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Phenotypes Associated with This Genotype
Genotype
MGI:5790497
Allelic
Composition
Ctnnb1tm1Mmt/Ctnnb1tm1Mmt
Tg(Upk2-cre)6Xrw/0
Tg(Upk2-HRAS*Q61L)5Xrw/0
Genetic
Background
involves: 129X1/SvJ * FVB/N
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Ctnnb1tm1Mmt mutation (0 available); any Ctnnb1 mutation (49 available)
Tg(Upk2-cre)6Xrw mutation (0 available)
Tg(Upk2-HRAS*Q61L)5Xrw mutation (0 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
mortality/aging
• mean survival of 231 days and median survival of 236 days

neoplasm
• mice rapidly develop bladder tumors with progression to non-invasive papillary carcinomas (urothelial cell carcinoma)
• the number of proliferating cells within each tumor is increased compared to single conditional Ctnnb1tm1Mmt homozygotes
• mice treated with a MEK1/2 inhibitor, PD184352, show tumor regression and reduction in proliferation

renal/urinary system
• due to bladder tumors
• mice rapidly develop bladder tumors with progression to non-invasive papillary carcinomas (urothelial cell carcinoma)
• the number of proliferating cells within each tumor is increased compared to single conditional Ctnnb1tm1Mmt homozygotes
• mice treated with a MEK1/2 inhibitor, PD184352, show tumor regression and reduction in proliferation

homeostasis/metabolism
• due to bladder tumors

Mouse Models of Human Disease
DO ID OMIM ID(s) Ref(s)
urinary bladder cancer DOID:11054 OMIM:109800
J:234236


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
04/16/2024
MGI 6.23
The Jackson Laboratory