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.
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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 |
rs148685782 |
G>C |
Likely-benign, pathogenic, likely-pathogenic |
Coding sequence variant, missense variant |
rs587776837 |
C>T |
Pathogenic, likely-pathogenic |
Intron variant |
rs587776838 |
C>T |
Pathogenic |
Intron variant |
rs587776839 |
T>A |
Pathogenic |
Intron variant |
rs587777720 |
A>G |
Pathogenic |
Missense variant, coding sequence variant |
rs1310452604 |
C>A |
Likely-pathogenic |
Missense variant, coding sequence variant |
rs1414035000 |
A>- |
Likely-pathogenic |
Coding sequence variant, frameshift variant |
rs1553965519 |
C>T |
Pathogenic |
Stop gained, coding sequence variant |
rs1560833290 |
C>-,CC |
Likely-pathogenic |
Frameshift variant, coding sequence variant |
rs1578810856 |
A>T |
Pathogenic |
Intron variant |
rs1578812509 |
T>A |
Pathogenic |
Coding sequence variant, stop gained |
|
miRNAmiRNA information provided by mirtarbase database.
|
|
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 |
GO:0005201 |
Function |
Extracellular matrix structural constituent |
HDA |
28344315 |
GO:0005201 |
Function |
Extracellular matrix structural constituent |
RCA |
25037231, 28327460, 28675934 |
GO:0005515 |
Function |
Protein binding |
IPI |
10788510, 21546586, 26627825 |
GO:0005576 |
Component |
Extracellular region |
TAS |
|
GO:0005577 |
Component |
Fibrinogen complex |
IDA |
6451630, 8470043, 8910396, 16846481, 18676163 |
GO:0005615 |
Component |
Extracellular space |
HDA |
16502470 |
GO:0005615 |
Component |
Extracellular space |
IBA |
21873635 |
GO:0005615 |
Component |
Extracellular space |
IDA |
6777381 |
GO:0005788 |
Component |
Endoplasmic reticulum lumen |
TAS |
|
GO:0005886 |
Component |
Plasma membrane |
TAS |
|
GO:0007160 |
Process |
Cell-matrix adhesion |
IBA |
21873635 |
GO:0007160 |
Process |
Cell-matrix adhesion |
IDA |
10903502 |
GO:0007596 |
Process |
Blood coagulation |
TAS |
|
GO:0009306 |
Process |
Protein secretion |
IMP |
18676163 |
GO:0009897 |
Component |
External side of plasma membrane |
IDA |
6777381 |
GO:0009986 |
Component |
Cell surface |
IDA |
6777381 |
GO:0030198 |
Process |
Extracellular matrix organization |
TAS |
|
GO:0031091 |
Component |
Platelet alpha granule |
IDA |
6777381 |
GO:0031093 |
Component |
Platelet alpha granule lumen |
TAS |
|
GO:0031639 |
Process |
Plasminogen activation |
IDA |
16846481 |
GO:0034116 |
Process |
Positive regulation of heterotypic cell-cell adhesion |
IDA |
8100742 |
GO:0034622 |
Process |
Cellular protein-containing complex assembly |
IDA |
8910396 |
GO:0042730 |
Process |
Fibrinolysis |
IDA |
16846481 |
GO:0043687 |
Process |
Post-translational protein modification |
TAS |
|
GO:0044267 |
Process |
Cellular protein metabolic process |
TAS |
|
GO:0045907 |
Process |
Positive regulation of vasoconstriction |
IDA |
15739255 |
GO:0045921 |
Process |
Positive regulation of exocytosis |
IDA |
19193866 |
GO:0046872 |
Function |
Metal ion binding |
IEA |
|
GO:0050714 |
Process |
Positive regulation of protein secretion |
IDA |
19193866 |
GO:0050839 |
Function |
Cell adhesion molecule binding |
IPI |
7822297 |
GO:0051258 |
Process |
Protein polymerization |
IMP |
12706644 |
GO:0051592 |
Process |
Response to calcium ion |
IDA |
6777381 |
GO:0062023 |
Component |
Collagen-containing extracellular matrix |
HDA |
25037231, 28327460, 28344315, 28675934 |
GO:0062023 |
Component |
Collagen-containing extracellular matrix |
IBA |
21873635 |
GO:0070062 |
Component |
Extracellular exosome |
HDA |
19056867, 23533145 |
GO:0070374 |
Process |
Positive regulation of ERK1 and ERK2 cascade |
IDA |
10903502, 19193866 |
GO:0070527 |
Process |
Platelet aggregation |
IBA |
21873635 |
GO:0070527 |
Process |
Platelet aggregation |
IDA |
6281794 |
GO:0072378 |
Process |
Blood coagulation, fibrin clot formation |
IBA |
21873635 |
GO:0072378 |
Process |
Blood coagulation, fibrin clot formation |
IDA |
16846481 |
GO:0072378 |
Process |
Blood coagulation, fibrin clot formation |
IMP |
11001902 |
GO:0072562 |
Component |
Blood microparticle |
HDA |
22516433 |
GO:0090277 |
Process |
Positive regulation of peptide hormone secretion |
IDA |
19193866 |
GO:1900026 |
Process |
Positive regulation of substrate adhesion-dependent cell spreading |
NAS |
24041635 |
GO:1902042 |
Process |
Negative regulation of extrinsic apoptotic signaling pathway via death domain receptors |
IDA |
10903502 |
GO:2000352 |
Process |
Negative regulation of endothelial cell apoptotic process |
IDA |
10903502 |
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Other IDsOther ids provides unique ids of gene in databases such as OMIM, HGNC, ENSEMBLE.
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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.
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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 |
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Gastric cancer |
Hereditary Diffuse Gastric Cancer |
rs137854571, rs63751108, rs34612342, rs121908383, rs121909144, rs121909775, rs121909219, rs121909223, rs63750871, rs80359530, rs121964873, rs121913530, rs606231203, rs121918505, rs587776802, rs28933369, rs121912469, rs80358011, rs397507262, rs80359439, rs397507333, rs80359543, rs80358831, rs80359596, rs80358920, rs80358972, rs80359659, rs397507404, rs397514661, rs80359516, rs200495564, rs80358419, rs80359274, rs80359283, rs80358427, rs80358428, rs80358435, rs81002805, rs397507660, rs397507663, rs80359391, rs80359443, rs81002797, rs80359466, rs397507752, rs80359484, rs80359603, rs397507954, rs80359058, rs80359071, rs397507981, rs80359121, rs80357086, rs80357064, rs397508936, rs80357695, rs80357661, rs397509035, rs80357544, rs80357577, rs80357881, rs80357296, rs80356923, rs80356866, rs80357504, rs80357390, rs80357239, rs80358099, rs397509284, rs80357258, rs199474738, rs199474747, rs587779204, rs63750439, rs267608076, rs587779246, rs63749999, rs267608078, rs63751327, rs267607719, rs267607734, rs63750706, rs63751711, rs587779047, rs587779075, rs267607949, rs63750633, rs63750803, rs63751618, rs267608154, rs200640585, rs80358018, rs80357857, rs80357882, rs180177103, rs587779815, rs587779865, rs587779872, rs587780059, rs121912666, rs587780088, rs587780104, rs200432447, rs180177100, rs587780226, rs587780784, rs587776416, rs587781276, rs587781629, rs587781694, rs587781727, rs587781730, rs587781807, rs587781894, rs587781948, rs121913344, rs587782292, rs587782350, rs587782558, rs587782719, rs587782885, rs587783057, rs730881833, rs730881411, rs730881336, rs139770721, rs730881869, rs730881633, rs730882007, rs786203115, rs765123255, rs1553333738, rs762083530, rs786202800, rs17174393, rs55996097, rs750621215, rs786203451, rs747604569, rs764389018, rs786204433, rs786204862, rs772821016, rs779582317, rs863225406, rs193922343, rs759965045, rs63749919, rs760228510, rs746481984, rs762307622, rs876659736, rs876660933, rs747727055, rs1450394308, rs876658348, rs876658431, rs876659326, rs876660444, rs730881369, rs878853865, rs753862052, rs587780024, rs138941496, rs886040739, rs886040744, rs886040347, rs878854957, rs886040123, rs398122662, rs886040942, rs1057517104, rs1057516320, rs1057516683, rs879254046, rs1057517253, rs587781927, rs985033810, rs1057519989, rs775464903, rs374230313, rs758304323, rs1060501599, rs758081262, rs1060500126, rs1060502734, rs587776408, rs1060501695, rs1114167816, rs1114167596, rs1114167667, rs1555460315, rs1135402788, rs1554086196, rs730881919, rs773356478, rs769237459, rs1553653158, rs587782087, rs1555107263, rs1555119940, rs1403784434, rs1342519012, rs751710099, rs1553616361, rs1553619721, rs1270783041, rs775036118, rs1555288557, rs1555460548, rs1555461154, rs1298667185, rs1553622218, rs63751101, rs1349928568, rs771936821, rs1021662947, rs1555921011, rs81002831, rs1555124506, rs1555574803, rs1060502716, rs1555605362, rs747057367, rs1565385010, rs1567554500, rs1567516230, rs1558644995, rs1555591308, rs778306619, rs1566231194, rs1603328466, rs1570406302, rs1586108714, rs768362387, rs1597713777, rs1060502926, rs1597867185, rs1591517571, rs1591663236, rs1593903006, rs1555284779, rs1597096243, rs45459799, rs1597360340, rs587781905, rs864622481, rs1601753141, rs1966858562, rs1966967065, rs1967016153, rs1967113484, rs2080473458, rs1591387978, rs1224428422, rs1597747184, rs2082309297, rs2051929740, rs147542208 |
19424620 |
Hypofibrinogenemia |
Hypofibrinogenemia, Familial hypofibrinogenemia |
rs121913087, rs121913088, rs587776837, rs121909616, rs121909625, rs121909608, rs121909607, rs146387238, rs1578795296, rs1214070111, rs776817952, rs762964798, rs121909606, rs1414035000, rs1310452604 |
31064749 |
|
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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