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Phenotypes Associated with This Genotype
Genotype
MGI:3622270
Allelic
Composition
Juntm1Wag/Juntm1Wag
Genetic
Background
either: (involves: 129S2/SvPas) or (involves: 129S2/SvPas * C57BL/6)
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Juntm1Wag mutation (0 available); any Jun mutation (12 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
mortality/aging
• homozygotes die between E11.5 and E15.5; no live homozygotes are recovered after E16.5
• homozygotes die between E11.5 and E15.5, with frequent deaths noted at E13.5

liver/biliary system
• at E12.5, homozygotes often display hepatocyte apoptosis
• at E12.5, homozygotes often display hepatocyte necrosis
• at E12.5, homozygotes display absence of developing ducts
• homozygotes exhibit defective fetal hepatogenesis
• at E12.5, mutant livers display a hypoplastic epithelium with rounded, dissociated residual hepatocytes

homeostasis/metabolism
• 5 of 8 E12.5 homozygotes and 2 of 2 E13.5-E14.5 homozygotes exhibit generalized edema

hematopoietic system
• homozygotes show enhanced fetal liver erythropoiesis with elevated numbers of nucleated erythroid cells, resulting in an erythroblastosis-like phenotype

nervous system
• at E12.5, homozygotes exhibit severe edema in the forebrain, as shown by large intercellular spaces

cardiovascular system
• at E12.5, 1 of 8 homozygotes exhibited severely congested vessels and signs of early liver damage

endocrine/exocrine glands
• at E12.5, homozygotes display absence of developing ducts

cellular
• at E12.5, homozygotes often display hepatocyte apoptosis
• at E12.5, homozygotes often display hepatocyte necrosis


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
04/30/2024
MGI 6.23
The Jackson Laboratory