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Phenotypes Associated with This Genotype
Genotype
MGI:3575580
Allelic
Composition
ApcMin/Apc+
Recql4tm1Glu/Recql4tm1Glu
Genetic
Background
involves: 129S7/SvEvBrd * C57BL/6J
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
ApcMin mutation (12 available); any Apc mutation (154 available)
Recql4tm1Glu mutation (0 available); any Recql4 mutation (46 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
neoplasm
• the average maximal diameter of macroadenomas was larger than in double heterozygous controls
• at 120 days of age, exhibited a 2-fold increase in the multiplicity of macroadenomas along the entire GI tract compared to double heterozygous mutant controls, however no difference in the mean or maximal lifespan compared to controls
• mutants always developed tumors in the large intestine, a site that is inconsistently affected in double heterozygous controls

digestive/alimentary system
• mutants always developed tumors in the large intestine, a site that is inconsistently affected in double heterozygous controls

Mouse Models of Human Disease
DO ID OMIM ID(s) Ref(s)
Rothmund-Thomson syndrome DOID:2732 OMIM:268400
J:97101


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
04/23/2024
MGI 6.23
The Jackson Laboratory