Slc23a4 | solute carrier family 23 member 4
Physiological systems
19 / 24 physiological systems tested
1 Significantly impacted by the knock-out
Renal/urinary system
18 No significant impact
5 Not tested
Data collections
Gene metrics:1Significant phenotypes
0Associated diseases
Expression examined in:45Adult tissues
0Embryo tissues
Human diseases caused by Slc23a4 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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