F5

GENERAL INFORMATION

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Gene name

F5

Gene description

Coagulation factor V (proaccelerin, labile factor)

Protein class

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

Predicted localization

Secreted

Number of transcripts

2
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HUMAN PROTEIN ATLAS INFORMATION

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RNA tissue category

HPA:Group enriched (gallbladder, liver, placenta)
GTEx:Tissue enriched (liver)

Protein evidence

Evidence at protein level

Protein localization

Cytoplasmic expression and extracellular positivity in several different tissue types.

ANTIBODY RELIABILITY

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Data reliability
description

Secreted protein, tissue location of RNA and protein might differ and correlation is complex. Antibody staining in cells/structures not annotated, view images.

Data reliability

Uncertain based on 1 antibody.
HPA002036
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RNA AND PROTEIN EXPRESSION SUMMARY

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RNA expression (FPKM) Protein expression (score)
Brain
Endocrine tissues
Bone marrow & immune system
Muscle tissues
Lung
Bronchus
N/A
N/A
Liver & gallbladder
Pancreas
Gastrointestinal tract
Kidney & urinary bladder
Male tissues
Female tissues
Adipose & soft tissue
Skin
Cerebral cortex

Lymph node

Liver

Colon

Kidney

Testis

Placenta



PROTEIN EXPRESSION OVERVIEW

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Organ

Expression



RNA EXPRESSION OVERVIEW

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HPA dataset
RNA tissue category:  Group enriched (gallbladder, liver, placenta)

Organ

Expression

GTEx dataset
RNA tissue category:  Tissue enriched (liver)

Organ

Expression



GENE INFORMATION

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Gene name

F5

Synonyms

Description

Coagulation factor V (proaccelerin, labile factor) (HGNC Symbol)

Entrez gene summary

This gene encodes an essential cofactor of the blood coagulation cascade. This factor circulates in plasma, and is converted to the active form by the release of the activation peptide by thrombin during coagulation. This generates a heavy chain and a light chain which are held together by calcium ions. The activated protein is a cofactor that participates with activated coagulation factor X to activate prothrombin to thrombin. Defects in this gene result in either an autosomal recessive hemorrhagic diathesis or an autosomal dominant form of thrombophilia, which is known as activated protein C resistance. [provided by RefSeq, Oct 2008]

Chromosome

1

Cytoband

q24.2

Chromosome location (bp)

169514166 - 169586588

Protein evidence

Evidence at protein level (all genes)

Ensembl

ENSG00000198734 (version 78.38)

Entrez gene

2153

UniProt

P12259 (UniProt - Evidence at protein level)

neXtProt

NX_P12259

Antibodypedia

F5 antibodies


PROTEIN BROWSER

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ENST00000367796
 
ENST00000367797
 
 
 
 


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)

F5-001 ENSP00000356771
ENST00000367797
P12259
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Show » Show » 2224 251.7 Yes 0
F5-002 ENSP00000356770
ENST00000367796
Q2HZZ1
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Show » Show » 2229 252.2 Yes 0