Slc9a7 | solute carrier family 9 (sodium/hydrogen exchanger), member 7
Physiological systems
15 / 24 physiological systems tested
15 No significant impact
9 Not tested
Data collections
Gene metrics:0Significant phenotypes
2Associated diseases
Expression examined in:0Adult tissues
0Embryo tissues
Human diseases caused by Slc9a7 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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