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 09/03/2024 MGI 6.24 |
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