Homo sapiens fibrillin 1 (FBN1), transcript variant 1, mRNA

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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 protein product
See the reference protein sequence for fibrillin-1 isoform a preproprotein (NP_000129.3).

Protein
Protein sequence from Nucleotide coding region
PubMed
PubMed articles cited by Nucleotide sequence record
Taxonomy
Taxonomy sequences associated with Nucleotide record
Annotated Genomic
Genomic sequence records that have the current RNA records as annotated features marking the exons of genes.
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BioSystems
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Components (Core)
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OMIM
OMIM records associated with Nucleotide sequence
Probe
Related Probe entry
PubMed (RefSeq)
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PubMed (Weighted)
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