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Symbol Name ID |
Slc26a2
solute carrier family 26 (sulfate transporter), member 2 MGI:892977 |
| Darker colors indicate more annotations |
| Human Phenotypes | Edema |
Hydrops fetalis |
Costal cartilage calcification |
| Disease(s) Associated with SLC26A2 | |||
| achondrogenesis type IB | |||
| diastrophic dysplasia |
| Mouse Phenotypes | impaired glucose tolerance |
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| Availability | Mouse Genotype | |
| Slc26a2em1(IMPC)Bay/Slc26a2+ | ||
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 04/09/2024 MGI 6.23 |
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