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Phenotypes Associated with This Genotype
Genotype
MGI:2656633
Allelic
Composition
Amottm1Bhr/Y
Genetic
Background
involves: 129S7/SvEvBrd * C57BL/6
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Amottm1Bhr mutation (0 available); any Amot mutation (11 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
mortality/aging

growth/size/body
• embryos are developmentally delayed by about 6 hours at E7.5 and sometimes up to 12 hours or more at E8

embryo
• visceral endoderm cell migration at the anterior embryonic/extra-embryonic junction is abnormal; although distal-to-proximal migration is observed, the lateral migration of cells is greatly reduced
• ~ 90% of embryos at E7.5 have excessive folds at the cranial limiting furrow region
• the cranial limiting furrow region contains more than two cell layers and is disorganized
• embryos are developmentally delayed by about 6 hours at E7.5 and sometimes up to 12 hours or more at E8
• visceral endoderm accumulates at the cranial limiting furrow of E7.5 mutants

cardiovascular system
• 62% of embryos are hemorrhagic at E7.5

cellular
• visceral endoderm cell migration at the anterior embryonic/extra-embryonic junction is abnormal; although distal-to-proximal migration is observed, the lateral migration of cells is greatly reduced


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
04/09/2024
MGI 6.23
The Jackson Laboratory