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FGG (fibrinogen gamma chain)

Gene
Entrez ID Entrez Gene ID - the GENE ID in NCBI Gene database.
2266
Gene nameGene Name - the full gene name approved by the HGNC.
Fibrinogen gamma chain
Gene symbolGene Symbol - the official gene symbol approved by the HGNC, which is a short abbreviated form of the gene name.
FGG
SynonymsGene synonyms aliases
-
ChromosomeChromosome number
4
Chromosome locationChromosomal Location - indicates the cytogenetic location of the gene or region on the chromosome.
4q32.1
SummarySummary of gene provided in NCBI Entrez Gene.
The protein encoded by this gene is the gamma 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 ab
SNPsSNP information provided by dbSNP.
SNP ID Visualize variation Clinical significance Consequence
rs6063 C>T Likely-benign, uncertain-significance, pathogenic Coding sequence variant, missense variant
rs78257946 C>T Likely-pathogenic Missense variant, coding sequence variant
rs121913087 G>A Other, pathogenic Missense variant, coding sequence variant
rs121913088 C>T Other, pathogenic Missense variant, coding sequence variant
rs138511699 G>A,C Likely-pathogenic Missense variant, coding sequence variant
miRNAmiRNA information provided by mirtarbase database.
miRTarBase ID miRNA Experiments Reference
MIRT005519 hsa-miR-409-3p ELISA, Flow, Luciferase reporter assay 20570858
MIRT005521 hsa-miR-29a-3p ELISA, Flow, Luciferase reporter assay 20570858
MIRT005522 hsa-miR-29b-3p ELISA, Flow, Luciferase reporter assay 20570858
MIRT005523 hsa-miR-144-3p ELISA, Flow, Luciferase reporter assay 20570858
MIRT005525 hsa-miR-29c-3p Luciferase reporter assay 20570858
Transcription factors
Transcription factor Regulation Reference
STAT3 Activation 11460505
Gene ontology (GO)Gene ontology information of associated ontologies with gene provided by GO database.
GO ID Ontology Definition Evidence Reference
GO:0002224 Process Toll-like receptor signaling pathway TAS
GO:0002576 Process Platelet degranulation TAS
GO:0005102 Function Signaling receptor binding IBA 21873635
GO:0005102 Function Signaling receptor binding IPI 7822297
GO:0005198 Function Structural molecule activity IDA 8910396
Other IDsOther ids provides unique ids of gene in databases such as OMIM, HGNC, ENSEMBLE.
MIM
HGNC
e!Ensembl
Protein
UniProt ID P02679
Protein name Fibrinogen gamma chain
Protein function Together with fibrinogen alpha (FGA) and fibrinogen beta (FGB), polymerizes to form an insoluble fibrin matrix. Has a major function in hemostasis as one of the primary components of blood clots. In addition, functions during the early stages of
PDB 1DUG , 1FIB , 1FIC , 1FID , 1FZA , 1FZB , 1FZC , 1FZE , 1FZF , 1FZG , 1LT9 , 1LTJ , 1N86 , 1N8E , 1RE3 , 1RE4 , 1RF0 , 1RF1 , 2A45 , 2FFD , 2FIB , 2H43 , 2HLO , 2HOD , 2HPC , 2HWL , 2OYH , 2OYI , 2Q9I , 2VDO , 2VDP , 2VDQ , 2VDR , 2VR3 , 2XNX , 2XNY , 2Y7L , 2Z4E , 3BVH , 3E1I , 3FIB , 3GHG , 3H32 , 3HUS , 4B60
Family and domains

Pfam

Accession ID Position in sequence Description Type
PF08702 Fib_alpha
30 172
Fibrinogen alpha/beta chain family
Coiled-coil
PF00147 Fibrinogen_C
175 415
Fibrinogen beta and gamma chains, C-terminal globular domain
Domain
Sequence
Sequence length 453
Interactions View interactions
PathwaysPathway information has different metabolic/signaling pathways associated with genes. Each record is hyperlinked to a complete information page which also includes links to the KEGG/Reactome pathway database.
 
KEGG
 
Reactome
  Complement and coagulation cascades
Platelet activation
Neutrophil extracellular trap formation
Staphylococcus aureus infection
Coronavirus disease - COVID-19
  Platelet degranulation
Common Pathway of Fibrin Clot Formation
Integrin cell surface interactions
Integrin signaling
GRB2:SOS provides linkage to MAPK signaling for Integrins
p130Cas linkage to MAPK signaling for integrins
Regulation of Insulin-like Growth Factor (IGF) transport and uptake by Insulin-like Growth Factor Binding Proteins (IGFBPs)
MAP2K and MAPK activation
Regulation of TLR by endogenous ligand
Signaling by moderate kinase activity BRAF mutants
Signaling by high-kinase activity BRAF mutants
Signaling by BRAF and RAF fusions
Paradoxical activation of RAF signaling by kinase inactive BRAF
Post-translational protein phosphorylation
Signaling downstream of RAS mutants
Associated diseases
Causal
Disease name Disease term dbSNP ID References
Afibrinogenemia Afibrinogenemia, Familial afibrinogenemia rs121913087, rs121909625
Complement component deficiency Complement Factor I (C3 inactivator) deficiency rs387906509, rs1467298230, rs1022194067, rs774370086, rs121964922, rs372345940, rs121913052, rs121913053, rs460897, rs121913054, rs121913056, rs121913058, rs796052138, rs41286844, rs121909592, rs34000044, rs121909594, rs121909587, rs121909588, rs387906554, rs587776846, rs2135727106, rs460184, rs775967055, rs398122811, rs140813121, rs146187042, rs372968576, rs398122867, rs398122868, rs9332736, rs398124644, rs142881576, rs531103546, rs764871530, rs778518669, rs139491301, rs61469168, rs1554718962, rs1565789104, rs1579848888, rs779723422, rs867425110, rs770367814
Congenital afibrinogenemia Congenital hypofibrinogenemia rs121913088, rs587776837, rs587776838, rs587776839, rs121909621, rs121909622, rs606231223, rs606231224, rs121909624, rs121909625, rs146387238, rs606231225, rs755117226, rs1553965519, rs1578810856, rs1578785111, rs1578796476 25427968, 18676163, 11460507, 17295221, 30349899
Dysfibrinogenemia Familial dysfibrinogenemia rs121913087, rs121913088, rs121913091, rs121909606, rs121909607, rs146387238, rs762964798, rs1310452604, rs1578812509, rs1578783532
Unknown
Disease name Disease term dbSNP ID References
Congenital dysfibrinogenemia Dysfibrinogenemia, Congenital 3708159, 15632207, 2257302, 25320241, 2976995, 30349899
Fibrinogen deficiency Fibrinogen Deficiency
Hypodysfibrinogenemia Hypodysfibrinogenemia, Familial hypodysfibrinogenemia
Stomach neoplasms Malignant neoplasm of stomach, Stomach Neoplasms 19424620

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