Xrcc3 | X-ray repair complementing defective repair in Chinese hamster cells 3

GeneMGI:1921585Synonyms: 4432412E01Rik

Physiological systems

19 / 24 physiological systems tested

2 Significantly impacted by the knock-out

 Hematopoietic system Mortality/aging

17 No significant impact

5 Not tested

Gene metrics:3Significant phenotypes
2Associated diseases
Expression examined in:52Adult tissues
26Embryo tissues

Phenotypes

embryonic lethality prior to tooth bud stage1 supporting datasetXrcc3tm1b(KOMP)MbphomozygoteE12.5N/A * 
preweaning lethality, complete penetrance1 supporting datasetXrcc3tm1b(KOMP)MbphomozygoteEarly adultN/A * 
decreased mean corpuscular volume1 supporting datasetXrcc3tm1b(KOMP)MbpheterozygoteEarly adult1.13x10-5 
* Does not have a P-value assigned because it was manually marked as significant.
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* This parameter was manually assessed for significance.
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lacZ Expression

adrenal glandheterozygoteSection images
100% (2/2)0.7% (4/570)
aortaheterozygoten/a0% (0/2)0.19% (1/533)
boneheterozygoten/a0% (0/2)0% (0/394)
bone marrowheterozygoten/a0% (0/2)0% (0/22)
brainheterozygoteSection images
100% (2/2)0.86% (5/579)
brainstemheterozygoteSection images
100% (2/2)0.41% (2/490)
brown adipose tissueheterozygoteSection images
100% (2/2)0% (0/588)
cartilage tissueheterozygoten/a0% (0/2)0.22% (1/454)
cerebellumheterozygoten/a0% (0/2)0.56% (3/532)
cerebral cortexheterozygoten/a0% (0/2)0.41% (2/491)
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Human diseases caused by Xrcc3 mutations

The analysis uses data from IMPC, along with published data on other mouse mutants, in comparison to human disease reports in OMIM, Orphanet, and DECIPHER.

Phenotype comparisons summarize the similarity of mouse phenotypes with human disease phenotypes.






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Histopathology

IMPC related publications

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Xrcc3tm1a(KOMP)MbpKO first allele (reporter-tagged insertion with conditional potential)targeting vector
ES Cell
mouse
Xrcc3tm1b(KOMP)MbpReporter-tagged deletion allele (with selection cassette)mouse
Xrcc3tm1e(KOMP)MbpTargeted, non-conditional alleleES Cell

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