Tnpo2 | transportin 2 (importin 3, karyopherin beta 2b)

GeneMGI:2384849Synonyms: Kpnb2b, TRN2, +1 more

Physiological systems

12 / 24 physiological systems tested

12 No significant impact

12 Not tested

Gene metrics:0Significant phenotypes
1Associated diseases
Expression examined in:51Adult tissues
0Embryo tissues

Phenotypes

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* This parameter was manually assessed for significance.
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lacZ Expression

adrenal glandheterozygoteWholemount images
100% (2/2)0.7% (4/570)
aortaheterozygoteWholemount images
100% (2/2)0.19% (1/533)
boneheterozygoteWholemount images
100% (2/2)0% (0/394)
brainheterozygoteWholemount images
100% (2/2)0.86% (5/579)
brainstemheterozygoteWholemount images
100% (2/2)0.41% (2/490)
brown adipose tissueheterozygoten/a0% (0/2)0% (0/588)
cartilage tissueheterozygoteWholemount images
100% (2/2)0.22% (1/454)
cecumheterozygoten/a0% (0/2)7.75% (22/284)
cerebellumheterozygoteWholemount images
100% (2/2)0.56% (3/532)
cerebral cortexheterozygoteWholemount images
100% (2/2)0.41% (2/491)
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Human diseases caused by Tnpo2 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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Tnpo2tm1a(EUCOMM)HmguKO first allele (reporter-tagged insertion with conditional potential)targeting vector
ES Cell
mouse
Tnpo2tm1b(EUCOMM)HmguReporter-tagged deletion allele (with selection cassette)mouse
Tnpo2tm1e(EUCOMM)HmguTargeted, non-conditional alleleES Cell

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