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Phenotypes Associated with This Genotype
Genotype
MGI:5502351
Allelic
Composition
Nabp2tm1.1Kkha/Nabp2tm1.1Kkha
Gt(ROSA)26Sortm9(cre/ESR1)Arte/Gt(ROSA)26Sor+
Genetic
Background
involves: C57BL/6 * C57BL/6NTac
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Gt(ROSA)26Sortm9(cre/ESR1)Arte mutation (2 available); any Gt(ROSA)26Sor mutation (997 available)
Nabp2tm1.1Kkha mutation (1 available); any Nabp2 mutation (16 available)
phenotype observed in females
phenotype observed in males
N normal phenotype

Testicular degeneration in Nabp2tm1.1Kkha/Nabp2tm1.1Kkha Gt(ROSA)26Sortm9(cre/ESR1)Arte/Gt(ROSA)26Sor+ mice

mortality/aging

reproductive system
N
• tamoxifen-treated female mice exhibit normal fertility
• premature sloughing from the supporting Sertoli cells in tamoxifen-treated mice
• due to apoptosis and premature sloughing from the supporting Sertoli cells in tamoxifen-treated mice
• decreased elongated spermatids
• in tamoxifen-treated mice
• in tamoxifen-treated mice
• in tamoxifen-treated mice
• bilateral degeneration; tubules showed degenerate, sometimes vacuolated, or necrotic spermatogenic cells, the latter with pyknotic nuclei and hypereosinophilic cytoplasm, or apoptotic body formation in tamoxifen-treated mice
• from tamoxifen-treated mice with longer intervals between litters
• in tamoxifen-treated mice

neoplasm
• splenic and metastatic B lymphomas, T cell lymphoma in thymus, hepatocellular carcinoma and B or T lymphoblastic leukemia in 11 of 35 of tamoxifen-treated mice
• in thymus of some tamoxifen-treated mice
• in some tamoxifen-treated mice
• B or T lymphoblastic leukemia in some tamoxifen-treated mice
• splenic and metastatic B lymphomas in some tamoxifen-treated mice

cellular
• premature sloughing from the supporting Sertoli cells in tamoxifen-treated mice
• due to apoptosis and premature sloughing from the supporting Sertoli cells in tamoxifen-treated mice
• decreased elongated spermatids
• tamoxifen-treated mice exposed to ionizing radiation exhibit distended crypt lumina lined by attenuated enterocytes, desquamated necrotic cellular debris and a small increase of cells near deep crypts with apoptotic bodies
• however, blood counts are normal in irradiated tamoxifen-treated mice
• in irradiated tamoxifen-treated mice
• in tamoxifen-treated mice
• in tamoxifen-treated mice

growth/size/body
• at E14.5 and E18.5

digestive/alimentary system
• tamoxifen-treated mice exposed to ionizing radiation exhibit distended crypt lumina lined by attenuated enterocytes, desquamated necrotic cellular debris and a small increase of cells near deep crypts with apoptotic bodies

immune system
• in irradiated tamoxifen-treated mice

endocrine/exocrine glands
• in irradiated tamoxifen-treated mice
• in tamoxifen-treated mice
• in tamoxifen-treated mice
• bilateral degeneration; tubules showed degenerate, sometimes vacuolated, or necrotic spermatogenic cells, the latter with pyknotic nuclei and hypereosinophilic cytoplasm, or apoptotic body formation in tamoxifen-treated mice
• in thymus of some tamoxifen-treated mice

hematopoietic system
N
• blood counts are normal in irradiated tamoxifen-treated mice
• in irradiated tamoxifen-treated mice

homeostasis/metabolism

liver/biliary system
• in some tamoxifen-treated mice


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
09/17/2024
MGI 6.24
The Jackson Laboratory