Slc5a4a | solute carrier family 5, member 4a
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:0Adult tissues
0Embryo tissues
Human diseases caused by Slc5a4a 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
Loading...