About   Help   FAQ
Phenotypes associated with this allele
Allele Symbol
Allele Name
Allele ID
Tg(C3-1-TAg)cJeg
transgene insertion c, Jeffrey E Green
MGI:3039067
Summary 3 genotypes
Jump to Allelic Composition Genetic Background Genotype ID
cx1
Prlrtm1Cnp/Prlrtm1Cnp
Tg(C3-1-TAg)cJeg/0
involves: 129P2/OlaHsd * 129S2/SvPas * FVB/N MGI:4431014
tg2
Tg(C3-1-TAg)cJeg/0 FVB/N-Tg(C3-1-TAg)cJeg MGI:4431013
tg3
Tg(C3-1-TAg)cJeg/0 involves: FVB/N MGI:3835423


Genotype
MGI:4431014
cx1
Allelic
Composition
Prlrtm1Cnp/Prlrtm1Cnp
Tg(C3-1-TAg)cJeg/0
Genetic
Background
involves: 129P2/OlaHsd * 129S2/SvPas * FVB/N
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Prlrtm1Cnp mutation (2 available); any Prlr mutation (45 available)
Tg(C3-1-TAg)cJeg mutation (2 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
neoplasm
• mice exhibit a decrease in prostate intraepithelial neoplasia (PIN) in the ventral lobe compared with Tg(C3-1-TAg)cJeg mice
• however, PIN development in the dorsal lobe is the same as in Tg(C3-1-TAg)cJeg mice and mice do not develop prostate tumors

endocrine/exocrine glands
• mice exhibit a decrease in prostate intraepithelial neoplasia (PIN) in the ventral lobe compared with Tg(C3-1-TAg)cJeg mice
• however, PIN development in the dorsal lobe is the same as in Tg(C3-1-TAg)cJeg mice and mice do not develop prostate tumors

reproductive system
• mice exhibit a decrease in prostate intraepithelial neoplasia (PIN) in the ventral lobe compared with Tg(C3-1-TAg)cJeg mice
• however, PIN development in the dorsal lobe is the same as in Tg(C3-1-TAg)cJeg mice and mice do not develop prostate tumors




Genotype
MGI:4431013
tg2
Allelic
Composition
Tg(C3-1-TAg)cJeg/0
Genetic
Background
FVB/N-Tg(C3-1-TAg)cJeg
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Tg(C3-1-TAg)cJeg mutation (2 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
neoplasm
• mice develop prostate intraepithelial neoplasia (PIN) unlike wild-type mice
• PIN is higher in the ventral lobe compared to in the dorsal lobe

endocrine/exocrine glands
• mice develop prostate intraepithelial neoplasia (PIN) unlike wild-type mice
• PIN is higher in the ventral lobe compared to in the dorsal lobe

reproductive system
• mice develop prostate intraepithelial neoplasia (PIN) unlike wild-type mice
• PIN is higher in the ventral lobe compared to in the dorsal lobe




Genotype
MGI:3835423
tg3
Allelic
Composition
Tg(C3-1-TAg)cJeg/0
Genetic
Background
involves: FVB/N
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Tg(C3-1-TAg)cJeg mutation (2 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
neoplasm
• some mice exhibit mixed tumors of the sweat glands and occasional nasal proliferative or neoplastic lesions develop from the nasal turbinate epithelium unlike in wild-type mice
• by 6 months of age female mice develop multiple mammary ductular adenocarcinomas unlike in wild-type mice (J:46513)
• at 6 months, 10% of female mice exhibit lung metastasis (J:46513)
• adenocarcinoma cells exhibit increased rates of apoptosis compared to cells in wild-type mice (J:46513)
• adenocarcinomas are classified as Dunn type B tumors (J:52786)
• adenocarcinomas are classified as Dunn type B tumors nonporous females typically develop mammary adenocarcinoma at about 4 months of age while females that become pregnant show accelerated adenocarcinoma development (J:52786)
• at 7 months, 10% to 20% male mice develop adenocarcinomas of the bulbourethral glands unlike in wild-type mice
• at 7 months in the ventral prostate and 11 months in the dorsolateral prostate (J:46513)
• however, no metastasis is observed (J:46513)
(J:52786)
• at 7 months of age, 19% of mice exhibit carcinomas in the ventral lobe and 3% in the dorsolateral lobe unlike in wild-type mice (J:72324)
• after 8 months, 40% of mice exhibit carcinomas in the ventral lobe and 13% in the dorsolateral lobe unlike in wild-type mice (J:72324)
• the number of apoptotic cells in the prostate is greater than in wild-type mice (J:72324)
• at 2 to 3 months, low-grade prostate intraepithelial neoplasia (PIN) is observed in the ventral and dorsolateral prostates unlike in wild-type mice (J:46513)
• at 5 months, high-grade PIN is observed in both lobes unlike in wild-type mice (J:46513)
• PIN lesions increase with age (J:46513)
• at 5 to 6 months, mice develop low to high grade prostate intraepithelial neoplasia (PIN) unlike wild-type mice (J:72324)
• low-grade PIN is observed in 83% and 100% of the ventral prostate at 2 to 3 months and 4 to 12 months, respectively, unlike wild-type mice (J:72324)
• at 5 months, ventral and dorsolateral lobes exhibit high grade PIN unlike in wild-type mice (J:72324)
• high-grade PIN is observed on 88% and 100% of mice at 5 to 8 months and more than 8 months, respectively, unlike in wild-type mice (J:72324)
• numbers of PIN lesions increase with age in the ventral and dorsolateral lobes unlike wild-type mice (J:72324)
• the number of apoptotic cells in the prostate is greater than in wild-type mice (J:72324)
• at 7 months, 10% to 20% male mice develop adenocarcinomas of the urethral glands unlike in wild-type mice

endocrine/exocrine glands
• 2/3 of females develop atypical hyperplasia in the ducts and acini of mammary glands by 3 months of age
• 2/3 of females develop atypical hyperplasia in the ducts and acini of mammary glands by 3 months of age
• acini lesions resemble hyperplastic alveolar nodules
• by 6 months of age female mice develop multiple mammary ductular adenocarcinomas unlike in wild-type mice (J:46513)
• at 6 months, 10% of female mice exhibit lung metastasis (J:46513)
• adenocarcinoma cells exhibit increased rates of apoptosis compared to cells in wild-type mice (J:46513)
• adenocarcinomas are classified as Dunn type B tumors (J:52786)
• adenocarcinomas are classified as Dunn type B tumors nonporous females typically develop mammary adenocarcinoma at about 4 months of age while females that become pregnant show accelerated adenocarcinoma development (J:52786)
• at 2 months of age, female mice exhibit atypical ductal hyperplasias unlike in wild-type mice
• hyperplastic cells exhibit increased rates of apoptosis compared to cells in wild-type mice
• hyperplastic changes in the epithelium of the dorsal/ventral regions of the prostate are seen as early as 3 months of age
• at 7 months, 10% to 20% male mice develop adenocarcinomas of the bulbourethral glands unlike in wild-type mice
• at 7 months in the ventral prostate and 11 months in the dorsolateral prostate (J:46513)
• however, no metastasis is observed (J:46513)
(J:52786)
• at 7 months of age, 19% of mice exhibit carcinomas in the ventral lobe and 3% in the dorsolateral lobe unlike in wild-type mice (J:72324)
• after 8 months, 40% of mice exhibit carcinomas in the ventral lobe and 13% in the dorsolateral lobe unlike in wild-type mice (J:72324)
• the number of apoptotic cells in the prostate is greater than in wild-type mice (J:72324)
• at 2 to 3 months, low-grade prostate intraepithelial neoplasia (PIN) is observed in the ventral and dorsolateral prostates unlike in wild-type mice (J:46513)
• at 5 months, high-grade PIN is observed in both lobes unlike in wild-type mice (J:46513)
• PIN lesions increase with age (J:46513)
• at 5 to 6 months, mice develop low to high grade prostate intraepithelial neoplasia (PIN) unlike wild-type mice (J:72324)
• low-grade PIN is observed in 83% and 100% of the ventral prostate at 2 to 3 months and 4 to 12 months, respectively, unlike wild-type mice (J:72324)
• at 5 months, ventral and dorsolateral lobes exhibit high grade PIN unlike in wild-type mice (J:72324)
• high-grade PIN is observed on 88% and 100% of mice at 5 to 8 months and more than 8 months, respectively, unlike in wild-type mice (J:72324)
• numbers of PIN lesions increase with age in the ventral and dorsolateral lobes unlike wild-type mice (J:72324)
• the number of apoptotic cells in the prostate is greater than in wild-type mice (J:72324)
• prostate cells exhibit increased proliferation and apoptosis rates compared to in wild-type mice according to their degree of prostate intraepithelial neoplasia

reproductive system
• hyperplastic changes in the epithelium of the dorsal/ventral regions of the prostate are seen as early as 3 months of age
• at 7 months in the ventral prostate and 11 months in the dorsolateral prostate (J:46513)
• however, no metastasis is observed (J:46513)
(J:52786)
• at 7 months of age, 19% of mice exhibit carcinomas in the ventral lobe and 3% in the dorsolateral lobe unlike in wild-type mice (J:72324)
• after 8 months, 40% of mice exhibit carcinomas in the ventral lobe and 13% in the dorsolateral lobe unlike in wild-type mice (J:72324)
• the number of apoptotic cells in the prostate is greater than in wild-type mice (J:72324)
• at 2 to 3 months, low-grade prostate intraepithelial neoplasia (PIN) is observed in the ventral and dorsolateral prostates unlike in wild-type mice (J:46513)
• at 5 months, high-grade PIN is observed in both lobes unlike in wild-type mice (J:46513)
• PIN lesions increase with age (J:46513)
• at 5 to 6 months, mice develop low to high grade prostate intraepithelial neoplasia (PIN) unlike wild-type mice (J:72324)
• low-grade PIN is observed in 83% and 100% of the ventral prostate at 2 to 3 months and 4 to 12 months, respectively, unlike wild-type mice (J:72324)
• at 5 months, ventral and dorsolateral lobes exhibit high grade PIN unlike in wild-type mice (J:72324)
• high-grade PIN is observed on 88% and 100% of mice at 5 to 8 months and more than 8 months, respectively, unlike in wild-type mice (J:72324)
• numbers of PIN lesions increase with age in the ventral and dorsolateral lobes unlike wild-type mice (J:72324)
• the number of apoptotic cells in the prostate is greater than in wild-type mice (J:72324)
• prostate cells exhibit increased proliferation and apoptosis rates compared to in wild-type mice according to their degree of prostate intraepithelial neoplasia

integument
• 2/3 of females develop atypical hyperplasia in the ducts and acini of mammary glands by 3 months of age
• 2/3 of females develop atypical hyperplasia in the ducts and acini of mammary glands by 3 months of age
• acini lesions resemble hyperplastic alveolar nodules
• by 6 months of age female mice develop multiple mammary ductular adenocarcinomas unlike in wild-type mice (J:46513)
• at 6 months, 10% of female mice exhibit lung metastasis (J:46513)
• adenocarcinoma cells exhibit increased rates of apoptosis compared to cells in wild-type mice (J:46513)
• adenocarcinomas are classified as Dunn type B tumors (J:52786)
• adenocarcinomas are classified as Dunn type B tumors nonporous females typically develop mammary adenocarcinoma at about 4 months of age while females that become pregnant show accelerated adenocarcinoma development (J:52786)
• at 2 months of age, female mice exhibit atypical ductal hyperplasias unlike in wild-type mice
• hyperplastic cells exhibit increased rates of apoptosis compared to cells in wild-type mice

mortality/aging
• survival of males is longer than females, with 50% survival at around 4 months of age for females and 8 months of age for males
• all females die by 5-6 months of age, while all males die by 11 months of age

renal/urinary system
• at 7 months, 10% to 20% male mice develop adenocarcinomas of the bulbourethral glands unlike in wild-type mice
• at 7 months, 10% to 20% male mice develop adenocarcinomas of the urethral glands unlike in wild-type 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)
Citing These Resources
Funding Information
Warranty Disclaimer, Privacy Notice, Licensing, & Copyright
Send questions and comments to User Support.
last database update
04/16/2024
MGI 6.23
The Jackson Laboratory