genetic
Background
involves: C57BL/6J * FVB/NJ
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Eif3hMommeD38 mutation (0 available); any Eif3h mutation (32 available)
Tg(HBA1-GFP)1Ew mutation (0 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
cellular




Genotype
MGI:5514391
cx11
Allelic
Composition
Eif3hMommeD38/Eif3hMommeD38
Tg(HBA1-GFP)1Ew/0
Genetic
Background
involves: C57BL/6J * FVB/NJ
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Eif3hMommeD38 mutation (0 available); any Eif3h mutation (32 available)
Tg(HBA1-GFP)1Ew mutation (0 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
mortality/aging
• only empty deciduas are present at E9.5

reproductive system




Genotype
MGI:5515792
cx12
Allelic
Composition
Dnmt3bMommeD14/Dnmt3btm1Enl
Tg(HBA1-GFP)1Ew/0
Genetic
Background
involves: FVB/N
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Dnmt3bMommeD14 mutation (0 available); any Dnmt3b mutation (50 available)
Dnmt3btm1Enl mutation (1 available); any Dnmt3b mutation (50 available)
Tg(HBA1-GFP)1Ew mutation (0 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
cellular
• compound heterozygous mice display a higher percentage of GFP-expressing cells than heterozygotes
• significantly reduced methylation of transgene DNA in homozygous individuals (28 % of CpGs methylated) compared with wild type littermates (62 % of CpGs methylated), consistent with the change in transcriptional activity

growth/size/body
• hypotelorism and other cranial defects are seen, similar to phenotypes of other alleles of this gene
• small in stature




Genotype
MGI:5515788
cx13
Allelic
Composition
Dnmt3bMommeD14/Dnmt3bMommeD14
Tg(HBA1-GFP)1Ew/0
Genetic
Background
involves: FVB/N
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Dnmt3bMommeD14 mutation (0 available); any Dnmt3b mutation (50 available)
Tg(HBA1-GFP)1Ew mutation (0 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
cellular
• surviving homozygous mice displayed a higher percentage of GFP-expressing cells than did the heterozygotes
• significantly reduced methylation of transgene DNA in homozygous individuals (28 % of CpGs methylated) compared with wild type littermates (62 % of CpGs methylated), consistent with the change in transcriptional activity

mortality/aging
• heterozygous intercrosses only resulted in 10% of homozygous offspring instead of the expected 25%





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