Slc16a3 | solute carrier family 16 (monocarboxylic acid transporters), member 3
Physiological systems
20 / 24 physiological systems tested
20 No significant impact
4 Not tested
Data collections
Gene metrics:0Significant phenotypes
0Associated diseases
Expression examined in:46Adult tissues
42Embryo tissues
Human diseases caused by Slc16a3 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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