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Phenotypes Associated with This Genotype
Genotype
MGI:2684380
Allelic
Composition
Grhl3ct/Grhl3tm1Jane
Genetic
Background
involves: 129S1/Sv * C57BL/6 * STOCK ct/J
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Grhl3ct mutation (2 available); any Grhl3 mutation (53 available)
Grhl3tm1Jane mutation (1 available); any Grhl3 mutation (53 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
nervous system
• the incidence of spina bifida in these embryos was higher than reported for ct homozygotes (31% vs 12%, respectively)
• the extent of the spina bifida more closely resembled ct (lumbosacral spina bifida) than the null allele (thorocolumbosacral)
• 14% of the mice had tail flexion defects only
• 5% of mice with this genotype were normal

embryo
• the incidence of spina bifida in these embryos was higher than reported for ct homozygotes (31% vs 12%, respectively)
• the extent of the spina bifida more closely resembled ct (lumbosacral spina bifida) than the null allele (thorocolumbosacral)
• 14% of the mice had tail flexion defects only
• 5% of mice with this genotype were normal


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
03/25/2025
MGI 6.24
The Jackson Laboratory