| Selected-GenAtlas references | SOURCE | GeneCards | NCBI Gene | Swiss-Prot | Orphanet | Ensembl |
| HGNC | UniGene | Nucleotide | OMIM | UCSC |
| Home Page |
| FLASH GENE |
| Symbol | FGG | contributors: - updated : 13-10-2007 |
| HGNC name | fibrinogen, G gamma polypeptide |
| HGNC id | 3694 |
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| Corresponding disease |
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| Location | 4q28 Physical location : 155.525.286 - 155.533.902 |
| DNA |
| TYPE | functioning gene |
| SPECIAL FEATURE | component of a cluster |
| text | see FG@ |
| STRUCTURE | 8.00 kb 10 Exon(s) |
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| 10 Kb 5' upstream gene genomic sequence study |
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| MAPPING | cloned | Y | linked | Y | status | confirmed |
| Map | cen - FGG - FGA - FGB - qter |
| Authors | Aschbacher et al.(85) |
Physical map
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| RNA |
| TRANSCRIPTS | type | messenger |
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| EXPRESSION |
| Type | widely |
| constitutive of |
| expressed in | (based on citations) | ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| organ(s) |
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| tissue |
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cell lineage
| cell lines
| fluid/secretion
| plasma | |
| at STAGE |
| physiological period | embryo, fetal |
| Text | liver |
| PROTEIN |
PHYSICAL PROPERTIES
| STRUCTURE
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| conjugated | GlycoP |
| mono polymer | heteromer , hexamer |
| isoforms | Precursor | cleaved by thrombin to form fibrin and various cleavage products of fibrinogen and fibrin |
| HOMOLOGY |
| interspecies | ortholog to murine Fgg |
| homolog to C.elegans C49C8.5 |
| Homologene |
| FAMILY |
| CATEGORY | adhesion , structural protein |
| SUBCELLULAR LOCALIZATION | extracellular |
| text | plasma |
| basic FUNCTION | |
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| CELLULAR PROCESS
| cell life, proliferation/growth |
| PHYSIOLOGICAL PROCESS | coagulation/hemostasis |
| text | positive regulation of cell proliferation |
| PATHWAY |
| metabolism |
| signaling |
| a component | fibrinogen, dimeric protein consisting of six chains (alpha 2, beta 2, gamma 2) held together by disulfide bonds |
| INTERACTION |
| DNA |
| RNA |
| small molecule | metal binding, |
| calcium Ca2+ |
| protein |
| cell & other |
| REGULATION |
| ASSOCIATED DISORDERS |
| corresponding disease(s) | TRDF , CAFG |
| related resource | A Database For Human Fibrinogen Variants |
| Susceptibility | to deep venous thrombosis |
| Variant & Polymorphism SNP | FGG-H2 homozygosity associated with risk of deep venous thrombosis |
Candidate gene
| Marker
| Therapy target
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| ANIMAL & CELL MODELS |