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Phenotypes Associated with This Genotype
Genotype
MGI:5583019
Allelic
Composition
Apctm1Rsmi/Apctm1Rsmi
Pgrtm2(cre)Lyd/Pgr+
Genetic
Background
involves: 129P2/OlaHsd * 129S1/Sv * 129X1/SvJ * C57BL/6J
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Apctm1Rsmi mutation (1 available); any Apc mutation (154 available)
Pgrtm2(cre)Lyd mutation (0 available); any Pgr mutation (73 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
neoplasm
• 62.5% of mice develop endometrioid tubal tumors in distal and fimbrial parts of the oviduct showing severe nuclear atypia, subnuclear vacuolization, abnormal proliferation, complete loss of normal oviduct architecture and compression of the lumen
• tumors resemble human endometrioid tubal cancer
• 27.9% of mice develop endometrioid ovarian tumors which may originate form the endometrioid ovarian cysts, resembling human endometrioid ovarian cancer
• 1 of 43 mice develop a granulosa cell tumor which is distinct from the endometrioid tubal cancer

reproductive system
• 62.5% of mice develop endometrioid tubal tumors in distal and fimbrial parts of the oviduct showing severe nuclear atypia, subnuclear vacuolization, abnormal proliferation, complete loss of normal oviduct architecture and compression of the lumen
• tumors resemble human endometrioid tubal cancer
• 27.9% of mice develop endometrioid ovarian tumors which may originate form the endometrioid ovarian cysts, resembling human endometrioid ovarian cancer
• 1 of 43 mice develop a granulosa cell tumor which is distinct from the endometrioid tubal cancer
• 9.4% of mice show extraovarian endometrioid lesions within the utero-ovarian ligament, next to the tubal and ovarian tumors
• 16.3% of mice show ovarian endometrioid cysts, mostly in younger mice
• 87.2% of mice exhibit tubular intraepithelial lesions in the epithelium of the distal oviduct and fimbriae
• lesions show loss of cilia, bulging of cells into the lumen, layering and suspicious stratification of cells, and rounding and hyperchromatization of the nucleus
• 20% of mice develop glandular transformation of the normal papillary architecture of the oviduct characterized by glandular growth, loss of cilia, and general loss of normal cellular morphology
• presence of extraovarian endometrioid lesions coincide with lesions found in the oviduct and ovary

endocrine/exocrine glands
• 16.3% of mice show ovarian endometrioid cysts, mostly in younger mice
• 27.9% of mice develop endometrioid ovarian tumors which may originate form the endometrioid ovarian cysts, resembling human endometrioid ovarian cancer
• 1 of 43 mice develop a granulosa cell tumor which is distinct from the endometrioid tubal cancer

growth/size/body
• 16.3% of mice show ovarian endometrioid cysts, mostly in younger mice

Mouse Models of Human Disease
DO ID OMIM ID(s) Ref(s)
ovarian cancer DOID:2394 OMIM:167000
OMIM:607893
J:210095


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