Homo sapiens fibrinogen gamma chain (FGG), transcript variant gamma, m - Nucleotide

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A novel mutation in the FGG gene causes hypofibrinogenemia in a Chinese family. [Hereditas. 2024]
A novel mutation in the FGG gene causes hypofibrinogenemia in a Chinese family.
Xie X, Du J, Geng S, Yi B, Li Q, Zuo J. Hereditas. 2024 Feb 20; 161(1):9. Epub 2024 Feb 20.
A novel missense mutation (FGG c.1168G > T) in the gamma chain of fibrinogen causing congenital hypodysfibrinogenemia with bleeding phenotype. [Hereditas. 2024]
A novel missense mutation (FGG c.1168G > T) in the gamma chain of fibrinogen causing congenital hypodysfibrinogenemia with bleeding phenotype.
Xu N, Zheng L, Dai Z, Zhu J, Xie P, Yang S, Chen F. Hereditas. 2024 Jan 18; 161(1):4. Epub 2024 Jan 18.
TRIM28-mediated nucleocapsid protein SUMOylation enhances SARS-CoV-2 virulence. [Nat Commun. 2024]
TRIM28-mediated nucleocapsid protein SUMOylation enhances SARS-CoV-2 virulence.
Ren J, Wang S, Zong Z, Pan T, Liu S, Mao W, Huang H, Yan X, Yang B, He X, et al. Nat Commun. 2024 Jan 4; 15(1):244. Epub 2024 Jan 4.

RefSeq alternative splicing
See the other reference mRNA sequence splice variant for the FGG gene (NM_021870.3).
RefSeq protein product
See the reference protein sequence for fibrinogen gamma chain isoform gamma-A precursor (NP_000500.2).

Protein
Protein sequence from Nucleotide coding region
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Nucleotide