About   Help   FAQ
Phenotype Image Detail
Image
Caption Skeletogenesis is severely impaired in Apctm1Rsmi/Apctm1Rsmi Tg(Col2a1-cre)1Rsjo/0 (Col2a1-cre;Apc15lox/15lox) mice. (A-E) Greatly impaired skeletal development and growth arrest of mutant embryos. Gross appearance (A-C) and Alcian blue and Alizarin red staining (D-E) of skeletal preparations of mutant embryos and control littermates at indicated developmental stages. Conditional Apc mutants showed lack of mandible outgrowth (arrowheads), poor limb development (black arrows), and an open thoracic and abdominal cavity (red arrows). Scale bars: 1 mm.
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
04/16/2024
MGI 6.23
The Jackson Laboratory