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Phenotypes associated with this allele
Allele Symbol
Allele Name
Allele ID
Rac1tm1Jms
targeted mutation 1, Institute of Medical Science, Japan
MGI:1857700
Summary 2 genotypes
Jump to Allelic Composition Genetic Background Genotype ID
hm1
Rac1tm1Jms/Rac1tm1Jms involves: 129S/SvEv * C57BL/6J MGI:3589368
cn2
Emx1tm1(cre)Ito/Emx1+
Rac1tm1Atai/Rac1tm1Jms
involves: 129P2/OlaHsd * 129S/SvEv * C57BL/6 * ICR MGI:3814361


Genotype
MGI:3589368
hm1
Allelic
Composition
Rac1tm1Jms/Rac1tm1Jms
Genetic
Background
involves: 129S/SvEv * C57BL/6J
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Rac1tm1Jms mutation (0 available); any Rac1 mutation (24 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
mortality/aging
• no homozygous mutant fetuses are identified after E9.5

embryo
• at E8.5, homozygotes fail to elongate along the anterior-posterior axis and remain small and spherical
• at E6.5, the embryonic portion of mutant embryos is severely reduced relative to the extraembryonic portion
• at E7.5, the embryonic ectoderm is irregularly folded
• at E7.5, the embryonic ectoderm is abnormally thick
• homozygotes exhibit developmental arrest and apoptosis of newly formed mesodermal cells during gastrulation
• at E8.5, homozygotes display absence of axial structures such as the neural tube and somites
• at E7.5, numerous pyknotic cells and cell fragments are detected in the space between the embryonic ectoderm and visceral endoderm

growth/size/body
• at E6.5, the embryonic portion of mutant embryos is severely reduced relative to the extraembryonic portion

cellular
• at E6.5, a few homozygotes begin to display pyknotic cells and cell fragments in specific areas of the proamniotic cavity and between the epiblast and visceral endoderm




Genotype
MGI:3814361
cn2
Allelic
Composition
Emx1tm1(cre)Ito/Emx1+
Rac1tm1Atai/Rac1tm1Jms
Genetic
Background
involves: 129P2/OlaHsd * 129S/SvEv * C57BL/6 * ICR
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Emx1tm1(cre)Ito mutation (1 available); any Emx1 mutation (34 available)
Rac1tm1Atai mutation (0 available); any Rac1 mutation (24 available)
Rac1tm1Jms mutation (0 available); any Rac1 mutation (24 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
mortality/aging
• fewer than expected mice are present at P18 but the remainder of mice survive into adulthood
• fewer than expected mice are present at P18

nervous system
• mice exhibit reduced formation of interhemispheric commissural connections by inhibition of midline crossing
• however, the posterior and habenular commissures are normal
• myelinated fibers are reduced in the corpus callosum and anterior commissure compared to in control (Rac1tm1Atai/Rac1+ Emx1tm1(cre)Ito/Emx1+) mice
• retrograde dye labeling experiments demonstrate that contralateral projections of the callosal commissural axons are absent
• myelinated fibers are reduced in the corpus callosum and anterior commissure compared to in control (Rac1tm1Atai/Rac1+ Emx1tm1(cre)Ito/Emx1+) mice
• neuron layers of the telencephalon cortex are thinner than in heterozygous controls (Rac1tm1Atai/Rac1+ Emx1tm1(cre)Ito/Emx1+) with sporadic distortions caused by abnormal cell clusters and nerve fibers
• the dentate gyrus is disorganized
• the pyramidal cell layer of the hippocampus is thinner than in control (Rac1tm1Atai/Rac1+ Emx1tm1(cre)Ito/Emx1+) mice
• somatosensory cortex barrels are small in size and irregular in shape compared to in control (Rac1tm1Atai/Rac1+ Emx1tm1(cre)Ito/Emx1+) mice





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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
10/22/2024
MGI 6.24
The Jackson Laboratory