About   Help   FAQ
Phenotypes Associated with This Genotype
Genotype
MGI:5467642
Allelic
Composition
H2-Oa/Brd2Tg(otx2-lacZ)F5pImat/H2-Oa/Brd2Tg(otx2-lacZ)F5pImat
Genetic
Background
involves: CD-1
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
H2-Oa/Brd2Tg(otx2-lacZ)F5pImat mutation (0 available); any H2-Oa mutation (11 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
mortality/aging

embryo
• in most mice at E10.5
• cranial neural tube defects in most mice at E10.5
• severely distorted at the level of the rostral rhombencephalon
• neuroepithelial cells exhibit impaired differentiation with failure to exit the cell cycle compared with wild-type cells
• irregularly thickened at the level of the rostral rhombencephalon

nervous system
• increased cell death in the neuroepithelium at E10.5
• cranial neural tube defects in most mice at E10.5
• severely distorted at the level of the rostral rhombencephalon
• neuroepithelial cells exhibit impaired differentiation with failure to exit the cell cycle compared with wild-type cells
• irregularly thickened at the level of the rostral rhombencephalon

craniofacial
• in most mice at E10.5

growth/size/body
• in most mice at E10.5

cellular
• neuroepithelial cells exhibit impaired differentiation with failure to exit the cell cycle compared with wild-type cells
• increased cell death in the neuroepithelium 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)
Citing These Resources
Funding Information
Warranty Disclaimer, Privacy Notice, Licensing, & Copyright
Send questions and comments to User Support.
last database update
03/25/2025
MGI 6.24
The Jackson Laboratory