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Phenotype Image Detail
Image
Caption Abnormal axial skeleton formation in E12.5 Apctm1Rsmi/Apctm1Rsmi Tg(Col2a1-cre)1Rsjo/0 (Col2a1-Cre;Apc15lox/15lox) embryos is already detectable at E12.5. (A) Immunostaining for beta-catenin combined with Alcian blue (AB) staining and (B-E) gene expression analysis by in situ hybridization with indicated probes on consecutive transversal sections of the sclerotome of a mutant embryo and control littermate at E12.5. (F-J) Similiar analysis of vertebrae primordia at E14.6. Beta-catenin-positive spindle-shaped cells lacked expression of all indicated chondrogenic and osteogenic markers (arrowheads). Scale bars: 100 um.
Copyright This image is from Miclea RL, BMC Dev Biol 2009;9():26, an open-access article, licensee BioMed Central Ltd. J:149225
Associated
Alleles
Symbol Name
Apctm1Rsmi APC, WNT signaling pathway regulator; targeted mutation 1, Ron Smits
Tg(Col2a1-cre)1Rsjo transgene insertion 1, Randall S Johnson
Associated
Genotypes
Allelic Composition Genetic Background
Apctm1Rsmi/Apctm1Rsmi
Tg(Col2a1-cre)1Rsjo/0
involves: 129P2/OlaHsd * FVB/N

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