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Phenotypes associated with this allele
Allele Symbol
Allele Name
Allele ID
Igs2tm1(CAG-Met)Zsu
targeted mutation 1, Zijie Sun
MGI:6507851
Summary 3 genotypes
Jump to Allelic Composition Genetic Background Genotype ID
cn1
Igs2tm1(CAG-Met)Zsu/Igs2+
Ptentm1Hwu/Ptentm1Hwu
Tg(Pbsn-cre)4Prb/0
involves: 129 * C57BL/6 * DBA/2 * FVB/N MGI:6507866
cn2
Igs2tm1(CAG-Met)Zsu/Igs2+
Tg(Pbsn-cre)4Prb/0
involves: 129S1/Sv * 129X1/SvJ * C57BL/6 * DBA/2 * FVB/N MGI:6507865
cn3
Ctnnb1tm1Mmt/Ctnnb1+
Igs2tm1(CAG-Met)Zsu/Igs2+
Tg(Pbsn-cre)4Prb/0
involves: 129S1/Sv * 129X1/SvJ * C57BL/6 * DBA/2 * FVB/N MGI:6507888


Genotype
MGI:6507866
cn1
Allelic
Composition
Igs2tm1(CAG-Met)Zsu/Igs2+
Ptentm1Hwu/Ptentm1Hwu
Tg(Pbsn-cre)4Prb/0
Genetic
Background
involves: 129 * C57BL/6 * DBA/2 * FVB/N
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Igs2tm1(CAG-Met)Zsu mutation (0 available); any Igs2 mutation (68 available)
Ptentm1Hwu mutation (16 available); any Pten mutation (81 available)
Tg(Pbsn-cre)4Prb mutation (2 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
endocrine/exocrine glands
• mice develop prostatic sarcomatoid carcinoma
• mice show a more aggressive prostatic tumor phenotype than single conditional Ptentm1Hwu mice
• mice develop prostatic adenocarcinomas and invasive carcinomas
• 5 of 5 mice develop multifocal high grade intraepithelial neoplasia (PIN) before 4 months of age

neoplasm
• mice develop prostatic sarcomatoid carcinoma
• mice show a more aggressive prostatic tumor phenotype than single conditional Ptentm1Hwu mice
• mice develop prostatic adenocarcinomas and invasive carcinomas
• 5 of 5 mice develop multifocal high grade intraepithelial neoplasia (PIN) before 4 months of age
• prostate cancer metastasis after 10 months of age with 62.5% of mice showing metastatic lesions
• metastasis to lungs and periprostatic lymph nodes is seen
• mice show an overall more invasive tumor phenotype than single conditional Ptentm1Hwu mice
• 1 of 5 mice show invasive pancreatic carcinoma at 4-10 months and 6 of 8 mice develop invasive carcinoma after 10 months of age; 5 of 8 mice have invasive carcinoma with epithelial-mesenchymal transition and 5 of 8 mice have invasive carcinoma with metastasis
• mice exhibit a transition from prostatic adenocarcinoma and invasive carcinoma lesions to pathology resembling prostatic sarcamoid carcinomas
• sarcamoid carcinomas show spindle-like tumor cells, tumor cells with a multitude of mitotic figures, and haphazard acini and lobules of pleomorphic cells, indicating that these lesions possess mesenchymal morphology and proliferative and invasive features

reproductive system
• mice develop prostatic sarcomatoid carcinoma
• mice show a more aggressive prostatic tumor phenotype than single conditional Ptentm1Hwu mice
• mice develop prostatic adenocarcinomas and invasive carcinomas
• 5 of 5 mice develop multifocal high grade intraepithelial neoplasia (PIN) before 4 months of age




Genotype
MGI:6507865
cn2
Allelic
Composition
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:
Igs2tm1(CAG-Met)Zsu mutation (0 available); any Igs2 mutation (68 available)
Tg(Pbsn-cre)4Prb mutation (2 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
endocrine/exocrine glands
N
• mice do not show any obvious pathological changes in prostate tissues from birth to 20 months of age
• mice administered recombinant human hepatocyte growth factor at 6 months of age show lesions of typical low-grade prostatic intraepithelial neoplasia not seen in hepatocyte growth factor-administered wild-type mice
• however, hepatocyte growth factor-administered mice do not develop prostate carcinomas

reproductive system
• mice administered recombinant human hepatocyte growth factor at 6 months of age show lesions of typical low-grade prostatic intraepithelial neoplasia not seen in hepatocyte growth factor-administered wild-type mice
• however, hepatocyte growth factor-administered mice do not develop prostate carcinomas

neoplasm
• mice administered recombinant human hepatocyte growth factor at 6 months of age show lesions of typical low-grade prostatic intraepithelial neoplasia not seen in hepatocyte growth factor-administered wild-type mice
• however, hepatocyte growth factor-administered mice do not develop prostate carcinomas




Genotype
MGI:6507888
cn3
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 (68 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





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last database update
05/21/2024
MGI 6.23
The Jackson Laboratory