Slc39a7 | solute carrier family 39 (zinc transporter), member 7
Physiological systems
22 / 24 physiological systems tested
1 Significantly impacted by the knock-out
Mortality/aging
21 No significant impact
2 Not tested
Data collections
Gene metrics:3Significant phenotypes
2Associated diseases
Expression examined in:73Adult tissues
29Embryo tissues
Human diseases caused by Slc39a7 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
No external links available for Slc39a7.