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Phenotypes Associated with This Genotype
Genotype
MGI:2175907
Allelic
Composition
Apctm1Mmt/Apc+
Genetic
Background
involves: 129S2/SvPas * C57BL/6J
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Apctm1Mmt mutation (0 available); any Apc mutation (154 available)
phenotype observed in females
phenotype observed in males
N normal phenotype

Nascent intestinal polyps in Apctm1Mmt/Apc+ mice

neoplasm
• intestinal polyps are polyploid, papillary, or sessile adenoma; every polyp consists of a microadenoma covered with a normal layer of villous epithelium (J:25200)
• increase in incidence follows loss of normal Apc allele in nascent polyps (J:25200)
• numerous intestinal tumors develop in homozygotes (J:79668)
• most tumors are small; one animal developed a tumor >6 mm in diameter (J:79668)

digestive/alimentary system
• multiple polyps develop soon after birth; all heterozygotes develop polyps by 7 weeks of age and numbers increase with age
• polyps are found from duodenum to rectum, mainly in small intestine
• intestinal polyps are polyploid, papillary, or sessile adenoma; every polyp consists of a microadenoma covered with a normal layer of villous epithelium (J:25200)
• increase in incidence follows loss of normal Apc allele in nascent polyps (J:25200)
• numerous intestinal tumors develop in homozygotes (J:79668)
• most tumors are small; one animal developed a tumor >6 mm in diameter (J:79668)

Mouse Models of Human Disease
DO ID OMIM ID(s) Ref(s)
familial adenomatous polyposis DOID:0050424 OMIM:PS175100
J:25200


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
04/16/2024
MGI 6.23
The Jackson Laboratory