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Phenotypes associated with this allele
Allele Symbol
Allele Name
Allele ID
Fdxrtm1Xch
targeted mutation 1, Xinbin Chen
MGI:6115883
Summary 4 genotypes
Jump to Allelic Composition Genetic Background Genotype ID
hm1
Fdxrtm1Xch/Fdxrtm1Xch B6.Cg-Fdxrtm1Xch MGI:6715097
ht2
Fdxrtm1Xch/Fdxr+ B6.Cg-Fdxrtm1Xch MGI:6715101
cx3
Fdxrtm1Xch/Fdxr+
Trp53tm1Tyj/Trp53+
involves: 129S2/SvPas * C57BL/6 MGI:6715104
cx4
Fdxrtm1Xch/Fdxr+
Trp53tm1Tyj/Trp53tm1Tyj
involves: 129S2/SvPas * C57BL/6 MGI:6715105


Genotype
MGI:6715097
hm1
Allelic
Composition
Fdxrtm1Xch/Fdxrtm1Xch
Genetic
Background
B6.Cg-Fdxrtm1Xch
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Fdxrtm1Xch mutation (0 available); any Fdxr mutation (22 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
mortality/aging
• homozygotes are alive at E7.0-E8.0 but resorbed at E8.5-E9.0; no live mice are born from heterozygous intercrosses
• embryonic lethality is likely due to iron overload

embryo
• E8.0 embryos exhibit severe developmental defects
• E7.5 embryos fail to develop normal layers of embryonic tissues
• failure to develop normal embryonic ectoderm
• failure to develop normal mesoderm
• E7.5 embryos fail to develop normal layers of extraembryonic tissues
• failure to develop normal extraembryonic ectoderm
• failure to develop normal extraembryonic visceral endoderm
• failure to develop normal visceral endoderm

homeostasis/metabolism
• Pearl's Prussian blue staining revealed extensive iron overload in E8.0 embryos




Genotype
MGI:6715101
ht2
Allelic
Composition
Fdxrtm1Xch/Fdxr+
Genetic
Background
B6.Cg-Fdxrtm1Xch
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Fdxrtm1Xch mutation (0 available); any Fdxr mutation (22 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
mortality/aging
• although heterozygores appear healthy with no obvious abnormalities during the first 6 months of life, median survival is significantly shorter than that for wild-type controls (102 weeks versus 117 weeks)

neoplasm
• heterozygotes are prone to a wide spectrum of spontaneous tumors; 89.7% of mice develop tumors versus 22.2% of wild-type controls
• 11 of 29 mice develop liver tumors
• liver tumor tissue shows increased transcript levels of alpha-fetoprotein (a hepatocellular carcinoma biomarker) as well as decreased reticulin staining along with widened trabeculae, encompassing 3 or more cell layers
• however, RT-PCR analysis revealed no mutation in the p53 DNA-binding domain
• 2 of 11 liver tumors are hepatocellular carcinomas (HCCs)
• 3 of 29 mice develop hemangiomas
• 19 of 29 mice develop high-grade lymphomas
• 5 of 29 mice develop T-cell lymphomas
• 12 of 29 mice develop B-cell lymphomas
• 4 of 29 mice develop lung carcinomas
• 7 of 29 mice develop high-grade malignant sarcomas
• 3 of 29 mice develop angiosarcomas
• 2 of 29 mice develop myeloid sarcomas
• 1 of 29 mice develop plasmacytomas

homeostasis/metabolism
• liver tissues and mouse embryonic fibroblasts (MEFs) show increased protein expression of IREB2 (iron responsive element binding protein 2; aka IRP2) and TFRC (transferrin receptor; aka TfR1) but reduced expression of ACO1 (aconitase 1; aka IRP1) and FTH1 (ferritin heavy polypeptide 1)
• Pearl's Prussian blue staining revealed moderate iron accumulation in E8.0 embryos
• a QuantiChrom iron assay showed an increased iron level in the mitochondria but not in the cytoplasm of heterozygous MEFs
• Pearl's Prussian blue staining revealed extensive iron accumulation in hepatocytes
• liver tissues and MEFs show reduced protein levels of tumor protein p53 and CDKN1A (aka p21)
• however, RT-PCR showed that Trp53 mRNA levels in MEFs are normal
• liver tumor tissue shows increased transcript levels of alpha-fetoprotein (a hepatocellular carcinoma biomarker)

liver/biliary system
• Pearl's Prussian blue staining revealed extensive iron accumulation in hepatocytes
• 10 of 29 mice exhibit chronic hepatitis
• 15 of 29 mice exhibit liver steatosis
• 11 of 29 mice develop liver tumors
• liver tumor tissue shows increased transcript levels of alpha-fetoprotein (a hepatocellular carcinoma biomarker) as well as decreased reticulin staining along with widened trabeculae, encompassing 3 or more cell layers
• however, RT-PCR analysis revealed no mutation in the p53 DNA-binding domain
• 2 of 11 liver tumors are hepatocellular carcinomas (HCCs)

cellular
• MEFs show mitochondrial iron accumulation
• RSL3- and erastin-induced ferroptosis is inhibited in MEFs
• MEFs show increased proliferation over a 6-d period

immune system
• 10 of 29 mice exhibit chronic hepatitis

endocrine/exocrine glands
• 5 of 29 mice develop T-cell lymphomas

respiratory system
• 4 of 29 mice develop lung carcinomas




Genotype
MGI:6715104
cx3
Allelic
Composition
Fdxrtm1Xch/Fdxr+
Trp53tm1Tyj/Trp53+
Genetic
Background
involves: 129S2/SvPas * C57BL/6
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Fdxrtm1Xch mutation (0 available); any Fdxr mutation (22 available)
Trp53tm1Tyj mutation (12 available); any Trp53 mutation (232 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
homeostasis/metabolism
• mild iron overload in E8.0 embryos




Genotype
MGI:6715105
cx4
Allelic
Composition
Fdxrtm1Xch/Fdxr+
Trp53tm1Tyj/Trp53tm1Tyj
Genetic
Background
involves: 129S2/SvPas * C57BL/6
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Fdxrtm1Xch mutation (0 available); any Fdxr mutation (22 available)
Trp53tm1Tyj mutation (12 available); any Trp53 mutation (232 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
homeostasis/metabolism
• mild iron overload in E8.0 embryos





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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