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Phenotypes Associated with This Genotype
Genotype
MGI:2654883
Allelic
Composition
\Tulp3tm1Jng/\Tulp3+
Genetic
Background
involves: 129S1/Sv * 129X1/SvJ * C57BL/6J
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Tulp3tm1Jng mutation (2 available); any Tulp3 mutation (52 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
mortality/aging
• affected heterozygous mutant embryos exhibit embryonic lethality with excessive neuroepithelial apoptosis in the hindbrain
• however, no overt abnormalities are detected in live-born heterozygous mutant mice

nervous system
• at E10.5, affected heterozygous mutant embryos display excessive apoptosis of neuroepithelial cells in the hindbrain region
• at E10.5, a few heterozygotes exhibit an open neural tube
• at E10.5, 18% of heterozygous mutant embryos display an abnormal brain phenotype that is less severe than that observed in homozygous mutant embryos
• at E10.5, the majority of affected heterozygous mutant embryos display abnormal fore-, mid- and hindbrain development
• at E10.5, affected heterozygotes exhibit an underdeveloped and disorganized midbrain
• at E10.5, affected heterozygotes exhibit an underdeveloped and disorganized forebrain
• at E10.5, affected heterozygotes exhibit an underdeveloped and disorganized hindbrain with a collapsed roof

cardiovascular system
• some heterozygous mutant embryos display sites of hemorrhage at E12.5 and blood loss at E14.5

embryo
• at E10.5, a few heterozygotes exhibit an open neural tube

cellular
• at E10.5, affected heterozygous mutant embryos display excessive apoptosis of neuroepithelial cells in the hindbrain region


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