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Phenotypes Associated with This Genotype
Genotype
MGI:5636659
Allelic
Composition
ApcMin/Apc+
Msh2tm1Mak/Msh2tm1Mak
Genetic
Background
involves: 129P2/OlaHsd * C57BL/6J
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
ApcMin mutation (12 available); any Apc mutation (154 available)
Msh2tm1Mak mutation (1 available); any Msh2 mutation (95 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
mortality/aging
• mice become moribound and die from anemia and intestinal obstruction at a mean age of 82 days

neoplasm
• mice exhibit accelerated intestinal tumorigenesis compared to single ApcMin heterozygous mice, with a large increase in number of small and large bowel adenomas that develop
• an average of 333 adenomas are seen in 10 mutants at 47-78 days of age compared to a mean of 48 adenomas in single ApcMin heterozygotes

digestive/alimentary system
• mice exhibit accelerated intestinal tumorigenesis compared to single ApcMin heterozygous mice, with a large increase in number of small and large bowel adenomas that develop
• an average of 333 adenomas are seen in 10 mutants at 47-78 days of age compared to a mean of 48 adenomas in single ApcMin heterozygotes
• due to tumors

hematopoietic system
• mutants exhibit enhanced polyp formation in the small intestine and colon at 6 weeks of age compared to double heterozygous mice
• treatment with the Nos2 (iNOS) inhibitor L-NIL has no effect on polyp number

Mouse Models of Human Disease
DO ID OMIM ID(s) Ref(s)
colorectal cancer DOID:9256 OMIM:114500
J:75393 , J:200824


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
05/07/2024
MGI 6.23
The Jackson Laboratory