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Phenotypes Associated with This Genotype
Genotype
MGI:6507888
Allelic
Composition
Ctnnb1tm1Mmt/Ctnnb1+
Igs2tm1(CAG-Met)Zsu/Igs2+
Tg(Pbsn-cre)4Prb/0
Genetic
Background
involves: 129S1/Sv * 129X1/SvJ * C57BL/6 * DBA/2 * FVB/N
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Ctnnb1tm1Mmt mutation (0 available); any Ctnnb1 mutation (49 available)
Igs2tm1(CAG-Met)Zsu mutation (0 available); any Igs2 mutation (72 available)
Tg(Pbsn-cre)4Prb mutation (2 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
endocrine/exocrine glands
• mice develop aggressive adenocarcinomas that occur with much higher frequency than in single Ctnnb1tm1Mmt conditional mutants, developing prostatic invasive adenocarcinomas as early as 7 months of age
• 4 of 4 mice show intracystic adenocarcinoma at 6-9 months of age, with 1 of 4 mice showing invasive adenocarcinoma
• 13 of 13 mice show intracystic adenocarcinoma at 9 months or older, with 5 of 13 showing invasive adenocarcinoma
• mice develop PIN lesions starting at 4-6 weeks of age, with 5 of 5 mice showing high grade PIN before 6 months of age
• mice develop more severe PIN lesions and faster disease progression than single Ctnnb1tm1Mmt conditional mutants
• lesions in the anterior, dorsal, and lateral prostate lobes are more severe than in the ventral prostate
• typical cribriform and papilliferous structures completely fill the lumen of prostatic glands

neoplasm
• mice develop aggressive adenocarcinomas that occur with much higher frequency than in single Ctnnb1tm1Mmt conditional mutants, developing prostatic invasive adenocarcinomas as early as 7 months of age
• 4 of 4 mice show intracystic adenocarcinoma at 6-9 months of age, with 1 of 4 mice showing invasive adenocarcinoma
• 13 of 13 mice show intracystic adenocarcinoma at 9 months or older, with 5 of 13 showing invasive adenocarcinoma
• mice develop PIN lesions starting at 4-6 weeks of age, with 5 of 5 mice showing high grade PIN before 6 months of age
• mice develop more severe PIN lesions and faster disease progression than single Ctnnb1tm1Mmt conditional mutants
• lesions in the anterior, dorsal, and lateral prostate lobes are more severe than in the ventral prostate
• typical cribriform and papilliferous structures completely fill the lumen of prostatic glands

reproductive system
• mice develop aggressive adenocarcinomas that occur with much higher frequency than in single Ctnnb1tm1Mmt conditional mutants, developing prostatic invasive adenocarcinomas as early as 7 months of age
• 4 of 4 mice show intracystic adenocarcinoma at 6-9 months of age, with 1 of 4 mice showing invasive adenocarcinoma
• 13 of 13 mice show intracystic adenocarcinoma at 9 months or older, with 5 of 13 showing invasive adenocarcinoma
• mice develop PIN lesions starting at 4-6 weeks of age, with 5 of 5 mice showing high grade PIN before 6 months of age
• mice develop more severe PIN lesions and faster disease progression than single Ctnnb1tm1Mmt conditional mutants
• lesions in the anterior, dorsal, and lateral prostate lobes are more severe than in the ventral prostate
• typical cribriform and papilliferous structures completely fill the lumen of prostatic 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
11/05/2024
MGI 6.24
The Jackson Laboratory