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Phenotypes associated with this allele
Allele Symbol
Allele Name
Allele ID
Tg(Ela1-TAg*)79Mjt
transgene insertion 79, Mary J Tevethia
MGI:3510407
Summary 2 genotypes
Jump to Allelic Composition Genetic Background Genotype ID
cx1
Tg(Ela1-TAg*)79Mjt/0
Tg(MUC1)79.24Gend/0
involves: C57BL/6 * DBA/2 MGI:3777635
tg2
Tg(Ela1-TAg*)79Mjt/0 involves: C57BL/6 * DBA/2 MGI:3777580


Genotype
MGI:3777635
cx1
Allelic
Composition
Tg(Ela1-TAg*)79Mjt/0
Tg(MUC1)79.24Gend/0
Genetic
Background
involves: C57BL/6 * DBA/2
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Tg(Ela1-TAg*)79Mjt mutation (0 available)
Tg(MUC1)79.24Gend mutation (1 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
neoplasm
• mice develop pancreatic tumors that can be grossly visualized at 9 weeks of age
• at 18 and 21 weeks, mice develop large solid tumor masses of less differentiated acinar cell carcinomas
• pancreas consists of acinar cell microadenomas
• pancreas consists of acinar cell carcinomas; well-differentiated acinar cell carcinomas are observed

endocrine/exocrine glands
• double transgenic mice exhibit acinar cell dysplasia at birth, which progresses to single or multiple cell acinar cell carcinomas
• increased pancreas weight is general indicator of tumor burden, but in many animals 15 weeks of age or older, pancreas weights do not increase presumably due to cachexia
• mice develop pancreatic tumors that can be grossly visualized at 9 weeks of age
• at 18 and 21 weeks, mice develop large solid tumor masses of less differentiated acinar cell carcinomas
• pancreas consists of acinar cell microadenomas
• pancreas consists of acinar cell carcinomas; well-differentiated acinar cell carcinomas are observed

immune system
N
• nonimmunized mice develop anti-MUC1 cytotoxic T lymphocytes by 12 weeks and show 80% lysis of MUC1-expressing target cells by 18 weeks




Genotype
MGI:3777580
tg2
Allelic
Composition
Tg(Ela1-TAg*)79Mjt/0
Genetic
Background
involves: C57BL/6 * DBA/2
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
mortality/aging
• almost all mice develop life-threatening tumors and become moribund between 16 and 31 weeks of age

growth/size/body
• many animals show evidence of abdominal distention from tumor formation

neoplasm
• mice develop single or multiple pancreatic tumors; one large or multiple small tumors are found within or replacing the pancreas
• tumors are soft and gray with multiple red cystic or hemorrhagic foci
• animals examined between 16 and 26 weeks display acinar cell adenomas and dysplastic acinar cells
• pancreas consists of acinar cell carcinoma cells instead of normal tissue in some severe cases
• mice examined at 10 and 16 weeks of age show pancreatic acinar cell carcinomas
• in some mice, largest tumors metastasize to liver, and in some cases to the mesenteric lymph nodes or serosa of diaphragm

endocrine/exocrine glands
• in larger tumors, foci of necrosis almost completely replaced normal pancreas tissue
• pancreatic tissue between tumors is dense, firm and whiter than normal, containing multiple foci of small hemorrhagic cysts
• normal acinar tissue is absent when pancreas of each tumor-bearing animal is examined
• newborn transgenic mice display lack of normal pancreas tissue and show only dysplastic acinar tissue
• mice develop single or multiple pancreatic tumors; one large or multiple small tumors are found within or replacing the pancreas
• tumors are soft and gray with multiple red cystic or hemorrhagic foci
• animals examined between 16 and 26 weeks display acinar cell adenomas and dysplastic acinar cells
• pancreas consists of acinar cell carcinoma cells instead of normal tissue in some severe cases
• mice examined at 10 and 16 weeks of age show pancreatic acinar cell carcinomas





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last database update
12/10/2024
MGI 6.24
The Jackson Laboratory