FBN1
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Fibrillin-1 is a protein that in humans is encoded by the FBN1 gene, located on chromosome 15.[4][5]
This gene encodes a member of the fibrillin family. The encoded protein is a large, extracellular matrix glycoprotein that serves as a structural component of 10-12 nm calcium-binding microfibrils. These microfibrils provide force bearing structural support in elastic and nonelastic connective tissue throughout the body. Mutations in this gene are associated with Marfan syndrome, isolated ectopia lentis, autosomal dominant Weill-Marchesani syndrome, MASS syndrome, and Shprintzen-Goldberg craniosynostosis syndrome.[6]
Clinical significance
Mutations in FBN1 and FBN2 are associated with adolescent idiopathic scoliosis .[7]
See also
References
- ↑ "Diseases that are genetically associated with FBN1 view/edit references on wikidata".
- ↑ "Human PubMed Reference:".
- ↑ "Mouse PubMed Reference:".
- ↑ Biery NJ, Eldadah ZA, Moore CS, Stetten G, Spencer F, Dietz HC (Feb 1999). "Revised genomic organization of FBN1 and significance for regulated gene expression". Genomics. 56 (1): 70–7. doi:10.1006/geno.1998.5697. PMID 10036187.
- ↑ Faivre L, Gorlin RJ, Wirtz MK, Godfrey M, Dagoneau N, Samples JR, Le Merrer M, Collod-Beroud G, Boileau C, Munnich A, Cormier-Daire V (Jan 2003). "In frame fibrillin-1 gene deletion in autosomal dominant Weill-Marchesani syndrome". Journal of Medical Genetics. 40 (1): 34–6. doi:10.1136/jmg.40.1.34. PMC 1735272
. PMID 12525539. - ↑ "Entrez Gene: FBN1 fibrillin 1".
- ↑ Buchan JG, Alvarado DM, Haller GE, Cruchaga C, Harms MB, Zhang T, Willing MC, Grange DK, Braverman AC, Miller NH, Morcuende JA, Tang NL, Lam TP, Ng BK, Cheng JC, Dobbs MB, Gurnett CA (Oct 2014). "Rare variants in FBN1 and FBN2 are associated with severe adolescent idiopathic scoliosis". Human Molecular Genetics. 23 (19): 5271–82. doi:10.1093/hmg/ddu224. PMID 24833718.
External links
Further reading
- Hayward C, Brock DJ (1998). "Fibrillin-1 mutations in Marfan syndrome and other type-1 fibrillinopathies". Human Mutation. 10 (6): 415–23. doi:10.1002/(SICI)1098-1004(1997)10:6<415::AID-HUMU1>3.0.CO;2-C. PMID 9401003.
- Robinson PN, Godfrey M (Jan 2000). "The molecular genetics of Marfan syndrome and related microfibrillopathies". Journal of Medical Genetics. 37 (1): 9–25. doi:10.1136/jmg.37.1.9. PMC 1734449. PMID 10633129.
- Handford PA (Dec 2000). "Fibrillin-1, a calcium binding protein of extracellular matrix". Biochimica et Biophysica Acta. 1498 (2-3): 84–90. doi:10.1016/s0167-4889(00)00085-9. PMID 11108952.
- Robinson PN, Booms P, Katzke S, Ladewig M, Neumann L, Palz M, Pregla R, Tiecke F, Rosenberg T (Sep 2002). "Mutations of FBN1 and genotype-phenotype correlations in Marfan syndrome and related fibrillinopathies". Human Mutation. 20 (3): 153–61. doi:10.1002/humu.10113. PMID 12203987.
- Adès LC, Holman KJ, Brett MS, Edwards MJ, Bennetts B (Apr 2004). "Ectopia lentis phenotypes and the FBN1 gene". American Journal of Medical Genetics Part A. 126A (3): 284–9. doi:10.1002/ajmg.a.20605. PMID 15054843.
- Milewicz DM, Dietz HC, Miller DC (Mar 2005). "Treatment of aortic disease in patients with Marfan syndrome". Circulation. 111 (11): e150–7. doi:10.1161/01.CIR.0000155243.70456.F4. PMID 15781745.
- Boileau C, Jondeau G, Mizuguchi T, Matsumoto N (May 2005). "Molecular genetics of Marfan syndrome". Current Opinion in Cardiology. 20 (3): 194–200. doi:10.1097/01.hco.0000162398.21972.cd. PMID 15861007.
- Whiteman P, Hutchinson S, Handford PA (2006). "Fibrillin-1 misfolding and disease". Antioxidants & Redox Signaling. 8 (3-4): 338–46. doi:10.1089/ars.2006.8.338. PMID 16677079.
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