Fibrinogen beta chain

Protein-coding gene in the species Homo sapiens From Wikipedia, the free encyclopedia

Fibrinogen beta chain

Fibrinogen beta chain, also known as FGB, is a gene found in humans and most other vertebrates with a similar system of blood coagulation.

Quick Facts FGB, Available structures ...
FGB
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Available structures
PDBOrtholog search: PDBe RCSB
Identifiers
AliasesFGB, HEL-S-78p, fibrinogen beta chain
External IDsOMIM: 134830; MGI: 99501; HomoloGene: 3772; GeneCards: FGB; OMA:FGB - orthologs
Orthologs
SpeciesHumanMouse
Entrez
Ensembl
UniProt
RefSeq (mRNA)

NM_001184741
NM_005141

NM_181849

RefSeq (protein)

NP_862897

Location (UCSC)Chr 4: 154.56 – 154.57 MbChr 3: 82.95 – 82.96 Mb
PubMed search[3][4]
Wikidata
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The protein encoded by this gene is the beta component of fibrinogen, a blood-borne glycoprotein composed 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 afibrinogenemia, dysfibrinogenemia, hypodysfibrinogenemia and thrombotic tendency.[5]

Interactions

Fibrinogen beta chain has been shown to interact with Lipoprotein(a).[6]

See also


References

Further reading

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