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Phenotype Image Detail
Image
Caption Disruption of Mir10a leads to enhanced intestinal tumorigenesis in ApcMin/Apc+ mice. (D) Left panel shows normal appearing small intestine with characteristic villi and well-ordered distribution of goblet cells together with basal location of epithelial nuclei. Middle panel is a typical example of a low-grade dysplasia in ApcMin/Apc+ (WT) mice with accumulation of irregular goblet cells pattern (arrowheads) and some loss of nuclear polarity (indicated by "+"). Right panel shows a typical ApcMin/Apc+ Mir10atm1.1Ahl/Mir10atm1.1Ahl (KO) high-grade dysplasia with a large area of loss of goblet cells, widespread loss of nuclear polarity, nuclear pleomorphism, and almost complete loss of villus organization (indicated by "*"). Note the transition from lower-grade dysplasia area with highly irregular goblet cell distribution (arrowheads). Scale bar = 100 uM. Whole intestines were paraffin-embedded as "Swiss rolls", sectioned and stained with hematoxylin and eosin. All animals were in a C57BL/6 background and between 110 and 160 days of age.
Copyright This image is from Stadthagen G, PLoS Genet 2013 Oct;9(10):e1003913, and is displayed under the terms of the Creative Commons Attribution 4.0 International License. J:205135
Associated
Alleles
Symbol Name
ApcMin APC, WNT signaling pathway regulator; multiple intestinal neoplasia
Mir10atm1.1Ahl microRNA 10a; targeted mutation 1.1, Anders Lund
Associated
Genotypes
Allelic Composition Genetic Background
ApcMin/Apc+
Mir10atm1.1Ahl/Mir10atm1.1Ahl
B6.Cg-Mir10atm1.1Ahl Apcmin

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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
04/09/2024
MGI 6.23
The Jackson Laboratory