Slc25a21 | solute carrier family 25 (mitochondrial oxodicarboxylate carrier), member 21
Physiological systems
20 / 24 physiological systems tested
7 Significantly impacted by the knock-out
Behavior/neurological Homeostasis/metabolism Adipose tissue Skeleton Hematopoietic system Craniofacial Growth/size/body region
13 No significant impact
4 Not tested
Data collections
Gene metrics:16Significant phenotypes
1Associated diseases
Expression examined in:90Adult tissues
0Embryo tissues
Human diseases caused by Slc25a21 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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