Snorc | secondary ossification center associated regulator of chondrocyte maturation

GeneMGI:1920484Synonyms: 3110079O15Rik, Snorc

Physiological systems

11 / 24 physiological systems tested

11 No significant impact

13 Not tested

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

Phenotypes

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* This parameter was manually assessed for significance.
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lacZ Expression

adrenal glandheterozygoten/a0% (0/1)0.7% (4/570)
aortaheterozygoten/a0% (0/1)0.19% (1/533)
boneheterozygoten/a0% (0/1)0% (0/394)
brainheterozygoten/a0% (0/1)0.86% (5/579)
brainstemheterozygoten/a0% (0/1)0.41% (2/490)
brown adipose tissueheterozygoten/a0% (0/1)0% (0/588)
cartilage tissueheterozygoteWholemount images
100% (1/1)0.22% (1/454)
cerebellumheterozygoten/a0% (0/1)0.56% (3/532)
cerebral cortexheterozygoten/a0% (0/1)0.41% (2/491)
esophagusheterozygoten/a0% (0/1)1.67% (7/419)
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Human diseases caused by Snorc 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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Order Mouse and ES Cells

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Snorctm1a(EUCOMM)HmguKO first allele (reporter-tagged insertion with conditional potential)targeting vector
ES Cell
mouse
Snorctm1b(EUCOMM)HmguReporter-tagged deletion allele (with selection cassette)mouse
Snorctm1e(EUCOMM)HmguTargeted, non-conditional alleleES Cell

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