Homo sapiens mRNA for KIAA1776 protein (fibrillin3)

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Genetic Insights into Skeletal Malocclusion: The Role of the FBN3 rs7351083 SNP in the Romanian Population. [Medicina (Kaunas). 2024]
Genetic Insights into Skeletal Malocclusion: The Role of the FBN3 rs7351083 SNP in the Romanian Population.
Topârcean AM, Acatrinei A, Rusu I, Feștilă D, Câmpian RS, Kelemen B, Ghergie MCD. Medicina (Kaunas). 2024 Jun 27; 60(7). Epub 2024 Jun 27.
Engagement of the G3BP2-TRIM25 Interaction by Nucleocapsid Protein Suppresses the Type I Interferon Response in SARS-CoV-2-Infected Cells. [Vaccines (Basel). 2022]
Engagement of the G3BP2-TRIM25 Interaction by Nucleocapsid Protein Suppresses the Type I Interferon Response in SARS-CoV-2-Infected Cells.
Yang Z, Li J, Li J, Zheng H, Li H, Lai Q, Chen Y, Qin L, Zuo Y, Guo L, et al. Vaccines (Basel). 2022 Nov 29; 10(12). Epub 2022 Nov 29.
Further delineation of familial polycystic ovary syndrome (PCOS) via whole-exome sequencing: PCOS-related rare FBN3 and FN1 gene variants are identified. [J Obstet Gynaecol Res. 2022]
Further delineation of familial polycystic ovary syndrome (PCOS) via whole-exome sequencing: PCOS-related rare FBN3 and FN1 gene variants are identified.
Karakaya C, Çil AP, Bilguvar K, Çakir T, Karalok MH, Karabacak RO, Caglayan AO. J Obstet Gynaecol Res. 2022 May; 48(5):1202-1211. Epub 2022 Feb 9.

RefSeq alternative splicing
See 18 reference mRNA sequence splice variants for the FBN3 gene.

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Nucleotide