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Symbol Name ID |
Slc30a10
solute carrier family 30, member 10 MGI:2685058 |
| * | Aspects of the system are reported to show a normal phenotype. |
| Darker colors indicate more annotations |
| Human Phenotypes | Spastic paraparesis |
Poor fine motor coordination |
Abnormality of extrapyramidal motor function |
Bradykinesia |
Parkinsonism |
Tremor |
Dysarthria |
Dystonia |
Steppage gait |
Postural instability |
Sensorimotor neuropathy |
| Disease(s) Associated with SLC30A10 | |||||||||||
| hypermanganesemia with dystonia 1 |
| Mouse Phenotypes | nervous system phenotype |
increased brain iron level |
increased brain manganese level |
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| Availability | Mouse Genotype | |||
| Slc30a10tm1.1Sommu/Slc30a10tm1.1Sommu | * | |||
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 05/14/2024 MGI 6.23 |
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