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 |
|
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 08/02/2024 MGI 6.24 |
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