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Symbol Name ID |
Scyl1
SCY1-like 1 (S. cerevisiae) MGI:1931787 |
| * | Aspects of the system are reported to show a normal phenotype. |
| Darker colors indicate more annotations |
| Human Phenotypes | Distal lower limb muscle weakness |
Spasticity |
Frequent falls |
Generalized limb muscle atrophy |
| Disease(s) Associated with SCYL1 | ||||
| autosomal recessive spinocerebellar ataxia 21 |
| Mouse Phenotypes | muscle phenotype |
decreased myocardial fiber size |
decreased skeletal muscle fiber diameter |
increased variability of skeletal muscle fiber size |
centrally nucleated skeletal muscle fibers |
skeletal muscle fiber necrosis |
abnormal skeletal muscle fiber type ratio |
skeletal muscle atrophy |
decreased skeletal muscle mass |
dystrophic muscle |
muscular atrophy |
abnormal muscle electrophysiology |
abnormal muscle regeneration |
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| Availability | Mouse Genotype | |||||||||||||
| Scyl1mdf/Scyl1mdf | ||||||||||||||
| Scyl1tm1.1Spel/Scyl1tm1.1Spel | ||||||||||||||
| Scyl1tm1Spel/Scyl1tm1Spel Tg(Ckmm-cre)5Khn/0 (conditional) |
* | |||||||||||||
| Scyl1tm1Spel/Scyl1tm1Spel Tg(Nes-cre)1Kln/0 (conditional) |
* | |||||||||||||
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 06/12/2024 MGI 6.13 |
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