Slc25a24 | solute carrier family 25 (mitochondrial carrier, phosphate carrier), member 24

GeneMGI:1917160Synonyms: 2610016M12Rik

Physiological systems

18 / 24 physiological systems tested

3 Significantly impacted by the knock-out

 Vision/eye Behavior/neurological Cardiovascular system

15 No significant impact

6 Not tested

Gene metrics:3Significant phenotypes
3Associated diseases
Expression examined in:50Adult tissues
0Embryo tissues

Phenotypes

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* This parameter was manually assessed for significance.
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lacZ Expression

Associated images

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Human diseases caused by Slc25a24 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

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IMPC related publications

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Order Mouse and ES Cells

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