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Phenotypes Associated with This Genotype
Genotype
MGI:3696453
Allelic
Composition
Satb2tm1Rug/Satb2tm1Rug
Genetic
Background
Not Specified
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Satb2tm1Rug mutation (0 available); any Satb2 mutation (44 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
cellular
• exhibit defects in osteoblast differentiation
• osteoblasts grown in culture show reduced formation of bone modules, indicating reduced differentiation

mortality/aging
• die immediately after birth

skeleton
• alternations in the temporal processes of the squamous bone
• malformation of the lesser horns and the body of the hyoid bone
• the lesser horns are fused and show no articulation
• incisor teeth are missing at E17.5, although tooth germs are detected at E13.5
• at E18.5, the anterior part of the mandible is missing, however the posterior half appears normal
• shorter lower jaw at E14.5 and E17.5
• severe
• thyroid cartilage is missing from the laryngeal cartilages
• however, the aryenoid, cricoid cartilages and the tracheal rings are normal
• decrease in bone volume/total bone volume
• exhibit defects in osteoblast differentiation
• osteoblasts grown in culture show reduced formation of bone modules, indicating reduced differentiation
• virtual absence of osteoid seams in the trabeculae of developing bones, suggesting defect in extracellular matrix deposition
• trabeculae of bones are shorter and thinner than in wild-type
• decrease in trabeculae number per mm
• however, the growth plate is normal
• E15.5 mutants show delayed bone formation
• E15.5 mutants show delayed bone mineralization
• less mineralization of the maxilla and skull bones

craniofacial
• alternations in the temporal processes of the squamous bone
• malformation of the lesser horns and the body of the hyoid bone
• the lesser horns are fused and show no articulation
• incisor teeth are missing at E17.5, although tooth germs are detected at E13.5
• at E18.5, the anterior part of the mandible is missing, however the posterior half appears normal
• shorter lower jaw at E14.5 and E17.5
• severe
• increased apoptosis in the first branchial arch at E10.5
• the maxillary processes do not converge at the tip of the snout
• palatal shelf mesenchyme generates bulges not seen in wild-type
• at E17.5, the palatal shelves of mutant embryos fail to grow toward the fusion line
• E17.5 mutants have a smaller and shorter tongue
• E17.5 mutants have a shorter tongue

embryo
• increased apoptosis in the first branchial arch at E10.5

limbs/digits/tail
• shorter hindlimbs at E17.5

digestive/alimentary system
• palatal shelf mesenchyme generates bulges not seen in wild-type
• at E17.5, the palatal shelves of mutant embryos fail to grow toward the fusion line
• E17.5 mutants have a smaller and shorter tongue
• E17.5 mutants have a shorter tongue

respiratory system
• thyroid cartilage is missing from the laryngeal cartilages
• however, the aryenoid, cricoid cartilages and the tracheal rings are normal

growth/size/body
• malformation of the lesser horns and the body of the hyoid bone
• the lesser horns are fused and show no articulation
• incisor teeth are missing at E17.5, although tooth germs are detected at E13.5
• at E18.5, the anterior part of the mandible is missing, however the posterior half appears normal
• shorter lower jaw at E14.5 and E17.5
• severe
• the maxillary processes do not converge at the tip of the snout
• palatal shelf mesenchyme generates bulges not seen in wild-type
• at E17.5, the palatal shelves of mutant embryos fail to grow toward the fusion line
• E17.5 mutants have a smaller and shorter tongue
• E17.5 mutants have a shorter tongue


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
07/29/2025
MGI 6.24
The Jackson Laboratory