Slc17a3 | solute carrier family 17 (sodium phosphate), member 3
Physiological systems
20 / 24 physiological systems tested
20 No significant impact
4 Not tested
Data collections
Gene metrics:0Significant phenotypes
1Associated diseases
Expression examined in:0Adult tissues
42Embryo tissues
Human diseases caused by Slc17a3 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 Slc17a3.
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| Slc17a3tm1a(KOMP)Wtsi | KO first allele (reporter-tagged insertion with conditional potential) | | targeting vector ES Cell |
| Slc17a3tm1e(KOMP)Wtsi | Targeted, non-conditional allele | | ES Cell |
| Slc17a3tm2a(KOMP)Wtsi | KO first allele (reporter-tagged insertion with conditional potential) | | targeting vector ES Cell mouse |
| Slc17a3tm2b(KOMP)Wtsi | Reporter-tagged deletion allele (with selection cassette) | | mouse |
| Slc17a3tm2e(KOMP)Wtsi | Targeted, non-conditional allele | | ES Cell |
| Slc17a3tm41305(L1L2_gt1) | KO first allele (reporter-tagged insertion with conditional potential) | | targeting vector |