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Phenotypes Associated with This Genotype
Genotype
MGI:3513849
Allelic
Composition
Apctm1Cip/Apc+
Genetic
Background
involves: 129P2/OlaHsd * C57BL/6
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Apctm1Cip mutation (0 available); any Apc mutation (158 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
mortality/aging
• heterozygotes begin to die at 4 months of age with 50% dying by 6 months of age

neoplasm
• in situ carcinomas are seen in both the small and large intestines
• over 50% of lesions in mutants over 12 months of age are tubular adenomas harboring invasive carcinomas
• small and large adenomas are seen throughout the intestine
• the number of polyps is increased and the distribution of polyps shifted towards the ileum under specific pathogen-free conditions
• compared to ApcMin heterozygotes more lesions are see in the colon, however the overall number of lesions is the same in both lines
• 9% of heterozygotes developed mammary adenocanthomas

cardiovascular system
• first seen around 4 months of age, associated with decreased life span

digestive/alimentary system
• first seen around 4 months of age, associated with decreased life span
• rectal prolapse, associated with more severe polyposis in the colon, is seen as early as 4 months of age and is seen in 61% of surviving mutants by 6 months of age
• the prolapse is highly dysplatic and in 10% of these dysplatic areas adenocarcinoma is also seen
• fewer mutants raised in specific pathogen-free conditions developed rectal prolapse
• in situ carcinomas are seen in both the small and large intestines
• over 50% of lesions in mutants over 12 months of age are tubular adenomas harboring invasive carcinomas
• small and large adenomas are seen throughout the intestine
• the number of polyps is increased and the distribution of polyps shifted towards the ileum under specific pathogen-free conditions
• compared to ApcMin heterozygotes more lesions are see in the colon, however the overall number of lesions is the same in both lines

hematopoietic system
• first seen around 4 months of age, associated with decreased life span

endocrine/exocrine glands
• 9% of heterozygotes developed mammary adenocanthomas

integument
• 9% of heterozygotes developed mammary adenocanthomas


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
11/05/2024
MGI 6.24
The Jackson Laboratory