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Symbol Name ID |
Ryr3
ryanodine receptor 3 MGI:99684 |
| Darker colors indicate more annotations |
| Human Phenotypes | Frequent falls |
Delayed speech and language development |
Global developmental delay |
Delayed ability to walk |
Seizure |
| Disease(s) Associated with RYR3 | |||||
| congenital myopathy 20 |
| Mouse Phenotypes | enhanced long-term potentiation |
absent long-term depression |
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| Availability | Mouse Genotype | ||
| Ryr3tm1Jms/Ryr3tm1Jms | |||
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 04/23/2024 MGI 6.23 |
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