C1qtnf7 | C1q and tumor necrosis factor related protein 7
Physiological systems
18 / 24 physiological systems tested
18 No significant impact
6 Not tested
Data collections
Gene metrics:0Significant phenotypes
0Associated diseases
Expression examined in:73Adult tissues
0Embryo tissues
| adrenal gland | heterozygote | Wholemount images | 50% (2/4) | 0.7% (4/570) |
| aorta | heterozygote | Wholemount images | 100% (2/2) | 0.19% (1/533) |
| blood | heterozygote | n/a | 0% (0/2) | 0% (0/17) |
| bone marrow | heterozygote | n/a | 0% (0/2) | 0% (0/22) |
| brain | heterozygote | Wholemount images | 75% (3/4) | 0.86% (5/579) |
| brainstem | heterozygote | n/a | n/a | 0.41% (2/490) |
| brown adipose tissue | heterozygote | n/a | 0% (0/3) | 0% (0/588) |
| cartilage tissue | heterozygote | n/a | n/a | 0.22% (1/454) |
| cecum | heterozygote | n/a | 50% (2/4) | 7.75% (22/284) |
| cerebellum | heterozygote | Wholemount images | 50% (2/4) | 0.56% (3/532) |
Human diseases caused by C1qtnf7 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 C1qtnf7.
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| C1qtnf7tm1(KOMP)Vlcg | Reporter-tagged deletion allele (with selection cassette) | | ES Cell mouse |
| C1qtnf7tm1.1(KOMP)Vlcg | Reporter-tagged deletion allele (post Cre, with no selection cassette) | | mouse |
| C1qtnf7tm106107(L1L2_Bact_P) | KO first allele (reporter-tagged insertion with conditional potential) | | targeting vector |