Tent5c | terminal nucleotidyltransferase 5C

GeneMGI:1921895Synonyms: 4930431B09Rik, Fam46c

Physiological systems

18 / 24 physiological systems tested

3 Significantly impacted by the knock-out

 Hematopoietic system Behavior/neurological Mortality/aging

15 No significant impact

6 Not tested

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

Phenotypes

increased grip strength2 supporting datasetsTent5ctm1b(KOMP)WtsiheterozygoteEarly adult7.92x10-5 
decreased mean corpuscular hemoglobin1 supporting datasetTent5ctm1b(KOMP)WtsiheterozygoteEarly adult2.39x10-7 
preweaning lethality, complete penetrance1 supporting datasetTent5ctm1b(KOMP)WtsihomozygoteEarly adultN/A * 
* 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% (0/2)0.7% (4/570)
aortaheterozygoten/a50% (1/2)0.19% (1/533)
blood vesselheterozygoten/a50% (1/2)0% (0/173)
boneheterozygoten/a50% (1/2)0% (0/394)
brainheterozygoten/a100% (2/2)0.86% (5/579)
brainstemheterozygoten/a100% (1/1)0.41% (2/490)
brown adipose tissueheterozygoten/a0% (0/2)0% (0/588)
cartilage tissueheterozygoten/a50% (1/2)0.22% (1/454)
cerebellumheterozygoten/a100% (1/1)0.56% (3/532)
cerebral cortexheterozygoten/a0% (0/2)0.41% (2/491)
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Human diseases caused by Tent5c 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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Tent5ctm1a(KOMP)WtsiKO first allele (reporter-tagged insertion with conditional potential)targeting vector
ES Cell
mouse
Tent5ctm1b(KOMP)WtsiReporter-tagged deletion allele (with selection cassette)mouse

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