cardiovascular system
• very mild in some mice
|
nervous system
• very mild in some mice
|
Allele Symbol Allele Name Allele ID |
Tgfb1tm1Jmu targeted mutation 1, John Munger MGI:3513111 |
||||||||||||||||||||||||||||||||||||||||||||
Summary |
10 genotypes
|
|
|
♀ | phenotype observed in females |
♂ | phenotype observed in males |
N | normal phenotype |
• very mild in some mice
|
• very mild in some mice
|
|
|
♀ | phenotype observed in females |
♂ | phenotype observed in males |
N | normal phenotype |
• mice have reduced survival
|
• while Mendelian ratios are present at E10.5, fewer than expected pups are born
|
• between 18 and 28 days, marked mononuclear cell infiltration of multiple tissues, in particular, the heart, lung, liver, stomach, and pancreas and occasionally the central nervous system
|
• inflammation lesions in the liver are localized to the portal canal
|
• in the lung, inflammatory lesions are usually localized to bronchi and larger vessels and sometimes diffusely within the alveolar walls
|
• at E10.5, yolk sacs lack normal vasculature
• at E12.5, yolk sac vasculature is not identifiable
|
• at E10.5, yolk sacs have a variable paucity of vessels, absence of hemotopoietic cells and extensive buckling between the mesodermal and endodermal layer
|
• at E10.5, yolk sacs have extensive buckling between the mesodermal and endodermal layer
|
• at E10.5, yolk sacs are anemic or lacking normal vasculature
|
• at day 14, mice are smaller in size
|
• inflammation lesions in the liver are localized to the portal canal
|
• in the lung, inflammatory lesions are usually localized to bronchi and larger vessels and sometimes diffusely within the alveolar walls
|
• at E10.5, yolk sacs lack normal vasculature
• at E12.5, yolk sac vasculature is not identifiable
|
|
|
♀ | phenotype observed in females |
♂ | phenotype observed in males |
N | normal phenotype |
• phenotype is indistinguishable from that seen on a 129S6/SvEvTac C57BL/6 background
|
• phenotype is indistinguishable from that seen on a 129S6/SvEvTac C57BL/6 background
|
• phenotype is indistinguishable from that seen on a 129S6/SvEvTac C57BL/6 background
|
• phenotype is indistinguishable from that seen on a 129S6/SvEvTac C57BL/6 background
|
• phenotype is indistinguishable from that seen on a 129S6/SvEvTac C57BL/6 background
|
• phenotype is indistinguishable from that seen on a 129S6/SvEvTac C57BL/6 background
|
|
|
♀ | phenotype observed in females |
♂ | phenotype observed in males |
N | normal phenotype |
• while Mendelian ratios are present at E10.5, fewer than expected pups are born
|
|
|
♀ | phenotype observed in females |
♂ | phenotype observed in males |
N | normal phenotype |
• very few mice are born
• Background Sensitivity: fewer mice are born than on a background lacking BALB/c or containing ICR
|
• in all mice
|
• in all mice
|
|
|
♀ | phenotype observed in females |
♂ | phenotype observed in males |
N | normal phenotype |
• most mice only survive 3 weeks before dying of widespread inflammation
|
• rarely
|
• rarely
|
|
|
♀ | phenotype observed in females |
♂ | phenotype observed in males |
N | normal phenotype |
N |
• Background Sensitivity: more mice are born on a background containing ICR than on a background containing BALB/c or lacking both ICR and BALB/c
|
• all mice die within hours of birth
|
• as early as E11.5
• at E13.5, brain vasculature exhibits extensive cavitation compared to in control mice
• in newborn mice, brain vessels are enlarged and hyperplastic compared to in control mice
|
• as early as E11.5
• severe by E15.5
• in all mice
|
• associated with brain hemorrhage
|
• enlarged ventricles
|
• as early as E11.5
• at E13.5, brain vasculature exhibits extensive cavitation compared to in control mice
• in newborn mice, brain vessels are enlarged and hyperplastic compared to in control mice
|
• as early as E11.5
• severe by E15.5
• in all mice
|
• more extensive complete cleft of the secondary palate compared to in Tgfb3tm1Doe homozygotes on the same background
|
N |
• mice exhibit normal lung morphology
|
• more extensive complete cleft of the secondary palate compared to in Tgfb3tm1Doe homozygotes on the same background
|
• more extensive complete cleft of the secondary palate compared to in Tgfb3tm1Doe homozygotes on the same background
|
|
|
♀ | phenotype observed in females |
♂ | phenotype observed in males |
N | normal phenotype |
• most mice only survive 3 weeks before dying of widespread inflammation
|
• in newborn mice, brain vasculature exhibits cavitation compared to in control mice
|
• in all newborn mice
• less severe than in double homozygotes
|
• in newborn mice, brain vasculature exhibits cavitation compared to in control mice
|
• in all newborn mice
• less severe than in double homozygotes
|
• in newborn mice
|
|
|
♀ | phenotype observed in females |
♂ | phenotype observed in males |
N | normal phenotype |
• very few mice are born
• Background Sensitivity: more mice are born than on a background lacking BALB/c, but fewer mice are born than on a background containing ICR
|
• most mice die between E8.5 and E12.5
|
• in non-viable mice
|
• in all mice
|
• in non-viable mice
|
• in all mice
|
|
|
♀ | phenotype observed in females |
♂ | phenotype observed in males |
N | normal phenotype |
• most mice only survive 3 weeks before dying of widespread inflammation
|
• most mice die between E8.5 and E12.5
|
• in non-viable mice
|
• rarely
|
• in non-viable mice
|
• rarely
|
Mouse Genome Database (MGD), Gene Expression Database (GXD), Mouse Models of Human Cancer database (MMHCdb) (formerly Mouse Tumor Biology (MTB)), Gene Ontology (GO) |
||
Citing These Resources Funding Information Warranty Disclaimer, Privacy Notice, Licensing, & Copyright Send questions and comments to User Support. |
last database update 12/17/2024 MGI 6.24 |
|
|