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Phenotypes Associated with This Genotype
Genotype
MGI:3623770
Allelic
Composition
Tbx5tm1Jse/Tbx5tm1Jse
Tg(Prrx1-cre)1Cjt/0
Genetic
Background
involves: C57BL/6J * SJL/J
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Tbx5tm1Jse mutation (0 available); any Tbx5 mutation (28 available)
Tg(Prrx1-cre)1Cjt mutation (2 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
growth/size/body
• due to absence of the sternum, the ribcage fails to close and associated herniation of internal organs and failure of abdominal body wall closure is seen

mortality/aging

limbs/digits/tail
• no limb outgrowth and morphologically distinguishable apical ectodermal ridge are visible in the forelimb region; limb defect is manifest by E10.5
• cells of the prospective forelimb undergo extensive apoptosis by E9.5
• at E10.5
• forelimbs of newborns are completely absent, however the hindlimbs are unaffected (J:83258)
• some newborns have a small, rudimentary flap of skin on one side of the embryo where the forelimb would normally form (J:83258)

skeleton
• ribcage fails to fuse (J:83258)
• due to absence of the sternum, the ribcage fails to close (J:217810)
• mice completely lack a sternum (J:217810)
• sternal bands do not form in E12.5-E13.5 embryos (J:217810)

embryo
• cells of the prospective forelimb undergo extensive apoptosis by E9.5
• no limb outgrowth and morphologically distinguishable apical ectodermal ridge are visible in the forelimb region; limb defect is manifest by E10.5
• at E10.5


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