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Symbol Name ID |
Magel2
MAGE family member L2 MGI:1351648 |
| Darker colors indicate more annotations |
| Human Phenotypes | Type II diabetes mellitus |
Hypothalamic luteinizing hormone-releasing hormone deficiency |
Small pituitary gland |
Central hypothyroidism |
Absence of pubertal development |
Precocious puberty |
Premature pubarche |
Hypogonadism |
| Disease(s) Associated with MAGEL2 | ||||||||
| Schaaf-Yang syndrome |
| Mouse Phenotypes | abnormal corpus luteum morphology |
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| Availability | Mouse Genotype | |
| Magel2tm1Stw/Magel2+ | ||
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 05/14/2024 MGI 6.23 |
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