About   Help   FAQ
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)
Citing These Resources
Funding Information
Warranty Disclaimer, Privacy Notice, Licensing, & Copyright
Send questions and comments to User Support.
last database update
11/12/2024
MGI 6.24
The Jackson Laboratory