Symbol
Name
ID

Magel2
MAGE family member L2
MGI:1351648

Phenotype annotations related to behavior/neurological

Darker colors indicate more annotations

Human Phenotypes

Decreased fetal movement

Fetal akinesia sequence

Feeding difficulties

Poor suck

Nasogastric tube feeding

Atypical behavior

Lethargy

Autistic behavior

Polyphagia

Abnormal temper tantrums

Compulsive behaviors

Impulsivity

Skin-picking

Weak cry

Disease(s) Associated with MAGEL2

Schaaf-Yang syndrome

Mouse Phenotypes		decreased compensatory feeding amount	absent gastric milk in neonates	abnormal suckling behavior	decreased grip strength	abnormal locomotor behavior	abnormal locomotor circadian rhythm	decreased vertical activity	decreased locomotor activity	abnormal circadian behavior	pup cannibalization
Availability	Mouse Genotype	decreased compensatory feeding amount	absent gastric milk in neonates	abnormal suckling behavior	decreased grip strength	abnormal locomotor behavior	abnormal locomotor circadian rhythm	decreased vertical activity	decreased locomotor activity	abnormal circadian behavior	pup cannibalization
	Magel2^em2(IMPC)H/Magel2^em2(IMPC)H
	Magel2^tm1Stw/Magel2^tm1Stw
	Magel2^tm1.1Mus/Magel2⁺
	Magel2^tm1Stw/Magel2⁺

Contributing Projects: 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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