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Phenotypes Associated with This Genotype
Genotype
MGI:6713511
Allelic
Composition
Apctm1Cip/Apc+
Cdhr5tm1Lex/Cdhr5tm1Lex
Genetic
Background
involves: 129P2/OlaHsd * 129S5/SvEvBrd * C57BL/6
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Apctm1Cip mutation (0 available); any Apc mutation (156 available)
Cdhr5tm1Lex mutation (1 available); any Cdhr5 mutation (28 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
digestive/alimentary system
• at 6-8 months of age, 83% of mice show symptoms of neoplasia (rectal bleeding, anemia, splenomegaly) and 1 or more macroadenomas in the intestinal tract relative to 56% in Apctm1Cip heterozygotes
• a greater % of mice develop 51 to 100 or over 100 polyps (all sizes) in the intestinal tract, and the average number of tumors per mouse is ~3-fold higher than that in Apctm1Cip heterozygotes

neoplasm
• at 6-8 months of age, 83% of mice show symptoms of neoplasia (rectal bleeding, anemia, splenomegaly) and 1 or more macroadenomas in the intestinal tract relative to 56% in Apctm1Cip heterozygotes
• a greater % of mice develop 51 to 100 or over 100 polyps (all sizes) in the intestinal tract, and the average number of tumors per mouse is ~3-fold higher than that in Apctm1Cip heterozygotes
• mice develop more tumors, esp. larger ones, in the intestinal tract; the average number of macroadenomas (>5 mm) per mouse is ~3-fold higher than that in Apctm1Cip heterozygotes
• however, no differences in tumor grade, aggressiveness or proliferation are observed


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
03/25/2025
MGI 6.24
The Jackson Laboratory