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Phenotypes Associated with This Genotype
Genotype
MGI:3690622
Allelic
Composition
Fgatm1Jld/Fgatm1Jld
Plgtm1Jld/Plgtm1Jld
Genetic
Background
involves: 129P2/OlaHsd * Black Swiss * CF-1
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Fgatm1Jld mutation (0 available); any Fga mutation (44 available)
Plgtm1Jld mutation (2 available); any Plg mutation (5 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
mortality/aging
N
• show rescue from the early morbidity and premature death seen in single Plg homozygotes and show no signs of weight loss or wasting

homeostasis/metabolism
• shortly after birth, a small fraction of neonates show peritoneal bleeding from which they generally recover, indicating lack of clotting function
• exhibit distinctly larger deposits of dried blood at wound margins and scabs of wounds appear initially less stable than in controls and resumed bleeding is occasionally apparent
• exhibit distinctly larger deposits of dried blood at wound margins, however do not exhibit any of the wound healing defects seen in single Plg homozygotes
• scabs of wounds appear initially less stable than in controls and resume bleeding is occasionally apparent

liver/biliary system
• 6% (1 of 17) show hemorrhagic organized liver lesion
• 6% (1 of 17) show dystrophic calcification in liver
• 41% (7 of 17) show sporadic necrotic liver foci

immune system
N
• exhibit rescue of the various ulcerations and lesions seen in single Plg homozygotes

digestive/alimentary system
• 6% (1 of 17) show dystrophic calcification in duodenum


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
03/25/2025
MGI 6.24
The Jackson Laboratory