| Gene Symbol | FBN2 |
| Entrez Gene ID | 2201 |
| Full Name | fibrillin 2 |
| Synonyms | CCA,DA9,EOMD |
| General protein information |
|
| Gene Type | protein-coding |
| Organism | Homo sapiens(human) |
| Genome | |
| Summary | The protein encoded by this gene is a component of connective tissue microfibrils and may be involved in elastic fiber assembly. Mutations in this gene cause congenital contractural arachnodactyly. [provided by RefSeq, Jul 2008]. |
| Disorder MIM: | |
| Disorder Html: | Contractural arachnodactyly, congenital, 121050 (3); Macular degeneration, early-onset, 616118 (3) |







































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