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Symbol Name ID |
Fbn2
fibrillin 2 MGI:95490 |
| Darker colors indicate more annotations |
| Human Phenotypes | Abnormal cardiovascular system morphology |
Atrial septal defect |
Ventricular septal defect |
Bicuspid aortic valve |
Mitral valve prolapse |
Aortic aneurysm |
Aortic root aneurysm |
Patent ductus arteriosus |
Mitral regurgitation |
| Disease(s) Associated with FBN2 | |||||||||
| congenital contractural arachnodactyly |
| Mouse Phenotypes | abnormal retina blood vessel morphology |
abnormal heart morphology |
abnormal heart weight |
enlarged heart |
prolonged ST segment |
corneal vascularization |
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| Availability | Mouse Genotype | ||||||
| Fbn2em1(IMPC)Rbrc/Fbn2em1(IMPC)Rbrc | |||||||
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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