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Symbol
Name
ID

Mypn
myopalladin
MGI:1916052

Phenotype annotations related to muscle

Darker colors indicate more annotations

Human Phenotypes	Facial palsy	Scapular winging	Muscle weakness	Gowers sign	Type 1 muscle fiber predominance	Nemaline bodies
Disease(s) Associated with MYPN
nemaline myopathy 11

Mouse Phenotypes		abnormal myocardial fiber morphology	abnormal intercalated disk morphology	abnormal cardiac muscle relaxation	abnormal Z line morphology	myopathy
Availability	Mouse Genotype	abnormal myocardial fiber morphology	abnormal intercalated disk morphology	abnormal cardiac muscle relaxation	abnormal Z line morphology	myopathy
	Mypn^tm1.1Epu/Mypn^tm1.1Epu
	Mypn^tm1.1Epu/Mypn⁺

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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