Homo sapiens fibrinogen gamma chain (FGG), transcript variant gamma-B, - 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_000509.6).
RefSeq protein product
See the reference protein sequence for fibrinogen gamma chain isoform gamma-B precursor (NP_068656.2).

Protein
Protein sequence from Nucleotide coding region
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Mus musculus strain C57BL/6J chromosome 16, GRCm39
Mus musculus strain C57BL/6J chromosome 16, GRCm39
gi|1877089953|gnl|ASM:GCF_000000055 ef|NC_000082.7||gpp|GPC_000007828.1||gnl|NCBI_GENOMES|84

Nucleotide
Nucleotide Links for Protein (Select 270132935) (3)
Nucleotide
gem-associated protein 2 [Mus musculus]
gem-associated protein 2 [Mus musculus]
gi|153792166|ref|NP_079932.2|

Protein
Rattus norvegicus cDNA clone IMAGE:7311366
Rattus norvegicus cDNA clone IMAGE:7311366
gi|60688526|gb|BC091308.1|

Nucleotide
Homologene neighbors for GEO Profiles (Select 94721295) (0)
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Nucleotide