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Phenotypes Associated with This Genotype
Genotype
MGI:2175762
Allelic
Composition
Cdkn1ctm1Bbd/Cdkn1ctm1Bbd
Genetic
Background
involves: 129S1/Sv * 129X1/SvJ * C57BL/6
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Cdkn1ctm1Bbd mutation (1 available); any Cdkn1c mutation (19 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
mortality/aging
• most homozygotes die within a few hours of birth
• about 10.6% of homozygotes born alive are morphologically and behaviorally normal and survive into adulthood

behavior/neurological
• difficulty suckling as determined by absence of milk in the stomach

skeleton
• higher density of chondrocytes
• delayed terminal differentiation of chondrocytes in endochondral bone

craniofacial
• failure of palatal shelves to grow and meet at the midline, possibly due to apoptotic cells
• at E14.5, mutants show increased apoptosis of epithelial cells on the surface of the palatal shelves and in the mesenchyme located at the base of the palatal shelves
• observed in about half of live births

digestive/alimentary system
• failure of palatal shelves to grow and meet at the midline, possibly due to apoptotic cells
• at E14.5, mutants show increased apoptosis of epithelial cells on the surface of the palatal shelves and in the mesenchyme located at the base of the palatal shelves
• observed in about half of live births
• increased apoptosis in the smooth muscle layer of the intestine
• about half of live births with inflated gastrointestinal tract
• 40% of live births with grossly shortened intestinal tract, independent of presence or absence of cleft palate
• may end blindly and open to the abdominal cavity
• at least partially absent in mice that die in the first day of life
• distal end may be open to the abdominal cavity
• often absent in mice that die in the first day of life
• in half of animals born live, an inflated gastrointestinal tract is seen

nervous system
• apoptotic cell death in the ventral midbrain is increased 2 fold at E18.5
• tyrosine hydroxylase is reduced in the ventral midbrain at E18.5

limbs/digits/tail
• short limbs at birth in those mice that die early

growth/size/body
• failure of palatal shelves to grow and meet at the midline, possibly due to apoptotic cells
• at E14.5, mutants show increased apoptosis of epithelial cells on the surface of the palatal shelves and in the mesenchyme located at the base of the palatal shelves
• observed in about half of live births
• in half of animals born live, an inflated gastrointestinal tract is seen

cellular
• apoptotic cell death in the ventral midbrain is increased 2 fold at E18.5

Mouse Models of Human Disease
DO ID OMIM ID(s) Ref(s)
NOT Beckwith-Wiedemann syndrome DOID:5572 OMIM:130650
J:40142


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
04/23/2024
MGI 6.23
The Jackson Laboratory