Tpcn2 | two pore segment channel 2

GeneMGI:2385297Synonyms: D830047E22Rik

Physiological systems

22 / 24 physiological systems tested

4 Significantly impacted by the knock-out

 Homeostasis/metabolism Immune system Hematopoietic system Behavior/neurological

18 No significant impact

2 Not tested

Gene metrics:5Significant phenotypes
1Associated diseases
Expression examined in:46Adult tissues
42Embryo tissues

Phenotypes

increased eosinophil cell number1 supporting datasetTpcn2tm1b(EUCOMM)HmguhomozygoteEarly adult8.97x10-5 
abnormal vocalization1 supporting datasetTpcn2Gt(YHD437)ByghomozygoteEarly adult5.1x10-6 
increased circulating triglyceride level1 supporting datasetTpcn2tm1b(EUCOMM)HmguhomozygoteEarly adult1.36x10-5 
abnormal behavior2 supporting datasetsTpcn2Gt(YHD437)ByghomozygoteEarly adult4.81x10-6 
decreased circulating sodium level1 supporting datasetTpcn2Gt(YHD437)ByghomozygoteEarly adult3.08x10-5 
* 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/a100% (8/8)0.7% (4/570)
aortaheterozygoten/a100% (4/4)0.19% (1/533)
boneheterozygoten/a100% (8/8)0% (0/394)
brainheterozygoten/a100% (8/8)0.86% (5/579)
brainstemheterozygoten/a100% (8/8)0.41% (2/490)
brown adipose tissueheterozygoten/a0% (0/8)0% (0/588)
cartilage tissueheterozygoten/a100% (8/8)0.22% (1/454)
cerebellumheterozygoten/a100% (8/8)0.56% (3/532)
cerebral cortexheterozygoten/a28.57% (2/7)0.41% (2/491)
esophagusheterozygoten/a0% (0/8)1.67% (7/419)
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Human diseases caused by Tpcn2 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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Tpcn2tm1a(EUCOMM)HmguKO first allele (reporter-tagged insertion with conditional potential)targeting vector
ES Cell
mouse
Tpcn2tm1b(EUCOMM)HmguReporter-tagged deletion allele (with selection cassette)mouse
Tpcn2tm1c(EUCOMM)HmguWild type floxed exon (post-Flp)mouse
Tpcn2tm1e(EUCOMM)HmguTargeted, non-conditional alleleES Cell

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