FGA

GENERAL INFORMATION

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Gene name

FGA

Gene description

Fibrinogen alpha chain

Protein class

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

Predicted localization

Secreted

Number of transcripts

3
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HUMAN PROTEIN ATLAS INFORMATION

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RNA tissue category

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

Protein evidence

Evidence at protein level

Protein localization

Distinct plasma positivity.

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

Supportive based on 3 antibodies.
HPA051370 , HPA064755 , CAB016776
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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

Small intestine

Colon

Kidney

Testis



PROTEIN EXPRESSION OVERVIEW

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Organ

Expression



RNA EXPRESSION OVERVIEW

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HPA dataset
RNA tissue category:  Tissue enriched (liver)

Organ

Expression

GTEx dataset
RNA tissue category:  Tissue enriched (liver)

Organ

Expression



GENE INFORMATION

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Gene name

FGA

Synonyms

Description

Fibrinogen alpha chain (HGNC Symbol)

Entrez gene summary

The protein encoded by this gene is the alpha component of fibrinogen, a blood-borne glycoprotein comprised of three pairs of nonidentical polypeptide chains. Following vascular injury, fibrinogen is cleaved by thrombin to form fibrin which is the most abundant component of blood clots. In addition, various cleavage products of fibrinogen and fibrin regulate cell adhesion and spreading, display vasoconstrictor and chemotactic activities, and are mitogens for several cell types. Mutations in this gene lead to several disorders, including dysfibrinogenemia, hypofibrinogenemia, afibrinogenemia and renal amyloidosis. Alternative splicing results in two isoforms which vary in the carboxy-terminus. [provided by RefSeq, Jul 2008]

Chromosome

4

Cytoband

q31.3

Chromosome location (bp)

154583126 - 154590766

Protein evidence

Evidence at protein level (all genes)

Ensembl

ENSG00000171560 (version 78.38)

Entrez gene

2243

UniProt

P02671 (UniProt - Evidence at protein level)

neXtProt

NX_P02671

Antibodypedia

FGA antibodies


PROTEIN BROWSER

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ENST00000302053
 
ENST00000403106
 
ENST00000622532
 
 
 
 


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)

FGA-001 ENSP00000385981
ENST00000403106
P02671
Show all »
Show » Show » 644 69.8 Yes 0
FGA-002 ENSP00000306361
ENST00000302053
P02671
Show all »
Show » Show » 866 95 Yes 0
FGA-201 ENSP00000478487
ENST00000622532
Q86Z09
Show all »
Show » Show » 289 33 Yes 0