|
Symbol Name ID |
Rapsn
receptor-associated protein of the synapse MGI:99422 |
| Darker colors indicate more annotations |
| Human Phenotypes | Flexion contracture |
Arthrogryposis multiplex congenita |
Hypotonia |
Neonatal hypotonia |
EMG: decremental response of compound muscle action potential to repetitive nerve stimulation |
Difficulty running |
Easy fatigability |
Generalized muscle weakness |
Gowers sign |
| Disease(s) Associated with RAPSN | |||||||||
| congenital myasthenic syndrome 11 | |||||||||
| fetal akinesia deformation sequence syndrome 2 |
| Mouse Phenotypes | muscle weakness |
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| Availability | Mouse Genotype | |
| Rapsntm1Jrs/Rapsntm1Jrs | ||
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 05/14/2024 MGI 6.23 |
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