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Symbol Name ID |
Bin1
bridging integrator 1 MGI:108092 |
| Darker colors indicate more annotations |
| Human Phenotypes | Facial palsy |
Scapular winging |
Flexion contracture |
Neonatal hypotonia |
EMG: myopathic abnormalities |
Axial muscle weakness |
Distal muscle weakness |
Proximal muscle weakness |
Gowers sign |
Respiratory insufficiency due to muscle weakness |
Centrally nucleated skeletal muscle fibers |
Generalized amyotrophy |
| Disease(s) Associated with BIN1 | ||||||||||||
| centronuclear myopathy 2 |
| Mouse Phenotypes | abnormal myocardial fiber morphology |
disorganized myocardium |
ventricular cardiomyopathy |
abnormal sarcomere morphology |
abnormal A band morphology |
diffuse Z line |
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| Availability | Mouse Genotype | ||||||
| Bin1tm1Gcp/Bin1tm1Gcp | |||||||
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 04/23/2024 MGI 6.23 |
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