Gpr183 | G protein-coupled receptor 183

GeneMGI:2442034Synonyms: Ebi2

Physiological systems

18 / 24 physiological systems tested

1 Significantly impacted by the knock-out

 Hematopoietic system

17 No significant impact

6 Not tested

Gene metrics:2Significant phenotypes
0Associated diseases
Expression examined in:48Adult tissues
50Embryo tissues

Phenotypes

increased erythrocyte cell number1 supporting datasetGpr183tm1.1(KOMP)VlcghomozygoteEarly adult1.33x10-5 
increased hematocrit1 supporting datasetGpr183tm1.1(KOMP)VlcghomozygoteEarly adult7.07x10-7 
* 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)
brainheterozygoteSection images
100% (2/2)0.86% (5/579)
brainstemheterozygoteSection images
100% (2/2)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 cortexheterozygoteSection images
100% (2/2)0.41% (2/491)
epididymisheterozygoten/a0% (0/1)87.5% (21/24)
esophagusheterozygoten/a0% (0/2)1.67% (7/419)
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Human diseases caused by Gpr183 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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Gpr183tm1(KOMP)VlcgReporter-tagged deletion allele (with selection cassette)ES Cell
mouse
Gpr183tm1.1(KOMP)VlcgReporter-tagged deletion allele (post Cre, with no selection cassette)mouse
Gpr183tm1a(EUCOMM)HmguKO first allele (reporter-tagged insertion with conditional potential)targeting vector
ES Cell
Gpr183tm1e(EUCOMM)HmguTargeted, non-conditional alleleES Cell

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