Akap7 | A kinase anchor protein 7

GeneMGI:1859150Synonyms: Akap18, AKAP15

Physiological systems

16 / 24 physiological systems tested

1 Significantly impacted by the knock-out

 Skeleton

15 No significant impact

8 Not tested

Gene metrics:1Significant phenotypes
0Associated diseases
Expression examined in:51Adult tissues
0Embryo tissues

Phenotypes

decreased bone mineral density1 supporting datasetAkap7tm2b(EUCOMM)HmguhomozygoteEarly adult5.69x10-5 
* 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 glandheterozygoteWholemount images
100% (2/2)0.7% (4/570)
aortaheterozygoten/a0% (0/2)0.19% (1/533)
boneheterozygoteWholemount images
100% (2/2)0% (0/394)
brainheterozygoteWholemount images
100% (2/2)0.86% (5/579)
brainstemheterozygoten/a0% (0/2)0.41% (2/490)
brown adipose tissueheterozygoten/a0% (0/2)0% (0/588)
cartilage tissueheterozygoteWholemount images
100% (2/2)0.22% (1/454)
cecumheterozygoten/a0% (0/1)7.75% (22/284)
cerebellumheterozygoten/a0% (0/2)0.56% (3/532)
cerebral cortexheterozygoten/a0% (0/2)0.41% (2/491)
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Human diseases caused by Akap7 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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Akap7tm2a(EUCOMM)HmguKO first allele (reporter-tagged insertion with conditional potential)targeting vector
ES Cell
mouse
Akap7tm2b(EUCOMM)HmguReporter-tagged deletion allele (with selection cassette)mouse
Akap7tm2e(EUCOMM)HmguTargeted, non-conditional alleleES Cell

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