Hemgn | hemogen

GeneMGI:2136910Synonyms: 4921524M03Rik, EDAG

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:50Adult tissues
46Embryo tissues

Phenotypes

decreased mean corpuscular volume1 supporting datasetHemgntm1.1(KOMP)VlcghomozygoteEarly adult2.47x10-5 
decreased mean corpuscular hemoglobin1 supporting datasetHemgntm1.1(KOMP)VlcghomozygoteEarly adult6.01x10-7 
* 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 glandheterozygoteSection images
100% (2/2)0.7% (4/570)
aortaheterozygoteSection images
100% (2/2)0.19% (1/533)
bloodheterozygoteSection images
100% (2/2)0% (0/17)
bone marrowheterozygoteSection images
100% (2/2)0% (0/22)
brainheterozygoteSection images
100% (2/2)0.86% (5/579)
brainstemheterozygoteSection images
100% (2/2)0.41% (2/490)
brown adipose tissueheterozygoteSection images
100% (2/2)0% (0/588)
cartilage tissueheterozygoten/a0% (0/2)0.22% (1/454)
cerebellumheterozygoteSection images
100% (2/2)0.56% (3/532)
cerebral cortexheterozygoteSection images
100% (2/2)0.41% (2/491)
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Human diseases caused by Hemgn 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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Hemgntm1(KOMP)VlcgReporter-tagged deletion allele (with selection cassette)ES Cell
mouse
Hemgntm1.1(KOMP)VlcgReporter-tagged deletion allele (post Cre, with no selection cassette)mouse
Hemgntm384(L1L2_gt1)KO first allele (reporter-tagged insertion with conditional potential)targeting vector

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