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Symbol Name ID |
Slc51a
solute carrier family 51, alpha subunit MGI:2146634 |
| Darker colors indicate more annotations |
| Human Phenotypes | Splenomegaly |
Hepatomegaly |
Short stature |
Failure to thrive |
| Disease(s) Associated with SLC51A | ||||
| progressive familial intrahepatic cholestasis |
| Mouse Phenotypes | postnatal growth retardation |
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| Availability | Mouse Genotype | |
| Slc51atm1Nbal/Slc51atm1Nbal | ||
| Slc51atm1Pda/Slc51atm1Pda | ||
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 05/28/2024 MGI 6.13 |
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