Phenotypes associated with this allele
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Find Mice |
Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Trp53tm1.1Brn mutation
(0 available);
any
Trp53 mutation
(232 available)
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neoplasm
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• mice exhibit a similar increase in tumor incidence with the same spectrum as in other Trp53 null mice
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• median tumor-free survival is 116 days compared to 515 in heterozygotes
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Find Mice |
Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Trp53tm1.1Brn mutation
(0 available);
any
Trp53 mutation
(232 available)
Trp53tm1Brn mutation
(18 available);
any
Trp53 mutation
(232 available)
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neoplasm
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• in all mice treated with a cre-expressing adenovirus
(J:86077)
• in 6 of 7 mice following treatment with cre-expressing adenovirus
(J:157319)
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respiratory system
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• in all mice treated with a cre-expressing adenovirus
(J:86077)
• in 6 of 7 mice following treatment with cre-expressing adenovirus
(J:157319)
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|
Find Mice |
Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Tg(KRT14-cre)8Brn mutation
(4 available)
Trp53tm1.1Brn mutation
(0 available);
any
Trp53 mutation
(232 available)
Trp53tm3Tyj mutation
(3 available);
any
Trp53 mutation
(232 available)
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neoplasm
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• skin tumors develop between 200 and 300 days
• whether spontaneous or induced, mice develop epithelial, proliferative lesions forming a continuum from nonneoplastic squamous keratosis and acanthosis to squamous cell papillomas, actinic keratosis and keratoacanthoma with increasing degrees of atypia and dysplasia, carcinoma in situ, up to invasive squamous cell carcinoma
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cellular
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• fewer CASP3+ cells area found following UVB treatment when compared to wild-type mice
• the reduction in apoptotic cells is slightly greater in homozygotes than in heterozygotes
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integument
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• skin tumors develop between 200 and 300 days
• whether spontaneous or induced, mice develop epithelial, proliferative lesions forming a continuum from nonneoplastic squamous keratosis and acanthosis to squamous cell papillomas, actinic keratosis and keratoacanthoma with increasing degrees of atypia and dysplasia, carcinoma in situ, up to invasive squamous cell carcinoma
|
|
Find Mice |
Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Tg(KRT14-cre)8Brn mutation
(4 available)
Trp53tm1.1Brn mutation
(0 available);
any
Trp53 mutation
(232 available)
|
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neoplasm
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• skin tumors develop between 500 and 600 days
• UVB exposure results in 2.4+/-0.6 tumors at day 100 compared to 6.5+/-1.4 in Trp53tm3Tyj Tg(KRT14-cre)8Brn heterozygotes and 0.6+/-0.2 in wild-type mice
• whether spontaneous or induced, mice develop epithelial, proliferative lesions forming a continuum from nonneoplastic squamous keratosis and acanthosis to squamous cell papillomas, actinic keratosis and keratoacanthoma with increasing degrees of atypia and dysplasia, carcinoma in situ, up to invasive squamous cell carcinoma
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cellular
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• fewer CASP3+ cells area found following UVB treatment when compared to wild-type mice
• the reduction in apoptotic cells is slightly greater in homozygotes than in heterozygotes
|
integument
|
• skin tumors develop between 500 and 600 days
• UVB exposure results in 2.4+/-0.6 tumors at day 100 compared to 6.5+/-1.4 in Trp53tm3Tyj Tg(KRT14-cre)8Brn heterozygotes and 0.6+/-0.2 in wild-type mice
• whether spontaneous or induced, mice develop epithelial, proliferative lesions forming a continuum from nonneoplastic squamous keratosis and acanthosis to squamous cell papillomas, actinic keratosis and keratoacanthoma with increasing degrees of atypia and dysplasia, carcinoma in situ, up to invasive squamous cell carcinoma
|
|
Find Mice |
Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Tg(KRT14-cre)8Brn mutation
(4 available)
Trp53tm1.1Brn mutation
(0 available);
any
Trp53 mutation
(232 available)
|
|
|
neoplasm
|
• skin tumors develop between 200 and 300 days
• whether spontaneous or induced, mice develop epithelial, proliferative lesions forming a continuum from nonneoplastic squamous keratosis and acanthosis to squamous cell papillomas, actinic keratosis and keratoacanthoma with increasing degrees of atypia and dysplasia, carcinoma in situ, up to invasive squamous cell carcinoma
|
cellular
|
• fewer CASP3+ cells area found following UVB treatment when compared to wild-type mice
• the reduction in apoptotic cells is slightly greater in homozygotes than in heterozygotes
|
integument
|
• skin tumors develop between 200 and 300 days
• whether spontaneous or induced, mice develop epithelial, proliferative lesions forming a continuum from nonneoplastic squamous keratosis and acanthosis to squamous cell papillomas, actinic keratosis and keratoacanthoma with increasing degrees of atypia and dysplasia, carcinoma in situ, up to invasive squamous cell carcinoma
|
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Find Mice |
Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Atmintm1.1Jhh mutation
(2 available);
any
Atmin mutation
(38 available)
Trp53tm1.1Brn mutation
(0 available);
any
Trp53 mutation
(232 available)
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mortality/aging
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• no mice are present at weaning
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