|
Symbol Name ID |
Slc12a1
solute carrier family 12, member 1 MGI:103150 |
| Darker colors indicate more annotations |
| Human Phenotypes | Chondrocalcinosis |
Osteopenia |
| Disease(s) Associated with SLC12A1 | ||
| Bartter disease type 1 |
| Mouse Phenotypes | abnormal bone structure |
decreased bone mineral density |
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| Availability | Mouse Genotype | ||
| Slc12a1urehr3/Slc12a1urehr3 | |||
Mouse Genome Database (MGD), Gene Expression Database (GXD), Mouse Models of Human Cancer database (MMHCdb) (formerly Mouse Tumor Biology (MTB)), Gene Ontology (GO) |
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last database update 04/16/2024 MGI 6.23 |
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