Slc22a8 | solute carrier family 22 (organic anion transporter), member 8
Physiological systems
19 / 24 physiological systems tested
1 Significantly impacted by the knock-out
Homeostasis/metabolism
18 No significant impact
5 Not tested
Data collections
Gene metrics:1Significant phenotypes
0Associated diseases
Expression examined in:46Adult tissues
42Embryo tissues
Human diseases caused by Slc22a8 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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