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Phenotypes associated with this allele
Allele Symbol
Allele Name
Allele ID
Bnc2Gt(pU21)18Imeg
gene trap 18, Institute of Molecular Embryology and Genetics
MGI:3639337
Summary 1 genotype
Jump to Allelic Composition Genetic Background Genotype ID
hm1
Bnc2Gt(pU21)18Imeg/Bnc2Gt(pU21)18Imeg involves: C57BL/6 * CBA MGI:4421509


Genotype
MGI:4421509
hm1
Allelic
Composition
Bnc2Gt(pU21)18Imeg/Bnc2Gt(pU21)18Imeg
Genetic
Background
involves: C57BL/6 * CBA
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Bnc2Gt(pU21)18Imeg mutation (2 available); any Bnc2 mutation (129 available)
phenotype observed in females
phenotype observed in males
N normal phenotype

Small head, cleft palate and tongue abnormalities in Bnc2Gt(pU21)18Imeg/Bnc2Gt(pU21)18Imeg mice

mortality/aging
• mice die within 24 hours of birth

craniofacial
• an abnormally large posterior fontanel is clearly visible in newborns
• an excessively wide sagittal suture is clearly visible in newborns
• diminished growth of the frontal bones
• diminished growth of the parietal bones
• the size of the alisphenoid is reduced
• the internal pterygoid processes have not extended caudally
• fails to grow towards the midline and extend cranially unlike in wild-type mice
• the palatine bone is virtually absent in newborns
• at E14.5 and E16.5, the number of mesenchyme cells in metaphase, anaphase, or telophase in the palatal processes is decreased 50% compared to in wild-type mice
• however, the number of cells undergoing apoptosis is normal
• 50% of mice exhibit a complete cleft secondary palate and the other 50% exhibit a posterior-only cleft secondary palate unlike in wild-type mice
• at E16.5 and P0

growth/size/body
• fails to grow towards the midline and extend cranially unlike in wild-type mice
• at E14.5 and E16.5, the number of mesenchyme cells in metaphase, anaphase, or telophase in the palatal processes is decreased 50% compared to in wild-type mice
• however, the number of cells undergoing apoptosis is normal
• 50% of mice exhibit a complete cleft secondary palate and the other 50% exhibit a posterior-only cleft secondary palate unlike in wild-type mice
• at E16.5 and P0
• aerial distention of the digestive tract is observed at birth
• at E16.5, E18.5, and P0

skeleton
• an abnormally large posterior fontanel is clearly visible in newborns
• an excessively wide sagittal suture is clearly visible in newborns
• diminished growth of the frontal bones
• diminished growth of the parietal bones
• the size of the alisphenoid is reduced
• the internal pterygoid processes have not extended caudally
• fails to grow towards the midline and extend cranially unlike in wild-type mice
• the palatine bone is virtually absent in newborns

digestive/alimentary system
• fails to grow towards the midline and extend cranially unlike in wild-type mice
• at E14.5 and E16.5, the number of mesenchyme cells in metaphase, anaphase, or telophase in the palatal processes is decreased 50% compared to in wild-type mice
• however, the number of cells undergoing apoptosis is normal
• 50% of mice exhibit a complete cleft secondary palate and the other 50% exhibit a posterior-only cleft secondary palate unlike in wild-type mice
• at E16.5 and P0
• aerial distention of the digestive tract is observed at birth





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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
11/19/2024
MGI 6.24
The Jackson Laboratory