Tatdn3 | TatD DNase domain containing 3

GeneMGI:1916222Synonyms: 1500010M24Rik

Physiological systems

18 / 24 physiological systems tested

3 Significantly impacted by the knock-out

 Homeostasis/metabolism Adipose tissue Skeleton

15 No significant impact

6 Not tested

Gene metrics:3Significant phenotypes
0Associated diseases
Expression examined in:45Adult tissues
0Embryo tissues

Phenotypes

decreased blood urea nitrogen level1 supporting datasetTatdn3tm1a(EUCOMM)WtsihomozygoteEarly adult1.49x10-5 
increased total body fat amount1 supporting datasetTatdn3tm1b(EUCOMM)WtsihomozygoteEarly adult7.86x10-5 
decreased bone mineral density1 supporting datasetTatdn3tm1b(EUCOMM)WtsihomozygoteEarly adult8.57x10-5 
* 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 glandheterozygoten/a0% (0/4)0.7% (4/570)
aortaheterozygoten/a50% (2/4)0.19% (1/533)
blood vesselheterozygoten/a0% (0/4)0% (0/173)
boneheterozygoten/a0% (0/4)0% (0/394)
brainheterozygoten/a100% (4/4)0.86% (5/579)
brainstemheterozygoten/a0% (0/4)0.41% (2/490)
brown adipose tissueheterozygoten/a0% (0/4)0% (0/588)
cartilage tissueheterozygoten/a0% (0/4)0.22% (1/454)
cerebellumheterozygoten/a0% (0/4)0.56% (3/532)
cerebral cortexheterozygoten/a0% (0/4)0.41% (2/491)
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Human diseases caused by Tatdn3 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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Tatdn3tm1a(EUCOMM)WtsiKO first allele (reporter-tagged insertion with conditional potential)targeting vector
ES Cell
mouse
Tatdn3tm1b(EUCOMM)WtsiReporter-tagged deletion allele (with selection cassette)mouse
Tatdn3tm1e(EUCOMM)WtsiTargeted, non-conditional alleleES Cell

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