Homo sapiens fibrillin 1 (FBN1), RefSeqGene (LRG_778) on chromosome 15

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[Correlation of posterior segment lesions with anterior segment biometric parameters and FBN1 genotype in patients with Marfan syndrome]. [Zhonghua Yan Ke Za Zhi. 2024]
[Correlation of posterior segment lesions with anterior segment biometric parameters and FBN1 genotype in patients with Marfan syndrome].
Liu Y, Chen TH, Jiang YX. Zhonghua Yan Ke Za Zhi. 2024 Jul 11; 60(7):601-610.
Causative role of a novel intronic indel variant in FBN1 and maternal germinal mosaicism in Marfan syndrome. [Orphanet J Rare Dis. 2024]
Causative role of a novel intronic indel variant in FBN1 and maternal germinal mosaicism in Marfan syndrome.
Bai Y, Sun Y, Yu C, Xia Y, Wu J, Wang L, Gao Y, Tu X, Kong X. Orphanet J Rare Dis. 2024 May 21; 19(1):209. Epub 2024 May 21.
Targeted genetic analysis in a cohort of sporadic death from spontaneous rupture of thoracic aortic dissection in Han Chinese population. [Forensic Sci Int Genet. 2024]
Targeted genetic analysis in a cohort of sporadic death from spontaneous rupture of thoracic aortic dissection in Han Chinese population.
Zhao Q, Zhou N, Wu Q, Zhang K, Yue J, Zheng D, Wang Y, Xiao Y, Li R, Cheng R, et al. Forensic Sci Int Genet. 2024 Jul; 71:103051. Epub 2024 Apr 22.

RefSeq alternative splicing
See 4 reference mRNA sequence splice variants for the FBN1 gene.

Protein
Protein sequence from Nucleotide coding region
PubMed
PubMed articles cited by Nucleotide sequence record
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OMIM records associated with Nucleotide sequence
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RNA
RNA sequence records that are annotated on the current genomic nucleotide sequences. The RNA records represent aligned or predicted transcripts of the current records.
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Nucleotide