Pgs1 | phosphatidylglycerophosphate synthase 1

GeneMGI:1921701Synonyms: 2610019F11Rik, 4933424M23Rik

Physiological systems

18 / 24 physiological systems tested

2 Significantly impacted by the knock-out

 Homeostasis/metabolism Mortality/aging

16 No significant impact

6 Not tested

Gene metrics:2Significant phenotypes
0Associated diseases
Expression examined in:70Adult tissues
0Embryo tissues

Phenotypes

increased circulating phosphate level1 supporting datasetPgs1tm1b(EUCOMM)HmguheterozygoteEarly adult3.4x10-5 
preweaning lethality, complete penetrance1 supporting datasetPgs1tm1b(EUCOMM)HmguhomozygoteEarly adultN/A * 
* 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)
bloodheterozygoten/a0% (0/2)0% (0/17)
boneheterozygoten/a0% (0/2)0% (0/394)
bone marrowheterozygoten/a0% (0/2)0% (0/22)
brainheterozygoten/a0% (0/2)0.86% (5/579)
brainstemheterozygoten/a0% (0/2)0.41% (2/490)
brown adipose tissueheterozygoteWholemount images
50% (1/2)0% (0/588)
cartilage tissueheterozygoten/a0% (0/2)0.22% (1/454)
cecumheterozygoteWholemount images
0% (0/2)7.75% (22/284)
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Human diseases caused by Pgs1 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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Pgs1tm1a(EUCOMM)HmguKO first allele (reporter-tagged insertion with conditional potential)targeting vector
ES Cell
mouse
Pgs1tm1b(EUCOMM)HmguReporter-tagged deletion allele (with selection cassette)mouse
Pgs1tm1e(EUCOMM)HmguTargeted, non-conditional alleleES Cell

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