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Phenotypes Associated with This Genotype
Genotype
MGI:3794074
Allelic
Composition
Grhl3ct/?
Vangl2Lp/Vangl2+
Genetic
Background
involves: A * GFF
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Grhl3ct mutation (2 available); any Grhl3 mutation (53 available)
Vangl2Lp mutation (2 available); any Vangl2 mutation (30 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
nervous system
• at E16.5 and E18.5 mice with meningomyelocele display increased astrocyte staining compared to in wild-type mice
• mice exhibit meningomyelocele
• in mice with meningomyelocele, the dorsal region of the neural tube lays laterally to the ventral horn and the dorsal white matter is moved into a ventrolateral position unlike in wild-type mice
• at E16.5, the number of neuronal cells in the meningomyelocele placode is decreased compared to in wild-type mice

behavior/neurological
• mice exhibit meningomyelocele with hypotonic hindlimbs with spontaneous and extensive movement of the hip and knee joints but only slight movement at the ankle joints
• mice do not display coordination between fore- and hindlimbs
• mice occasionally exhibit plantar steps that demonstrate the ability to support their body weight

growth/size/body
• mice with meningomyelocele exhibit reduced fetal weight

skeleton
• mice exhibit meningomyelocele

embryo
• mice exhibit meningomyelocele

cellular
• at E16.5 and E18.5 mice with meningomyelocele display increased astrocyte staining compared to in wild-type mice


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
12/30/2025
MGI 6.24
The Jackson Laboratory