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Phenotypes Associated with This Genotype
Genotype
MGI:4442799
Allelic
Composition
Trp73tm2Mak/Trp73tm2Mak
Genetic
Background
either: B6.129P2-Trp73tm2Mak or (involves: 129P2/OlaHsd * C57BL/6J)
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Trp73tm2Mak mutation (3 available); any Trp73 mutation (47 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
mortality/aging
• the sex ratio was slightly but significantly skewed at birth with fewer females being born than males

nervous system
• neuronal density is significantly reduced in the motor cortex at 10 and 26-27 months of age
• by 26-27 mo of age, motor cortex thickness is reduced significantly
• neuronal density is significantly reduced in the motor cortex at 10 and 26-27 months of age
• signs of mild neurodegeneration are seen such as an increase in the number of condensed cells at 10 months of age

hematopoietic system
• increased apoptosis in response to DNA damaging agents (cisplatin, doxorubicin, etoposide and gamma-irradiation)

immune system
• increased apoptosis in response to DNA damaging agents (cisplatin, doxorubicin, etoposide and gamma-irradiation)

homeostasis/metabolism
• both MEFs and thymocytes show increased sensitivity to gamma irradiation induced apoptosis
• both MEFs and thymocytes show increased sensitivity to DNA damaging agents including, cisplatin, doxorubicin and etoposide

cellular
• both MEFs and thymocytes show increased sensitivity to DNA damaging agents including, cisplatin, doxorubicin and etoposide
• however, no difference in the apoptotic response to UV treatment, TNFalpha treatment, or IL-2 withdrawal is detected
• both MEFs and thymocytes show increased sensitivity to gamma irradiation induced apoptosis
• increased apoptosis in response to DNA damaging agents (cisplatin, doxorubicin, etoposide and gamma-irradiation)

endocrine/exocrine glands
• increased apoptosis in response to DNA damaging agents (cisplatin, doxorubicin, etoposide and gamma-irradiation)


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
01/06/2026
MGI 6.24
The Jackson Laboratory