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Symbol Name ID |
Slc26a1
solute carrier family 26 (sulfate transporter), member 1 MGI:2385894 |
| Darker colors indicate more annotations |
| Human Phenotypes | Hyperoxaluria |
| Disease(s) Associated with SLC26A1 | |
| calcium oxalate nephrolithiasis |
| Mouse Phenotypes | increased circulating calcium level |
hyposulfatemia |
increased circulating alanine transaminase level |
abnormal mineral level |
increased urine calcium level |
increased urine sulfate level |
increased physiological sensitivity to xenobiotic |
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| Availability | Mouse Genotype | |||||||
| Slc26a1tm1Mark/Slc26a1tm1Mark | ||||||||
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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