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Phenotypes associated with this allele
Allele Symbol
Allele Name
Allele ID
Apctm3Mmt
targeted mutation 3, Makoto M Taketo
MGI:2449944
Summary 4 genotypes
Jump to Allelic Composition Genetic Background Genotype ID
hm1
Apctm3Mmt/Apctm3Mmt involves: 129X1/SvJ * C57BL/6N MGI:3606987
ht2
Apctm3Mmt/Apc+ B6.129X1-Apctm3Mmt MGI:3606986
ht3
Apctm3Mmt/Apc+ involves: 129X1/SvJ * C57BL/6N MGI:3811542
ht4
Apctm2Mmt/Apctm3Mmt involves: 129X1/SvJ * C57BL/6N MGI:3811543


Genotype
MGI:3606987
hm1
Allelic
Composition
Apctm3Mmt/Apctm3Mmt
Genetic
Background
involves: 129X1/SvJ * C57BL/6N
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Apctm3Mmt mutation (0 available); any Apc mutation (158 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
mortality/aging
• embryos first appear abnormal at E7.5 and fail to turn by E9.5
• no homozygous mice born

embryo
• at E8.5, an abnormal anterior region is displaced outside the yolk sac
• at E9.5, both the anterior and ventral regions appear abnormal
• unturned at E9.5
• impaired formation of axial mesendoderm
• anterior truncation at E8.5
• partial axis duplication
• head folds are missing
• at E9.5, the neural tube appears deformed
• floor plate is duplicated at the anterior end
• notochord is duplicated at the anterior end
• at E7.5, the node is disorganized and expanded, leading to secondary axis formation
• constricted appearance at the border between embryonic and extraembryonic tissue at E7.5
• impaired formation of anterior visceral endoderm

nervous system
• at E9.5, the neural tube appears deformed
• floor plate is duplicated at the anterior end
• at E8.5, the brain is poorly formed, although some neural ectoderm is observed
• brain is truncated in the anterior hindbrain or caudal midbrain
• part but not all of the hindbrain missing
• missing midbrain
• missing forebrain

cardiovascular system
• at E9.5, heart tubes remain on the dorsal side of the unturned embryo and fuse only partially
• failure of the cardiac mesoderm to fuse at the ventral midline

digestive/alimentary system
• foregut fails to form properly

growth/size/body
• at E8.5, an abnormal anterior region (head) is displaced outside the yolk sac




Genotype
MGI:3606986
ht2
Allelic
Composition
Apctm3Mmt/Apc+
Genetic
Background
B6.129X1-Apctm3Mmt
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Apctm3Mmt mutation (0 available); any Apc mutation (158 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
digestive/alimentary system
• intesinal polyps are dysplastic adenomas
• an average of 0.26 polyps per mouse at 15 months of age

neoplasm
• intesinal polyps are dysplastic adenomas




Genotype
MGI:3811542
ht3
Allelic
Composition
Apctm3Mmt/Apc+
Genetic
Background
involves: 129X1/SvJ * C57BL/6N
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Apctm3Mmt mutation (0 available); any Apc mutation (158 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
digestive/alimentary system
• unlike Apctm1Mmt homozygotes, mice display few intestinal polyps




Genotype
MGI:3811543
ht4
Allelic
Composition
Apctm2Mmt/Apctm3Mmt
Genetic
Background
involves: 129X1/SvJ * C57BL/6N
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Apctm2Mmt mutation (0 available); any Apc mutation (158 available)
Apctm3Mmt mutation (0 available); any Apc mutation (158 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
embryo
• at E7.5, the anterior embryonic region is protruding from the yolk sac; more prominent at E8.5
• at E6.5, embryonic ectoderm cells remain only in the distal region
• however, visceral endoderm develops normally





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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
12/10/2024
MGI 6.24
The Jackson Laboratory