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Symbol Name ID |
Fbn2
fibrillin 2 MGI:95490 |
| Darker colors indicate more annotations |
| Human Phenotypes | Motor delay |
| Disease(s) Associated with FBN2 | |
| congenital contractural arachnodactyly |
| Mouse Phenotypes | abnormal brain morphology |
abnormal optic disk morphology |
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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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