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Symbol Name ID |
Ryr3
ryanodine receptor 3 MGI:99684 |
| Darker colors indicate more annotations |
| Human Phenotypes | Weakness of facial musculature |
Scapular winging |
Congenital contracture |
Elbow contracture |
Difficulty climbing stairs |
Difficulty running |
Frequent falls |
Proximal muscle weakness |
Gowers sign |
Type 1 muscle fiber predominance |
Increased variability in muscle fiber diameter |
Centrally nucleated skeletal muscle fibers |
Nemaline bodies |
Skeletal muscle atrophy |
| Disease(s) Associated with RYR3 | ||||||||||||||
| congenital myopathy 20 |
| Mouse Phenotypes | abnormal muscle contractility |
impaired muscle contractility |
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| Availability | Mouse Genotype | ||
| Ryr3tm1Vso/Ryr3tm1Vso | |||
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 04/16/2024 MGI 6.23 |
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