Symbol Name ID |
Mypn
myopalladin MGI:1916052 |
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 |
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Availability | Mouse Genotype | |||||
Mypntm1.1Epu/Mypntm1.1Epu | ||||||
Mypntm1.1Epu/Mypn+ |
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 04/09/2024 MGI 6.23 |
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