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Symbol Name ID |
Sod1
superoxide dismutase 1, soluble MGI:98351 |
| Darker colors indicate more annotations |
| Human Phenotypes | Abnormal cardiovascular system morphology |
Atrial septal defect |
Patent foramen ovale |
Secundum atrial septal defect |
Ventricular septal defect |
Atrioventricular canal defect |
Complete atrioventricular canal defect |
Double outlet right ventricle |
Tetralogy of Fallot |
Ebstein anomaly of the tricuspid valve |
Pulmonary artery stenosis |
Partial anomalous pulmonary venous return |
Patent ductus arteriosus |
Abnormality of the lymphatic system |
Abnormal retinal vascular morphology |
Attenuation of retinal blood vessels |
| Disease(s) Associated with SOD1 | ||||||||||||||||
| Down syndrome | ||||||||||||||||
| retinitis pigmentosa |
| Mouse Phenotypes | myocardium necrosis |
abnormal cardiovascular system physiology |
decreased cardiac muscle contractility |
increased myocardial infarct size |
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| Availability | Mouse Genotype | ||||
| Sod1tm1Dkd/Sod1tm1Dkd | |||||
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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