Slc25a44 | solute carrier family 25, member 44
Physiological systems
17 / 24 physiological systems tested
1 Significantly impacted by the knock-out
Behavior/neurological
16 No significant impact
7 Not tested
Data collections
Gene metrics:2Significant phenotypes
0Associated diseases
Expression examined in:0Adult tissues
0Embryo tissues
Human diseases caused by Slc25a44 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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