Mecr | mitochondrial trans-2-enoyl-CoA reductase

GeneMGI:1349441Synonyms: Nrbf1

Physiological systems

19 / 24 physiological systems tested

2 Significantly impacted by the knock-out

 Behavior/neurological Mortality/aging

17 No significant impact

5 Not tested

Data collections

Viability data
Body weight measurements
Embryo imaging data
Gene metrics:3Significant phenotypes
3Associated diseases
Expression examined in:45Adult tissues
0Embryo tissues

Phenotypes

abnormal response to tactile stimuli1 supporting datasetMecrtm1a(EUCOMM)WtsiheterozygoteEarly adult6.64x10-5 
preweaning lethality, complete penetrance1 supporting datasetMecrtm1a(EUCOMM)WtsihomozygoteEarly adultN/A * 
abnormal gait1 supporting datasetMecrtm1a(EUCOMM)WtsiheterozygoteEarly adult2.48x10-5 
* 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 glandheterozygoten/a0% (0/2)0.7% (4/570)
aortaheterozygoten/an/a0.19% (1/533)
blood vesselheterozygoten/a0% (0/2)0% (0/173)
boneheterozygoten/a0% (0/2)0% (0/394)
brainheterozygoten/a100% (2/2)0.86% (5/579)
brainstemheterozygoten/an/a0.41% (2/490)
brown adipose tissueheterozygoten/a0% (0/2)0% (0/588)
cartilage tissueheterozygoten/a0% (0/2)0.22% (1/454)
cerebellumheterozygoten/an/a0.56% (3/532)
cerebral cortexheterozygoten/an/a0.41% (2/491)
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Associated images

Human diseases caused by Mecr 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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Mecrtm1a(EUCOMM)WtsiKO first allele (reporter-tagged insertion with conditional potential)targeting vector
ES Cell
mouse
Mecrtm2a(EUCOMM)WtsiKO first allele (reporter-tagged insertion with conditional potential)targeting vector
ES Cell
Mecrtm2e(EUCOMM)WtsiTargeted, non-conditional alleleES Cell

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