|
Symbol Name ID |
Magel2
MAGE family member L2 MGI:1351648 |
| * | Aspects of the system are reported to show a normal phenotype. |
| Darker colors indicate more annotations |
| Human Phenotypes | Hypothalamic luteinizing hormone-releasing hormone deficiency |
Small pituitary gland |
Ventriculomegaly |
Absent speech |
Delayed speech and language development |
Psychosis |
Atypical behavior |
Lethargy |
Autistic behavior |
Polyphagia |
Abnormal temper tantrums |
Compulsive behaviors |
Impulsivity |
Skin-picking |
Cognitive impairment |
Intellectual disability |
Intellectual disability, borderline |
Intellectual disability, mild |
Abnormal rapid eye movement sleep |
Confusional arousal |
Sleep apnea |
Central sleep apnea |
Obstructive sleep apnea |
Reduced tendon reflexes |
Inability to walk |
Brain imaging abnormality |
Neurodevelopmental delay |
Global developmental delay |
Motor delay |
Delayed ability to walk |
Specific learning disability |
Seizure |
Impaired temperature sensation |
| Disease(s) Associated with MAGEL2 | |||||||||||||||||||||||||||||||||
| Schaaf-Yang syndrome |
| Mouse Phenotypes | nervous system phenotype |
abnormal hypothalamus secretion |
|
| Availability | Mouse Genotype | ||
| Magel2tm1.1Mus/Magel2+ | * | ||
Mouse Genome Database (MGD), Gene Expression Database (GXD), Mouse Models of Human Cancer database (MMHCdb) (formerly Mouse Tumor Biology (MTB)), Gene Ontology (GO) |
||
|
Citing These Resources Funding Information Warranty Disclaimer, Privacy Notice, Licensing, & Copyright Send questions and comments to User Support. |
last database update 05/14/2024 MGI 6.23 |
|
|
|
||
Analysis Tools