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Phenotypes Associated with This Genotype
Genotype
MGI:3582674
Allelic
Composition
ApcMin/Apc+
Blmtm1Grdn/Blm+
Genetic
Background
involves: 129P2/OlaHsd * 129S/SvEv * Black Swiss * C57BL/6J
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
ApcMin mutation (12 available); any Apc mutation (158 available)
Blmtm1Grdn mutation (0 available); any Blm mutation (88 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
neoplasm
• developed twice as many gastrointestinal adenomas as single heterozygous Apc mutant mice (31.4 tumors/mouse vs. 14.2 tumors/mouse in wildtype), however tumors were similar in size
• developed low- and high-grade adenomas in the small intestine, whereas only low-grade adenomas were seen in heterozygous Apc mutant mice
• all colonic adenomas displayed high-grade dysplasia

digestive/alimentary system
• developed twice as many gastrointestinal adenomas as single heterozygous Apc mutant mice (31.4 tumors/mouse vs. 14.2 tumors/mouse in wildtype), however tumors were similar in size
• developed low- and high-grade adenomas in the small intestine, whereas only low-grade adenomas were seen in heterozygous Apc mutant mice
• all colonic adenomas displayed high-grade dysplasia

Mouse Models of Human Disease
DO ID OMIM ID(s) Ref(s)
Bloom syndrome DOID:2717 OMIM:210900
J:79058


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
11/19/2024
MGI 6.24
The Jackson Laboratory