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Phenotype Image Detail
Image
Caption A mutation in Plexin-B2 leads to exencephaly. Plxnb2m597804Hubr/Plxnb2m597804Hubr (Plexin-B2E369G) embryos displaying closure defects throughout the brain region of the neural tube (A-C).
Copyright This image is from Wansleeben C, PLoS One 2011;6(4):e19357, and is displayed under the terms of the Creative Commons Attribution 4.0 International License. J:173681
Associated
Alleles
Symbol Name
Plxnb2m597804Hubr plexin B2; mutation 597804, Hubrecht Institute
Associated
Genotypes
Allelic Composition Genetic Background
Plxnb2m597804Hubr/Plxnb2m597804Hubr involves: C57BL/6 * FVB/N

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