Snorc | secondary ossification center associated regulator of chondrocyte maturation
Physiological systems
11 / 24 physiological systems tested
11 No significant impact
13 Not tested
Data collections
Gene metrics:0Significant phenotypes
0Associated diseases
Expression examined in:50Adult tissues
0Embryo tissues
adrenal gland | heterozygote | n/a | 0% (0/1) | 0.7% (4/570) |
aorta | heterozygote | n/a | 0% (0/1) | 0.19% (1/533) |
bone | heterozygote | n/a | 0% (0/1) | 0% (0/394) |
brain | heterozygote | n/a | 0% (0/1) | 0.86% (5/579) |
brainstem | heterozygote | n/a | 0% (0/1) | 0.41% (2/490) |
brown adipose tissue | heterozygote | n/a | 0% (0/1) | 0% (0/588) |
cartilage tissue | heterozygote | Wholemount images | 100% (1/1) | 0.22% (1/454) |
cerebellum | heterozygote | n/a | 0% (0/1) | 0.56% (3/532) |
cerebral cortex | heterozygote | n/a | 0% (0/1) | 0.41% (2/491) |
esophagus | heterozygote | n/a | 0% (0/1) | 1.67% (7/419) |
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.
External links
No external links available for Snorc.
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Snorctm1a(EUCOMM)Hmgu | KO first allele (reporter-tagged insertion with conditional potential) | | targeting vector ES Cell mouse |
Snorctm1b(EUCOMM)Hmgu | Reporter-tagged deletion allele (with selection cassette) | | mouse |
Snorctm1e(EUCOMM)Hmgu | Targeted, non-conditional allele | | ES Cell |