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Phenotypes Associated with This Genotype
Genotype
MGI:3624726
Allelic
Composition
Zeb2tm1.2Yhi/Zeb2tm1.2Yhi
Genetic
Background
involves: 129S1/Sv * 129X1/SvJ * CD-1
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Zeb2tm1.2Yhi mutation (1 available); any Zeb2 mutation (78 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
mortality/aging

nervous system
• a sharp boundary between the neural plate and the rest of the ectoderm is absent
• lack postotic vagal level neural crest cells
• neural tube fails to close

embryo
• cranial neural crest cells do not delaminate nor do they initiate migration
• cranial neural crest cells do not delaminate at the junctional zone between the neural and surface ectoderm
• the first branchial arch is missing
• do not undergo embryonic turning
• embryos are severely retarded in growth by E9.5
• a sharp boundary between the neural plate and the rest of the ectoderm is absent
• lack postotic vagal level neural crest cells
• neural tube fails to close

craniofacial
• the first branchial arch is missing

cellular
• cranial neural crest cells do not delaminate nor do they initiate migration
• cranial neural crest cells do not delaminate at the junctional zone between the neural and surface ectoderm

Mouse Models of Human Disease
DO ID OMIM ID(s) Ref(s)
Mowat-Wilson syndrome DOID:0060485 OMIM:235730
J:82084


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
12/10/2024
MGI 6.24
The Jackson Laboratory