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Phenotypes Associated with This Genotype
Genotype
MGI:3720100
Allelic
Composition
Lats2tm1Noj/Lats2tm1Noj
Genetic
Background
involves: 129S2/SvPas * C57BL/6
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Lats2tm1Noj mutation (1 available); any Lats2 mutation (44 available)
phenotype observed in females
phenotype observed in males
N normal phenotype

Lats2tm1Noj/Lats2tm1Noj embryos exhibit severe nervous system developmental defects

mortality/aging
• while 30 embryos are recovered at E10.5, only 3 embryos are recovered at E11.5 and none are recovered at E12.5 or later

embryo
• at E13.5, branchial arches exhibit delayed development
• at E13.5, growth retardation is evident in the whole embryo and in a number of organs including branchial arches and skeletal muscle

cellular
• 24% of mouse embryonic fibroblasts contain an increase in centrosome number (greater than 2 per cell) where 7.6% of wild-type cells have greater than 2 centrosomes
• 15.1% of mouse embryonic fibroblasts have an enlarged nucleus compared to only 1.7% of wild-type cells
• 3.4-fold more mouse fibroblast cells are multinucleated relative to wild-type cells
• some mouse embryonic fibroblast cells show polyploidy
• the number mouse embryonic fibroblast cells that fail cytokinesis is increased 3.3-fold relative to wild-type cells
• mouse embryonic fibroblast cells exit mitosis faster than wild-type cells
• at E13.5, apoptotic cells are observed in the spinal cord

nervous system
• at E13.5, apoptotic cells are observed in the spinal cord
• at E13.5, surviving mice have a reduced number of nerve cells in the neuroepithelial layer of the fourth ventricle as well as infiltration of inflammatory cells
• at E13.5, the neuroepithelial layer is thinner and contains many pyknotic cells
• at E10.5 and E13.5, spinal cords have reduced number of nerve cells and the density of nerve fibers

muscle
• at E13.5, skeletal muscle development is delayed

growth/size/body
• at E13.5, growth retardation is evident in the whole embryo and in a number of organs including branchial arches and skeletal muscle

cardiovascular system
• at E13.5, surviving mice have small hearts with only modest developmental retardation

craniofacial
• at E13.5, branchial arches exhibit delayed development


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
12/17/2024
MGI 6.24
The Jackson Laboratory