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Phenotypes Associated with This Genotype
Genotype
MGI:2174779
Allelic
Composition
Trp53tm1Brd/Trp53tm1Brd
Genetic
Background
involves: 129S7/SvEvBrd * C57BL/6
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Trp53tm1Brd mutation (5 available); any Trp53 mutation (232 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
mortality/aging
• 6 of 35 die from unknown causes, with no tumors (J:1999)
• mice succumb to tumorigenesis by 8 months of age (J:126497)

neoplasm
• 26 of 35 (76%) develop a variety of neoplasms by 6 months of age (J:1999)
• tumor occurrence increases rapidly between 15 and 25 weeks of age (J:1999)
• spontaneously develop fatal tumors by 10 months of age (J:108183)
• most frequent tumors observed are malignant lymphomas that involve the thymus and other major visceral organs
• sarcomas are also frequently observed and include hemangiosarcoma, undifferentiated sarcomas and osteosarcoma (J:1999)
• in 8 of 26 mice (J:126497)

cellular
• the G2 to M check point is impaired after irradiation of mouse embryonic fibroblasts
• MEFs sensitized to apoptosis by E1A overexpression show very low levels of apoptosis induced by irradiation or chemical treatment compared to wild-type or Trp53tm1Wahl MEFs (J:108183)
• p53-dependent apoptosis following exposure to radiation is abolished (J:126497)
• E12.5 primary telencephalic cultures show resistance to AraC induced caspase 3 activation and neuronal cell death

nervous system
• E12.5 primary telencephalic cultures show resistance to AraC induced caspase 3 activation and neuronal cell death

skeleton

endocrine/exocrine glands


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
04/23/2024
MGI 6.23
The Jackson Laboratory