| Selected-GenAtlas references | SOURCE | GeneCards | NCBI Gene | Swiss-Prot | Orphanet | Ensembl |
| HGNC | UniGene | Nucleotide | OMIM | UCSC |
| Home Page |
| FLASH GENE |
| Symbol | FGA | contributors: npt/ - updated : 24-04-2006 |
| HGNC name | fibrinogen alpha chain |
| HGNC id | 3661 |
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| Corresponding disease |
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| Location | 4q32.1 Physical location : 155.504.279 - 155.511.897 | ||||||
| Synonym name | |||||||
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| Synonym symbol(s) | Fib2, MGC119422, MGC119423, MGC119425 |
| DNA |
| TYPE | functioning gene |
| SPECIAL FEATURE | component of a cluster |
| text | see FG@ |
| STRUCTURE | 7.62 kb 6 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 (1985) |
Physical map
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| RNA |
| TRANSCRIPTS | type | messenger |
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| EXPRESSION |
| Type | restricted |
| constitutive of |
| expressed in | (based on citations) | ||||||||||||||||||||||||||||||
| organ(s) |
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| tissue |
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cell lineage
| cell lines
| fluid/secretion
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| at STAGE |
| physiological period | fetal |
| Text | liver |
| IMPRINTING | paternally |
| text | paternally imprinted in any cases of a fibrinogenemia |
| PROTEIN |
PHYSICAL PROPERTIES
| STRUCTURE
| |
| isoforms | Precursor | cleaved by thrombin in the N terminal region |
| HOMOLOGY |
| Homologene |
| FAMILY |
| CATEGORY | structural protein |
| SUBCELLULAR LOCALIZATION | extracellular |
| text | plasma |
| basic FUNCTION |
| CELLULAR PROCESS |
| PHYSIOLOGICAL PROCESS | coagulation/hemostasis |
| PATHWAY |
| metabolism |
| signaling |
| a component |
| INTERACTION |
| DNA |
| RNA |
| small molecule |
| protein |
| cell & other |
| REGULATION |
| ASSOCIATED DISORDERS |
| corresponding disease(s) | FAMYR1 , CAFG , TRDF |
| related resource | A Database For Human Fibrinogen Variants |
| Susceptibility | to venous thromboembolism |
| Variant & Polymorphism other | polymorphism associated to venous thromboembolism |
Candidate gene
| Marker
| Therapy target
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| ANIMAL & CELL MODELS |