F11

GENERAL INFORMATION

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Gene name

F11

Gene description

Coagulation factor XI

Protein class

Candidate cardiovascular disease genes
Disease related genes
Enzymes
FDA approved drug targets
Plasma proteins
Predicted intracellular proteins
Predicted secreted proteins

Predicted localization

Intracellular,Secreted

Number of transcripts

5
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HUMAN PROTEIN ATLAS INFORMATION

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RNA tissue category

HPA:Tissue enhanced (liver)
GTEx:Tissue enriched (liver)

Protein evidence

Evidence at protein level

ANTIBODY RELIABILITY

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Data reliability

Pending normal tissue annotation.
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RNA AND PROTEIN EXPRESSION SUMMARY

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RNA expression (FPKM) Protein expression (score)
Brain
N/A
Endocrine tissues
N/A
Bone marrow & immune system
N/A
Muscle tissues
N/A
Lung
N/A
Nasopharynx
N/A
N/A
Bronchus
N/A
N/A
Lung
N/A
Liver & gallbladder
N/A
Liver
N/A
Pancreas
N/A
Pancreas
N/A
Gastrointestinal tract
N/A
Kidney & urinary bladder
N/A
Male tissues
N/A
Testis
N/A
Epididymis
N/A
N/A
Prostate
N/A
Seminal vesicle
N/A
N/A
Female tissues
N/A
Breast
N/A
N/A
Vagina
N/A
N/A
Cervix, uterine
N/A
N/A
Ovary
N/A
Placenta
N/A
Adipose & soft tissue
N/A
Skin
N/A
Skin
N/A


PROTEIN EXPRESSION OVERVIEW

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Pending normal tissue annotation.


RNA EXPRESSION OVERVIEW

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HPA dataset
RNA tissue category:  Tissue enhanced (liver)

Organ

Expression

GTEx dataset
RNA tissue category:  Tissue enriched (liver)

Organ

Expression



GENE INFORMATION

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Gene name

F11 (HGNC Symbol)

Synonyms

FXI

Description

Coagulation factor XI (HGNC Symbol)

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]

Chromosome

4

Cytoband

q35.2

Chromosome location (bp)

186265945 - 186288806

Protein evidence

Evidence at protein level (all genes)

Ensembl

ENSG00000088926 (version 78.38)

Entrez gene

2160

UniProt

P03951 (UniProt - Evidence at protein level)

neXtProt

NX_P03951

Antibodypedia

F11 antibodies


PROTEIN BROWSER

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ENST00000264691
 
ENST00000264692
 
ENST00000403665
 
ENST00000452239
 
ENST00000492972
 
 
 
 


PROTEIN INFORMATION

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Splice variant

Ensembl

UniProt

Protein class

Gene ontology

Length
(aa)

Molecular mass
(kDa)

Signal peptide
(predicted)

Transmembrane regions
(predicted)

F11-001 ENSP00000384957
ENST00000403665
P03951
Show all »
Show » Show » 625 70.1 Yes 0
F11-002 ENSP00000424479
ENST00000492972
D6RB32
Show all »
Show » Show » 162 18.5 Yes 0
F11-003 ENSP00000397401
ENST00000452239
Q9UEG0
Show all »
Show » Show » 210 23 No 0
F11-007 ENSP00000264691
ENST00000264691
Show » Show » 159 17.9 No 0
F11-201 ENSP00000264692
ENST00000264692
P03951
Show all »
Show » Show » 571 63.8 Yes 0