F8

GENERAL INFORMATION

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Gene name

F8

Gene description

Coagulation factor VIII, procoagulant component

Protein class

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

Predicted localization

Intracellular,Secreted

Number of transcripts

4
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HUMAN PROTEIN ATLAS INFORMATION

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RNA tissue category

HPA:Expressed in all
GTEx:Expressed in all

Protein evidence

Evidence at protein level

Protein localization

Extracellular deposits and cytoplasmic expression in most tissues.

ANTIBODY RELIABILITY

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Data reliability
description

Antibody staining mainly consistent with RNA expression data. Secreted protein, tissue location of RNA and protein might differ and correlation is complex.

Data reliability

Supportive based on 1 antibody.
CAB018777
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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
Liver & gallbladder
Pancreas
Gastrointestinal tract
Kidney & urinary bladder
Male tissues
Female tissues
Adipose & soft tissue
Skin
Cerebral cortex

Lymph node

Liver

Colon

Kidney

Testis



PROTEIN EXPRESSION OVERVIEW

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Organ

Expression



RNA EXPRESSION OVERVIEW

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HPA dataset
RNA tissue category:  Expressed in all

Organ

Expression

GTEx dataset
RNA tissue category:  Expressed in all

Organ

Expression



GENE INFORMATION

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Gene name

F8 (HGNC Symbol)

Synonyms

DXS1253E, F8C, FVIII, HEMA

Description

Coagulation factor VIII, procoagulant component (HGNC Symbol)

Entrez gene summary

This gene encodes coagulation factor VIII, which participates in the intrinsic pathway of blood coagulation; factor VIII is a cofactor for factor IXa which, in the presence of Ca+2 and phospholipids, converts factor X to the activated form Xa. This gene produces two alternatively spliced transcripts. Transcript variant 1 encodes a large glycoprotein, isoform a, which circulates in plasma and associates with von Willebrand factor in a noncovalent complex. This protein undergoes multiple cleavage events. Transcript variant 2 encodes a putative small protein, isoform b, which consists primarily of the phospholipid binding domain of factor VIIIc. This binding domain is essential for coagulant activity. Defects in this gene results in hemophilia A, a common recessive X-linked coagulation disorder. [provided by RefSeq, Jul 2008]

Chromosome

X

Cytoband

q28

Chromosome location (bp)

154835788 - 155026940

Protein evidence

Evidence at protein level (all genes)

Ensembl

ENSG00000185010 (version 78.38)

Entrez gene

2157

UniProt

P00451 (UniProt - Evidence at protein level)

neXtProt

NX_P00451

Antibodypedia

F8 antibodies


PROTEIN BROWSER

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ENST00000330287
 
ENST00000360256
 
ENST00000423959
 
ENST00000453950
 
 
 
 


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)

F8-001 ENSP00000353393
ENST00000360256
P00451
Show all »
Show » Show » 2351 267 Yes 0
F8-003 ENSP00000327895
ENST00000330287
P00451
Show all »
Show » Show » 216 24.6 No 0
F8-004 ENSP00000409446
ENST00000423959
B1B0G8
Show all »
Show » Show » 222 25 No 0
F8-005 ENSP00000389153
ENST00000453950
B1B0G9
Show all »
Show » Show » 165 18.7 No 0