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Phenotype Image Detail
Image
Caption Abnormalities of Stac3tm1a(KOMP)Wtsi/Stac3tm1a(KOMP)Wtsi (KO) mice. (A) Complete paralysis, wrist drop, and abnormally rounded lunar appearance of a newborn mutant mouse. (B) Alveoli of mutant lungs are not inflated, as shown by Masson's trichrome staining. (C) Whole-mount E18.5 skeletons prepared with alcian blue, a cartilage stain, and alizarin red S, a bone stain, show numerous abnormalities in mutants, including abnormal spinal curvature, growth defects in costal cartilages, and decreased bone formation at muscle insertion sites. (D) H&E sagittal paraffin sections of E16.5 heads show decreased muscle mass of the tongue and abnormal clustering of nuclei in mutants. Mutant fibers also have fewer observable striations, and most have a vacuolated appearance. (E) Electron microscopy of E15.5 tongues shows that sarcomeres are present in mutant fibers as seen here but overall, sarcomeres appear more disorganized. (Scale bars, 1 um.)
Copyright This image is from Nelson BR, Proc Natl Acad Sci U S A 2013 Jul 16;110(29):11881-6. Copyright 2013 National Academy of Sciences, U.S.A. J:222015
Associated
Alleles
Symbol Name
Stac3tm1a(KOMP)Wtsi SH3 and cysteine rich domain 3; targeted mutation 1a, Wellcome Trust Sanger Institute
Stac3tm1a(KOMP)Wtsi SH3 and cysteine rich domain 3; targeted mutation 1a, Wellcome Trust Sanger Institute
Associated
Genotypes
Allelic Composition Genetic Background
Stac3tm1a(KOMP)Wtsi/Stac3tm1a(KOMP)Wtsi involves: C57BL/6N

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
04/30/2024
MGI 6.23
The Jackson Laboratory