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Symbol Name ID |
Dnm1l
dynamin 1-like MGI:1921256 |
| Darker colors indicate more annotations |
| Human Phenotypes | Neonatal respiratory distress |
| Disease(s) Associated with DNM1L | |
| encephalopathy due to defective mitochondrial and peroxisomal fission 1 |
| Mouse Phenotypes | pulmonary vascular congestion |
pleural effusion |
tachypnea |
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| Availability | Mouse Genotype | |||
| Dnm1lPy/Dnm1l+ | ||||
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 04/30/2024 MGI 6.23 |
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