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Symbol Name ID |
Magel2
MAGE family member L2 MGI:1351648 |
| Darker colors indicate more annotations |
| Human Phenotypes | Flexion contracture |
Arthrogryposis multiplex congenita |
Camptodactyly |
Infantile muscular hypotonia |
Neonatal hypotonia |
| Disease(s) Associated with MAGEL2 | |||||
| Schaaf-Yang syndrome |
| Mouse Phenotypes | decreased skeletal muscle fiber size |
increased skeletal muscle fiber size |
decreased skeletal muscle weight |
skeletal muscle atrophy |
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| Availability | Mouse Genotype | ||||
| Magel2tm1Stw/Magel2tm1Stw | |||||
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 04/30/2024 MGI 6.23 |
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