F11 (coagulation factor XI)

2003-05-01  

Identity

HGNC
LOCATION
4q35.2
LOCUSID
ALIAS
FXI,PTA
FUSION GENES

Other Information

Locus ID:

NCBI: 2160
MIM: 264900
HGNC: 3529
Ensembl: ENSG00000088926

Variants:

dbSNP: 2160
ClinVar: 2160
TCGA: ENSG00000088926
COSMIC: F11

RNA/Proteins

Gene IDTranscript IDUniprot
ENSG00000088926ENST00000264691X6R3B1
ENSG00000088926ENST00000264692P03951
ENSG00000088926ENST00000403665P03951
ENSG00000088926ENST00000452239H0Y596
ENSG00000088926ENST00000492972D6RB32

Expression (GTEx)

0
10
20
30
40
50
60

Pathways

PathwaySourceExternal ID
Complement and coagulation cascadesKEGGko04610
Complement and coagulation cascadesKEGGhsa04610
HemostasisREACTOMER-HSA-109582
Formation of Fibrin Clot (Clotting Cascade)REACTOMER-HSA-140877
Intrinsic Pathway of Fibrin Clot FormationREACTOMER-HSA-140837

PharmGKB

Entity IDNameTypeEvidenceAssociationPKPDPMIDs
PA452637hormonal contraceptives for systemic useChemicalClinicalAnnotationassociatedPD28750087

References

Pubmed IDYearTitleCitations
381946792024Factor XI deficiency: phenotypic age-related considerations and clinical approach towards bleeding risk assessment.2
381946792024Factor XI deficiency: phenotypic age-related considerations and clinical approach towards bleeding risk assessment.2
367245092023Thrombogenic potential of picomolar coagulation factor XIa is mediated by thrombin wave propagation.0
369408032023Impact of genetic structural variants in factor XI deficiency: identification, accurate characterization, and inferred mechanism by long-read sequencing.1
371412572023The unknown functions of a known protein: the case of coagulation factor XI.0
372528922023A focus on dominant negative variants in a series of 170 heterozygous FXI-deficient patients.0
374609822023Elevated plasma factor XI predicts cardiovascular events in patients with type 2 diabetes: a long-term observational study.3
379061342023[Analysis of a Chinese pedigree affected with Hereditary coagulation factor Ⅺ deficiency due to variant of F11 gene].0
367245092023Thrombogenic potential of picomolar coagulation factor XIa is mediated by thrombin wave propagation.0
369408032023Impact of genetic structural variants in factor XI deficiency: identification, accurate characterization, and inferred mechanism by long-read sequencing.1
371412572023The unknown functions of a known protein: the case of coagulation factor XI.0
372528922023A focus on dominant negative variants in a series of 170 heterozygous FXI-deficient patients.0
374609822023Elevated plasma factor XI predicts cardiovascular events in patients with type 2 diabetes: a long-term observational study.3
379061342023[Analysis of a Chinese pedigree affected with Hereditary coagulation factor Ⅺ deficiency due to variant of F11 gene].0
353775292022Sulfonated non-saccharide molecules and human factor XIa: Enzyme inhibition and computational studies.5

Citation

Dessen P

F11 (coagulation factor XI)

Atlas Genet Cytogenet Oncol Haematol. 2003-05-01

Online version: http://atlasgeneticsoncology.org/gene/40519/f11