Gene: F10-AS1
Alternate names for this Gene:
Gene Summary:
Gene is located in Chromosome:
Location in Chromosome :
Description of this Gene:
Type of Gene:
Gene: F10
Alternate names for this Gene: FX|FXA
Gene Summary: This gene encodes the vitamin K-dependent coagulation factor X of the blood coagulation cascade. This factor undergoes multiple processing steps before its preproprotein is converted to a mature two-chain form by the excision of the tripeptide RKR. Two chains of the factor are held together by 1 or more disulfide bonds; the light chain contains 2 EGF-like domains, while the heavy chain contains the catalytic domain which is structurally homologous to those of the other hemostatic serine proteases. The mature factor is activated by the cleavage of the activation peptide by factor IXa (in the intrisic pathway), or by factor VIIa (in the extrinsic pathway). The activated factor then converts prothrombin to thrombin in the presence of factor Va, Ca+2, and phospholipid during blood clotting. Mutations of this gene result in factor X deficiency, a hemorrhagic condition of variable severity. Alternative splicing results in multiple transcript variants encoding different isoforms that may undergo similar proteolytic processing to generate mature polypeptides.
Gene is located in Chromosome: 13
Location in Chromosome : 13q34
Description of this Gene: coagulation factor X
Type of Gene: protein-coding
rs121964943 in
F10-AS1;F10 gene and
Factor X Deficiency
PMID 1973167 1990 "Molecular defect (Gla+14----Lys) and its functional consequences in a hereditary factor X deficiency (factor X ""Vorarlberg"")."
PMID 12574802 2003 Impaired prothrombinase activity of factor X Gly381Asp results in severe familial CRM+ FX deficiency.
PMID 12945883 2003 A novel type I factor X variant (factor X Cys350Phe) due to loss of a disulfide bond in the catalytic domain.
PMID 19135706 2009 Characterization of a homozygous Gly11Val mutation in the Gla domain of coagulation factor X.
PMID 11248282 2001 A dysfunctional factor X (factor X San Giovanni Rotondo) present at homozygous and double heterozygous level: identification of a novel microdeletion (delC556) and missense mutation (Lys(408)-->Asn) in the factor X gene. A study of an Italian family.
PMID 15650540 2005 Genetic analysis of hereditary factor X deficiency in a French patient of Sri Lankan ancestry: in vitro expression study identified Gly366Ser substitution as the molecular basis of the dysfunctional factor X.
PMID 15075089 2004 Molecular characterization of factor X deficiency associated with borderline plasma factor X level.
PMID 10746568 2000 Molecular analysis of the genotype-phenotype relationship in factor X deficiency.
PMID 10468877 1999 A family with hereditary factor X deficiency with a point mutation Gla32 to Gln in the Gla domain (factor X Tokyo).
PMID 11728527 2001 A new factor X defect (factor X Padua 3): a compound heterozygous between true deficiency (Gly(380)-->Arg) and an abnormality (Ser(334)-->Pro).
PMID 10739379 2000 The impact of Glu102Lys on the factor X function in a patient with a doubly homozygous factor X deficiency (Gla14Lys and Glu102Lys).
PMID 8529633 1995 Functional consequences of the Ser334-->Pro mutation in a human factor X variant (factor XMarseille).
PMID 25313940 2014 Molecular dynamics characterization of five pathogenic Factor X mutants associated with decreased catalytic activity.
PMID 8910490 1996 Factor XSt. Louis II. Identification of a glycine substitution at residue 7 and characterization of the recombinant protein.
PMID 7669671 1995 Molecular bases of CRM+ factor X deficiency: a frequent mutation (Ser334Pro) in the catalytic domain and a substitution (Glu102Lys) in the second EGF-like domain.
PMID 7860069 1995 Factor XKetchikan: a variant molecule in which Gly replaces a Gla residue at position 14 in the light chain.
PMID 17393015 2007 Analysis of the novel factor X gene mutation Glu51Lys in two families with factor X-Riyadh anomaly.
PMID 26222694 2015 Frequency of the p.Gly262Asp mutation in congenital Factor X deficiency.
PMID 2790181 1989 Molecular characterization of human factor XSan Antonio.
PMID 8845463 1996 Factor X Stockton: a mild bleeding diathesis associated with an active site mutation in factor X.
rs776906 in
F10-AS1;F10 gene and
von Willebrand's factor (lab test)
PMID 23381943 2013 Ischemic stroke is associated with the ABO locus: the EuroCLOT study.