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Symbol Name ID |
Magel2
MAGE family member L2 MGI:1351648 |
| Darker colors indicate more annotations |
| Human Phenotypes | Frontal bossing |
Mandibular prognathia |
Retrognathia |
Tapered finger |
Clinodactyly |
Brachydactyly |
Rocker bottom foot |
Short foot |
Small hand |
Flexion contracture |
Arthrogryposis multiplex congenita |
Camptodactyly |
Hip dysplasia |
Kyphosis |
Scoliosis |
Osteopenia |
Osteoporosis |
| Disease(s) Associated with MAGEL2 | |||||||||||||||||
| Schaaf-Yang syndrome |
| Mouse Phenotypes | scoliosis |
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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 04/16/2024 MGI 6.23 |
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