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Phenotypes associated with this allele
Allele Symbol
Allele Name
Allele ID
Gt(ROSA)26Sortm1(tTA,tetO-Mir21)Fjsl
targeted mutation 1, Frank J Slack
MGI:4830734
Summary 1 genotype
Jump to Allelic Composition Genetic Background Genotype ID
cn1
Gt(ROSA)26Sortm1(tTA,tetO-Mir21)Fjsl/Gt(ROSA)26Sor+
Tg(Nes-cre)1Wmz/0
involves: C57BL/6 * C57BL/6J * SJL/J MGI:4830769


Genotype
MGI:4830769
cn1
Allelic
Composition
Gt(ROSA)26Sortm1(tTA,tetO-Mir21)Fjsl/Gt(ROSA)26Sor+
Tg(Nes-cre)1Wmz/0
Genetic
Background
involves: C57BL/6 * C57BL/6J * SJL/J
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Gt(ROSA)26Sortm1(tTA,tetO-Mir21)Fjsl mutation (0 available); any Gt(ROSA)26Sor mutation (944 available)
Tg(Nes-cre)1Wmz mutation (0 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
growth/size/body
• 8-fold in severe cases after doxycycline withdrawal

mortality/aging
• mice not fed doxycycline exhibit die before 3 months of age unlike wild-type mice
• however, mice fed doxycycline are alive at 3 months of age

immune system
• after doxycycline withdrawal, thymus structure is altered by invasion of neoplastic cells unlike in similarly treated wild-type mice
• 20-fold in severe cases after doxycycline withdrawal
• in 4 of 7 mice at 3 months
• after doxycycline withdrawal, spleen abnormalities are due to malignant invasion of red pulp unlike in similarly treated wild-type mice
• 8-fold in severe cases after doxycycline withdrawal
• after doxycycline withdrawal
• two months after doxycycline withdrawal and in mice not fed doxycycline

neoplasm
• mice fed doxycycline after a period of not consuming it exhibit regression of lymphomas associated with increased apoptosis of tumor cells and decreased cell proliferation compared with untreated mice
• after doxycycline withdrawal, mice exhibit malignant invasion in the spleen, thymus, peripheral blood, and other organs, especially the liver and less frequently the kidney, unlike in similarly treated wild-type mice
• however, mice fed doxycycline exhibit remission of tumors and tumor-associated pathologies
• mice not fed doxycycline exhibit external signs of lymphoma (lymphadenopathy and/or paresis of rear limbs) unlike wild-type mice
• however, mice fed doxycycline do not exhibit pathologies associated with lymphomas

behavior/neurological
• two months after doxycycline withdrawal
• paresis in the hindlimbs two months after doxycycline withdrawal

skeleton
• after doxycycline withdrawal, mice exhibit extended bone marrow in the thoracic and lumbar vertebrae, femur, sternum, and hard palate causing paresis, bone fractures, and invasion of surrounding tissue unlike similarly treated wild-type mice

respiratory system
• two months after doxycycline withdrawal

hematopoietic system
• after doxycycline withdrawal, thymus structure is altered by invasion of neoplastic cells unlike in similarly treated wild-type mice
• 20-fold in severe cases after doxycycline withdrawal
• at 3 months
• however, mice treated with doxycyline do not exhibit anemia
• in 4 of 7 mice at 3 months
• after doxycycline withdrawal, spleen abnormalities are due to malignant invasion of red pulp unlike in similarly treated wild-type mice
• 8-fold in severe cases after doxycycline withdrawal
• after doxycycline withdrawal

integument
• two months after doxycycline withdrawal

endocrine/exocrine glands
• after doxycycline withdrawal, thymus structure is altered by invasion of neoplastic cells unlike in similarly treated wild-type mice
• 20-fold in severe cases after doxycycline withdrawal





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last database update
04/30/2024
MGI 6.23
The Jackson Laboratory