Serpinb5 | serine (or cysteine) peptidase inhibitor, clade B, member 5

GeneMGI:109579Synonyms: Spi7, ovalbumin, +2 more

Physiological systems

18 / 24 physiological systems tested

2 Significantly impacted by the knock-out

 Homeostasis/metabolism Behavior/neurological

16 No significant impact

6 Not tested

Gene metrics:3Significant phenotypes
0Associated diseases
Expression examined in:48Adult tissues
50Embryo tissues

Phenotypes

increased circulating cholesterol level1 supporting datasetSerpinb5tm1b(KOMP)WtsihomozygoteEarly adult1.06x10-7 
impaired righting response1 supporting datasetSerpinb5tm1b(KOMP)WtsihomozygoteEarly adult3.49x10-6 
abnormal sleep behavior1 supporting datasetSerpinb5tm1b(KOMP)WtsihomozygoteEarly adult1.6x10-5 
* 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% (0/2)0.7% (4/570)
aortaheterozygoten/a0% (0/2)0.19% (1/533)
brainheterozygoten/a0% (0/2)0.86% (5/579)
brainstemheterozygoten/a0% (0/2)0.41% (2/490)
brown adipose tissueheterozygoten/a0% (0/2)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)
epididymisheterozygoteSection images
100% (1/1)87.5% (21/24)
esophagusheterozygoteSection images
100% (2/2)1.67% (7/419)
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Human diseases caused by Serpinb5 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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Serpinb5tm1a(KOMP)WtsiKO first allele (reporter-tagged insertion with conditional potential)targeting vector
ES Cell
mouse
Serpinb5tm1b(KOMP)WtsiReporter-tagged deletion allele (with selection cassette)mouse
Serpinb5tm1e(KOMP)WtsiTargeted, non-conditional alleleES Cell

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