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Phenotypes associated with this allele
Allele Symbol
Allele Name
Allele ID
Tg(MMTV-Erbb2)1Pv
transgene insertion 1, Paolo Vezzoni
MGI:3039042
Summary 3 genotypes
Jump to Allelic Composition Genetic Background Genotype ID
cn1
Map2k7tm1.1Twad/Map2k7tm1.2Twad
Tg(MMTV-cre)4Mam/0
Tg(MMTV-Erbb2)1Pv/0
involves: 129P2/OlaHsd * C57BL/6 * CD-1 * DBA * FVB/N MGI:4948967
cx2
Stat3tm4Vpo/Stat3tm4Vpo
Tg(MMTV-Erbb2)1Pv/0
involves: 129P2/OlaHsd * BALB/cAn * C57BL/6 * CD-1 * DBA MGI:4438062
tg3
Tg(MMTV-Erbb2)1Pv/0 involves: BALB/c * C57BL/6 * CD-1 * DBA MGI:5796560


Genotype
MGI:4948967
cn1
Allelic
Composition
Map2k7tm1.1Twad/Map2k7tm1.2Twad
Tg(MMTV-cre)4Mam/0
Tg(MMTV-Erbb2)1Pv/0
Genetic
Background
involves: 129P2/OlaHsd * C57BL/6 * CD-1 * DBA * FVB/N
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Map2k7tm1.1Twad mutation (0 available); any Map2k7 mutation (19 available)
Map2k7tm1.2Twad mutation (0 available); any Map2k7 mutation (19 available)
Tg(MMTV-cre)4Mam mutation (1 available)
Tg(MMTV-Erbb2)1Pv mutation (0 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
mortality/aging
• compared with control mice

neoplasm
• mammary gland tumor onset is earlier and tumor burden heavier than in Tg(MMTV-Erbb2)1Pv mice

integument
• mammary gland tumor onset is earlier and tumor burden heavier than in Tg(MMTV-Erbb2)1Pv mice

endocrine/exocrine glands
• mammary gland tumor onset is earlier and tumor burden heavier than in Tg(MMTV-Erbb2)1Pv mice




Genotype
MGI:4438062
cx2
Allelic
Composition
Stat3tm4Vpo/Stat3tm4Vpo
Tg(MMTV-Erbb2)1Pv/0
Genetic
Background
involves: 129P2/OlaHsd * BALB/cAn * C57BL/6 * CD-1 * DBA
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Stat3tm4Vpo mutation (0 available); any Stat3 mutation (70 available)
Tg(MMTV-Erbb2)1Pv mutation (0 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
neoplasm
• mice develop palpable tumors significantly earlier than their littermate controls only carrying the transgene
• the presence of larger, more diffused and advanced neoplastic lesions in whole mount mammary gland preparations performed at 7, 12, and 17 weeks of age than their littermate controls only carrying the transgene
• normal proliferation rates in tumor lesions as assessed by PCNA staining
• invasive carcinomas at 12 weeks
• tumor cells group in solid masses with small aggregates invading the surrounding fibroadipose tissue
• only atypical hyperplastic foci and few in situ carcinomas in the littermate controls only carrying the transgene
• strongly enhanced Matrigel invasion potential in cell lines derived from tumors in mutant mice
• strongly enhanced metastatic potential, producing more and faster growing lung metastases both at 5 and 3 weeks when injected into nude mice
• produce tumors faster in nude mice, reaching a diameter of 10 mm 5 weeks after injection of the cell lines derived from tumors in mutant mice
• tumors produced by injection of the cell lines derived from tumors in transgene control mice grow much slower and never reach the 10-mm size

endocrine/exocrine glands
• mice develop palpable tumors significantly earlier than their littermate controls only carrying the transgene
• the presence of larger, more diffused and advanced neoplastic lesions in whole mount mammary gland preparations performed at 7, 12, and 17 weeks of age than their littermate controls only carrying the transgene
• normal proliferation rates in tumor lesions as assessed by PCNA staining
• invasive carcinomas at 12 weeks
• tumor cells group in solid masses with small aggregates invading the surrounding fibroadipose tissue
• only atypical hyperplastic foci and few in situ carcinomas in the littermate controls only carrying the transgene

cellular
• absence of cortical actin and presence of actin stress fibers in cell lines derived from tumors in mutant mice
• discontinuous E-cadherin, beta-catenin, and Zo-1 distribution in cell lines derived from tumors in mutant mice
• reduced TUNEL-positive apoptotic nuclei in tumor lesions
• increased migration (>2 fold) in cell lines derived from tumors in mutant mice

integument
• mice develop palpable tumors significantly earlier than their littermate controls only carrying the transgene
• the presence of larger, more diffused and advanced neoplastic lesions in whole mount mammary gland preparations performed at 7, 12, and 17 weeks of age than their littermate controls only carrying the transgene
• normal proliferation rates in tumor lesions as assessed by PCNA staining
• invasive carcinomas at 12 weeks
• tumor cells group in solid masses with small aggregates invading the surrounding fibroadipose tissue
• only atypical hyperplastic foci and few in situ carcinomas in the littermate controls only carrying the transgene




Genotype
MGI:5796560
tg3
Allelic
Composition
Tg(MMTV-Erbb2)1Pv/0
Genetic
Background
involves: BALB/c * C57BL/6 * CD-1 * DBA
Find Mice Using the International Mouse Strain Resource (IMSR)
No mouse lines available in IMSR.
See publication links below for author information.
phenotype observed in females
phenotype observed in males
N normal phenotype
neoplasm
• at 5-7 weeks of age, about 30% of mice exhibit mammary gland hyperplasia, from 8-13 weeks of age, 41% of mammary glands show atypical hyperplasia, features of carcinoma in situ are first seen at 14 weeks (9%) and progressively increase to 15% at 22-28 weeks, and invasive breast cancer (ductal breast adenocarcinoma) appears from week 22 and occupies 30% of the mammary glands
• microvessel density markedly increase with mammary gland tumor progression from simple to atypical hyperplasia

endocrine/exocrine glands
• at 5-7 weeks of age, about 30% of mice exhibit mammary gland hyperplasia, from 8-13 weeks of age, 41% of mammary glands show atypical hyperplasia, features of carcinoma in situ are first seen at 14 weeks (9%) and progressively increase to 15% at 22-28 weeks, and invasive breast cancer (ductal breast adenocarcinoma) appears from week 22 and occupies 30% of the mammary glands
• microvessel density markedly increase with mammary gland tumor progression from simple to atypical hyperplasia

integument
• at 5-7 weeks of age, about 30% of mice exhibit mammary gland hyperplasia, from 8-13 weeks of age, 41% of mammary glands show atypical hyperplasia, features of carcinoma in situ are first seen at 14 weeks (9%) and progressively increase to 15% at 22-28 weeks, and invasive breast cancer (ductal breast adenocarcinoma) appears from week 22 and occupies 30% of the mammary glands
• microvessel density markedly increase with mammary gland tumor progression from simple to atypical hyperplasia

Mouse Models of Human Disease
DO ID OMIM ID(s) Ref(s)
breast cancer DOID:1612 OMIM:114480
J:234420





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last database update
04/23/2024
MGI 6.23
The Jackson Laboratory