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Homo sapiens coagulation factor VII (F7), RefSeqGene (LRG_554) on chromosome 13

NCBI Reference Sequence: NG_009262.1

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Articles about the F7 gene

[Pedigree Analysis of Hereditary Coagulation Factor XII Deficiency Caused by Compound Heterozygous Mutation p.Gly175Cys and p.Gly542Ser of F12 Gene]. [Zhongguo Shi Yan Xue Ye Xue Za...]
[Pedigree Analysis of Hereditary Coagulation Factor XII Deficiency Caused by Compound Heterozygous Mutation p.Gly175Cys and p.Gly542Ser of F12 Gene].
Cheng XL, Yang T, Yang L, Xin YJ, He M, Zhu L, Liu JY. Zhongguo Shi Yan Xue Ye Xue Za Zhi. 2024 Jun; 32(3):862-867.
[Congenital FⅦ Deficiency Associated with a Novel Mutation in F7 Gene]. [Zhongguo Shi Yan Xue Ye Xue Za...]
[Congenital FⅦ Deficiency Associated with a Novel Mutation in F7 Gene].
Wang YY, Zhang YG, Chen WB. Zhongguo Shi Yan Xue Ye Xue Za Zhi. 2024 Jun; 32(3):857-861.
Frequency of the p.Thr241Asn mutation in Chinese patients with congenital factor VII deficiency. [Thromb Res. 2024]
Frequency of the p.Thr241Asn mutation in Chinese patients with congenital factor VII deficiency.
Zhou P, Peng Y, Li Q, Huang Q, Kong Y. Thromb Res. 2024 Mar; 235:122-124. Epub 2024 Feb 6.

Reference sequence information

RefSeq alternative splicing
See 13 reference mRNA sequence splice variants for the F7 gene.

More about the F7 gene

This gene encodes coagulation factor VII which is a vitamin K-dependent factor essential for hemostasis. This factor circulates in the blood...
Also Known As: SPCA

Related information

Protein
Protein sequence from Nucleotide coding region
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