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Symbol
Name
ID

Agrn
agrin
MGI:87961

Phenotype annotations related to muscle

*	Aspects of the system are reported to show a normal phenotype.
!	Indicates phenotype varies with strain background.
	Darker colors indicate more annotations

Human Phenotypes	Weakness of facial musculature	EMG: decremental response of compound muscle action potential to repetitive nerve stimulation	Difficulty running	Easy fatigability	Proximal muscle weakness
Disease(s) Associated with AGRN
congenital myasthenic syndrome 8

Mouse Phenotypes		muscle phenotype	abnormal diaphragm morphology	abnormal skeletal muscle fiber type ratio	skeletal muscle atrophy	muscle spasm	myopathy
Availability	Mouse Genotype	muscle phenotype	abnormal diaphragm morphology	abnormal skeletal muscle fiber type ratio	skeletal muscle atrophy	muscle spasm	myopathy
	Agrn^nmf380/Agrn^nmf380	*!			!
	Agrn^tm1Rwb/Agrn^tm1Rwb Tg(Pax3-cre)1Joe/0 (conditional)

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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