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Phenotypes Associated with This Genotype
Genotype
MGI:3656076
Allelic
Composition
Dag1tm1Kcam/Dag1tm1Kcam
Genetic
Background
involves: 129S1/Sv * 129X1/SvJ * C57BL/6J
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Dag1tm1Kcam mutation (1 available); any Dag1 mutation (109 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
mortality/aging
• most homozygotes are substantially resorbed by E10.5

embryo
• homozygotes fail to gastrulate
• homozygotes fail to progress beyond the early egg cylinder stage of development
• however, early differentiation of extraembryonic lineages and implantation appear unaffected
• by E7.5, homozygous mutant embryos are much smaller than wild-type embryos
• starting at E6.5, homozygotes typically have a significantly smaller embryonic region
• only a small mass of embryonic tissue is detected at E10.5
• at E7.5, homozygotes lack any identifiable mesodermal tissue
• at E6.5, homozygotes lack any significant development of extraembryonic ectoderm
• in contrast, visceral endoderm and a well-formed pro-amniotic cavity are clearly evident
• at E6.5, homozygotes lack a continuous Reichert's membrane; maternal red blood cells are thus found in the yolk sac cavity as early as E5.5
• only occasional "patches" of laminin and collagen IV, two major structural elements of Reichert's membrane, are detected
• in contrast, the basement membrane between the visceral endoderm and ectoderm appears normal
• Reichert's membrane defects are not due to a lack of parietal endoderm

growth/size/body
• by E7.5, homozygous mutant embryos are much smaller than wild-type embryos


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
06/12/2024
MGI 6.13
The Jackson Laboratory