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Phenotypes Associated with This Genotype
Genotype
MGI:7344038
Allelic
Composition
Men1tm1.2Ctre/Men1tm1.2Ctre
H2az2Tg(Wnt1-cre)11Rth/H2az2+
Genetic
Background
involves: 129S6/SvEvTac * C57BL/6J * CBA/J
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
H2az2Tg(Wnt1-cre)11Rth mutation (2 available); any H2az2 mutation (25 available)
Men1tm1.2Ctre mutation (1 available); any Men1 mutation (40 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
mortality/aging

behavior/neurological

craniofacial
• skeletal staining revealed the absence of ossified palatal shelves
• newborns exhibit unfused palatal shelves
• all newborns exhibit a bilateral cleft of the secondary palate

skeleton
N
• newborn pups do NOT exhibit rib or sternum defects
• skeletal staining revealed the absence of ossified palatal shelves

digestive/alimentary system
• skeletal staining revealed the absence of ossified palatal shelves
• newborns exhibit unfused palatal shelves
• all newborns exhibit a bilateral cleft of the secondary palate

growth/size/body
• skeletal staining revealed the absence of ossified palatal shelves
• newborns exhibit unfused palatal shelves
• all newborns exhibit a bilateral cleft of the secondary palate


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
01/06/2026
MGI 6.24
The Jackson Laboratory