|
Symbol Name ID |
Micu1
mitochondrial calcium uptake 1 MGI:2384909 |
| Darker colors indicate more annotations |
| Human Phenotypes | Calf muscle hypertrophy |
Progressive extrapyramidal muscular rigidity |
Hypotonia |
Difficulty running |
Difficulty walking |
Easy fatigability |
Frequent falls |
Muscle spasm |
Proximal muscle weakness |
Gowers sign |
Increased variability in muscle fiber diameter |
Central core regions in muscle fibers |
Centrally nucleated skeletal muscle fibers |
| Disease(s) Associated with MICU1 | |||||||||||||
| myopathy with extrapyramidal signs |
| Mouse Phenotypes | decreased skeletal muscle fiber number |
abnormal muscle physiology |
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| Availability | Mouse Genotype | ||
| Micu1em#Fink/Micu1em#Fink | |||
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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