Homo sapiens Gene: F11 | |||||||||||||||||||
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Summary | |||||||||||||||||||
InnateDB Gene | IDBG-47627.6 | ||||||||||||||||||
Last Modified | 2014-10-13 [Report errors or provide feedback] | ||||||||||||||||||
Gene Symbol | F11 | ||||||||||||||||||
Gene Name | coagulation factor XI | ||||||||||||||||||
Synonyms | FXI | ||||||||||||||||||
Species | Homo sapiens | ||||||||||||||||||
Ensembl Gene | ENSG00000088926 | ||||||||||||||||||
Encoded Proteins |
coagulation factor XI
coagulation factor XI
coagulation factor XI
coagulation factor XI
coagulation factor XI
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Protein Structure | |||||||||||||||||||
Useful resources | Stemformatics EHFPI ImmGen | ||||||||||||||||||
InnateDB Annotation | |||||||||||||||||||
Summary |
F11 modulates the inflammatory response of PMN leukocytes by reducing chemotaxis triggered by IL8 or fMLP, highlighting the interplay between inflammation and coagulation (Demonstrated in mouse)
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InnateDB Annotation from Orthologs | |||||||||||||||||||
Summary |
[Mus musculus] F11 modulates the inflammatory response of PMN leukocytes by reducing chemotaxis triggered by Il8 or fMLP, highlighting the interplay between inflammation and coagulation.
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Entrez Gene | |||||||||||||||||||
Summary |
This gene encodes coagulation factor XI of the blood coagulation cascade. This protein is present in plasma as a zymogen, which is a unique plasma coagulation enzyme because it exists as a homodimer consisting of two identical polypeptide chains linked by disulfide bonds. During activation of the plasma factor XI, an internal peptide bond is cleaved by factor XIIa (or XII) in each of the two chains, resulting in activated factor XIa, a serine protease composed of two heavy and two light chains held together by disulfide bonds. This activated plasma factor XI triggers the middle phase of the intrisic pathway of blood coagulation by activating factor IX. Defects in this factor lead to Rosenthal syndrome, a blood coagulation abnormality. [provided by RefSeq, Jul 2008] |
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Gene Information | |||||||||||||||||||
Type | Protein coding | ||||||||||||||||||
Genomic Location | Chromosome 4:186265945-186288806 | ||||||||||||||||||
Strand | Forward strand | ||||||||||||||||||
Band | q35.2 | ||||||||||||||||||
Transcripts |
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Interactions | |||||||||||||||||||
Number of Interactions |
This gene and/or its encoded proteins are associated with 8 experimentally validated interaction(s) in this database.
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Gene Ontology | |||||||||||||||||||
Molecular Function |
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Biological Process |
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Cellular Component |
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Orthologs | |||||||||||||||||||
Species
Mus musculus
Bos taurus
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Gene ID
Gene Order
Not yet available
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Pathways | |||||||||||||||||||
NETPATH | |||||||||||||||||||
REACTOME |
Intrinsic Pathway pathway
Formation of Fibrin Clot (Clotting Cascade) pathway
Hemostasis pathway
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KEGG |
Complement and coagulation cascades pathway
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INOH | |||||||||||||||||||
PID NCI | |||||||||||||||||||
Cross-References | |||||||||||||||||||
SwissProt | |||||||||||||||||||
TrEMBL | Q9UEG0 | ||||||||||||||||||
UniProt Splice Variant | |||||||||||||||||||
Entrez Gene | 2160 | ||||||||||||||||||
UniGene | |||||||||||||||||||
RefSeq | NM_000128 XM_005262821 XM_005262824 XM_005262825 | ||||||||||||||||||
HUGO | HGNC:3529 | ||||||||||||||||||
OMIM | 264900 | ||||||||||||||||||
CCDS | CCDS3847 | ||||||||||||||||||
HPRD | 07524 | ||||||||||||||||||
IMGT | |||||||||||||||||||
EMBL | AB004057 | ||||||||||||||||||
GenPept | BAA20295 | ||||||||||||||||||
RNA Seq Atlas | 2160 | ||||||||||||||||||