Slc25a11 | solute carrier family 25 (mitochondrial carrier oxoglutarate carrier), member 11
Physiological systems
17 / 24 physiological systems tested
3 Significantly impacted by the knock-out
Nervous system Mortality/aging Embryo
14 No significant impact
7 Not tested
Data collections
Gene metrics:2Significant phenotypes
2Associated diseases
Expression examined in:0Adult tissues
0Embryo tissues
Human diseases caused by Slc25a11 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.
External links
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