Symbol Name ID |
Agrn
agrin MGI:87961 |
* | 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 |
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Availability | Mouse Genotype | ||||||
Agrnnmf380/Agrnnmf380 | *! | ! | |||||
Agrntm1Rwb/Agrntm1Rwb Tg(Pax3-cre)1Joe/0 (conditional) |
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 09/03/2024 MGI 6.24 |
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