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Fusion gene ID: 13431 |
FusionGeneSummary for FGG_CLCN3 |
 Fusion gene summary |
| Fusion gene information | Fusion gene name: FGG_CLCN3 | Fusion gene ID: 13431 | Hgene | Tgene | Gene symbol | FGG | CLCN3 | Gene ID | 2266 | 1182 |
| Gene name | fibrinogen gamma chain | chloride voltage-gated channel 3 | |
| Synonyms | - | CLC3|ClC-3 | |
| Cytomap | 4q32.1 | 4q33 | |
| Type of gene | protein-coding | protein-coding | |
| Description | fibrinogen gamma chainfibrinogen, gamma polypeptidetesticular tissue protein Li 70 | H(+)/Cl(-) exchange transporter 3chloride channel 3chloride channel protein 3chloride channel, voltage-sensitive 3chloride transporter ClC-3 | |
| Modification date | 20180519 | 20180523 | |
| UniProtAcc | P02679 | P51790 | |
| Ensembl transtripts involved in fusion gene | ENST00000404648, ENST00000405164, ENST00000336098, ENST00000407946, | ENST00000513761, ENST00000347613, ENST00000360642, ENST00000504131, ENST00000506924, | |
| Fusion gene scores | * DoF score | 4 X 4 X 2=32 | 36 X 4 X 19=2736 |
| # samples | 4 | 39 | |
| ** MAII score | log2(4/32*10)=0.321928094887362 effective Gene in Pan-Cancer Fusion Genes (eGinPCFGs). DoF>8 and MAII>0 | log2(39/2736*10)=-2.81052220113629 possibly effective Gene in Pan-Cancer Fusion Genes (peGinPCFGs). DoF>8 and MAII<0 | |
| Context | PubMed: FGG [Title/Abstract] AND CLCN3 [Title/Abstract] AND fusion [Title/Abstract] | ||
| Functional or gene categories assigned by FusionGDB annotation | |||
| * DoF score (Degree of Frequency) = # partners X # break points X # cancer types ** MAII score (Major Active Isofusion Index) = log2(# samples/DoF score*10) |
| Gene ontology of each fusion partner gene with evidence of Inferred from Direct Assay (IDA) from Entrez |
| Partner | Gene | GO ID | GO term | PubMed ID |
| Hgene | FGG | GO:0007160 | cell-matrix adhesion | 10903502 |
| Hgene | FGG | GO:0031639 | plasminogen activation | 16846481 |
| Hgene | FGG | GO:0034116 | positive regulation of heterotypic cell-cell adhesion | 8100742 |
| Hgene | FGG | GO:0034622 | cellular protein-containing complex assembly | 8910396 |
| Hgene | FGG | GO:0042730 | fibrinolysis | 16846481 |
| Hgene | FGG | GO:0045907 | positive regulation of vasoconstriction | 15739255 |
| Hgene | FGG | GO:0045921 | positive regulation of exocytosis | 19193866 |
| Hgene | FGG | GO:0050714 | positive regulation of protein secretion | 19193866 |
| Hgene | FGG | GO:0051592 | response to calcium ion | 6777381 |
| Hgene | FGG | GO:0070374 | positive regulation of ERK1 and ERK2 cascade | 10903502|19193866 |
| Hgene | FGG | GO:0070527 | platelet aggregation | 6281794 |
| Hgene | FGG | GO:0072378 | blood coagulation, fibrin clot formation | 16846481 |
| Hgene | FGG | GO:0090277 | positive regulation of peptide hormone secretion | 19193866 |
| Hgene | FGG | GO:1902042 | negative regulation of extrinsic apoptotic signaling pathway via death domain receptors | 10903502 |
| Hgene | FGG | GO:2000352 | negative regulation of endothelial cell apoptotic process | 10903502 |
| Tgene | CLCN3 | GO:1902476 | chloride transmembrane transport | 11274166 |
| Fusion gene information from three resources (ChiTars (NAR, 2018), tumorfusions (NAR, 2018), Gao et al. (Cell, 2018)) * All genome coordinats were lifted-over on hg19. * Click on the break point to see the gene structure around the break point region using the UCSC Genome Browser. |
| Data type | Source | Cancer type | Sample | Hgene | Hchr | Hbp | Hstrand | Tgene | Tchr | Tbp | Tstrand |
| TCGA | RV | LIHC | TCGA-DD-AADQ-01A | FGG | chr4 | 155525286 | - | CLCN3 | chr4 | 170623929 | + |
| * LD: Li Ding group's fusion gene list RV: Roel Verhaak group's fusion gene list ChiTaRs fusion database |
| Open reading frame (ORF) analsis of fusion genes based on Ensembl gene isoform structure. * Click on the break point to see the gene structure around the break point region using the UCSC Genome Browser. |
| ORF | Henst | Tenst | Hgene | Hchr | Hbp | Hstrand | Tgene | Tchr | Tbp | Tstrand |
| 5CDS-intron | ENST00000404648 | ENST00000513761 | FGG | chr4 | 155525286 | - | CLCN3 | chr4 | 170623929 | + |
| 5CDS-intron | ENST00000404648 | ENST00000347613 | FGG | chr4 | 155525286 | - | CLCN3 | chr4 | 170623929 | + |
| 5CDS-intron | ENST00000404648 | ENST00000360642 | FGG | chr4 | 155525286 | - | CLCN3 | chr4 | 170623929 | + |
| 5CDS-intron | ENST00000404648 | ENST00000504131 | FGG | chr4 | 155525286 | - | CLCN3 | chr4 | 170623929 | + |
| 5CDS-intron | ENST00000404648 | ENST00000506924 | FGG | chr4 | 155525286 | - | CLCN3 | chr4 | 170623929 | + |
| intron-intron | ENST00000405164 | ENST00000513761 | FGG | chr4 | 155525286 | - | CLCN3 | chr4 | 170623929 | + |
| intron-intron | ENST00000405164 | ENST00000347613 | FGG | chr4 | 155525286 | - | CLCN3 | chr4 | 170623929 | + |
| intron-intron | ENST00000405164 | ENST00000360642 | FGG | chr4 | 155525286 | - | CLCN3 | chr4 | 170623929 | + |
| intron-intron | ENST00000405164 | ENST00000504131 | FGG | chr4 | 155525286 | - | CLCN3 | chr4 | 170623929 | + |
| intron-intron | ENST00000405164 | ENST00000506924 | FGG | chr4 | 155525286 | - | CLCN3 | chr4 | 170623929 | + |
| intron-intron | ENST00000336098 | ENST00000513761 | FGG | chr4 | 155525286 | - | CLCN3 | chr4 | 170623929 | + |
| intron-intron | ENST00000336098 | ENST00000347613 | FGG | chr4 | 155525286 | - | CLCN3 | chr4 | 170623929 | + |
| intron-intron | ENST00000336098 | ENST00000360642 | FGG | chr4 | 155525286 | - | CLCN3 | chr4 | 170623929 | + |
| intron-intron | ENST00000336098 | ENST00000504131 | FGG | chr4 | 155525286 | - | CLCN3 | chr4 | 170623929 | + |
| intron-intron | ENST00000336098 | ENST00000506924 | FGG | chr4 | 155525286 | - | CLCN3 | chr4 | 170623929 | + |
| intron-intron | ENST00000407946 | ENST00000513761 | FGG | chr4 | 155525286 | - | CLCN3 | chr4 | 170623929 | + |
| intron-intron | ENST00000407946 | ENST00000347613 | FGG | chr4 | 155525286 | - | CLCN3 | chr4 | 170623929 | + |
| intron-intron | ENST00000407946 | ENST00000360642 | FGG | chr4 | 155525286 | - | CLCN3 | chr4 | 170623929 | + |
| intron-intron | ENST00000407946 | ENST00000504131 | FGG | chr4 | 155525286 | - | CLCN3 | chr4 | 170623929 | + |
| intron-intron | ENST00000407946 | ENST00000506924 | FGG | chr4 | 155525286 | - | CLCN3 | chr4 | 170623929 | + |
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FusionProtFeatures for FGG_CLCN3 |
| Main function of each fusion partner protein. (from UniProt) |
| Hgene | Tgene |
| FGG | CLCN3 |
| Mediates the exchange of chloride ions against protons.Functions as antiporter and contributes to the acidification ofthe endosome and synaptic vesicle lumen, and may thereby affectvesicle trafficking and exocytosis. May play an important role inneuronal cell function through regulation of membrane excitabilityby protein kinase C. It could help neuronal cells to establishshort-term memory. {ECO:0000269|PubMed:11967229}. |
| Retention analysis result of each fusion partner protein across 39 protein features of UniProt such as six molecule processing features, 13 region features, four site features, six amino acid modification features, two natural variation features, five experimental info features, and 3 secondary structure features. Here, because of limited space for viewing, we only show the protein feature retention information belong to the 13 regional features. All retention annotation result can be downloaded at . * Minus value of BPloci means that the break pointn is located before the CDS. |
| - In-frame and retained protein feature among the 13 regional features. |
| Partner | Gene | Hbp | Tbp | ENST | Strand | BPexon | TotalExon | Protein feature loci | *BPloci | TotalLen | Protein feature | Protein feature note |
| - In-frame and not-retained protein feature among the 13 regional features. |
| Partner | Gene | Hbp | Tbp | ENST | Strand | BPexon | TotalExon | Protein feature loci | *BPloci | TotalLen | Protein feature | Protein feature note |
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FusionGeneSequence for FGG_CLCN3 |
| For in-frame fusion transcripts, we provide the fusion transcript sequences and fusion amino acid sequences. (nt: nucleotides, aa: amino acids) |
| * Fusion amino acid sequences. |
| * Fusion transcript sequences (only coding sequence (CDS) region). |
| * Fusion transcript sequences (Full-length transcript). |
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FusionGenePPI for FGG_CLCN3 |
| Go to ChiPPI (Chimeric Protein-Protein interactions) to see the chimeric PPI interaction in . |
| Protein-protein interactors with each fusion partner protein in wild-type (BIOGRID-3.4.160) |
| Hgene | Hgene's interactors | Tgene | Tgene's interactors |
| FGG | FGA, FGB, F13B, FGG, KHDRBS2, VKORC1, FN1, ASB6, ASB7, ASB12, CA8, ASCC1, DDX19B, ALDH2, CHD9, NUP93, ICAM1, HIST1H2BJ, MAPK6, RING1, SNX27, CDK15, CCNYL1 | CLCN3 | CLCN3, SLC9A3R1, PDZK1, GOPC, CFTR, LGALS3, LGALS8, LGALS9, LYPD3, HSPB1, TMEM9B, GGA1, TPCN2, TRIM25 |
| - Retained PPIs in in-frame fusion. |
| Partner | Gene | Hbp | Tbp | ENST | Strand | BPexon | TotalExon | Protein feature loci | *BPloci | TotalLen | Still interaction with |
| - Lost PPIs in in-frame fusion. |
| Partner | Gene | Hbp | Tbp | ENST | Strand | BPexon | TotalExon | Protein feature loci | *BPloci | TotalLen | Interaction lost with |
| - Retained PPIs, but lost function due to frame-shift fusion. |
| Partner | Gene | Hbp | Tbp | ENST | Strand | BPexon | TotalExon | Protein feature loci | *BPloci | TotalLen | Interaction lost with |
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RelatedDrugs for FGG_CLCN3 |
| Drugs targeting genes involved in this fusion gene. (DrugBank Version 5.1.0 2018-04-02) |
| Partner | Gene | UniProtAcc | DrugBank ID | Drug name | Drug activity | Drug type | Drug status |
| Hgene | FGG | P02679 | DB00364 | Sucralfate | Fibrinogen gamma chain | small molecule | approved |
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RelatedDiseases for FGG_CLCN3 |
| Diseases associated with fusion partners. (DisGeNet 4.0) |
| Partner | Gene | Disease ID | Disease name | # pubmeds | Source |
| Hgene | FGG | C0272350 | Dysfibrinogenemia, Congenital | 7 | ORPHANET;UNIPROT |
| Hgene | FGG | C0022548 | Keloid | 1 | CTD_human |
| Hgene | FGG | C0038356 | Stomach Neoplasms | 1 | CTD_human |
| Hgene | FGG | C2584774 | Congenital hypofibrinogenemia | 1 | ORPHANET;UNIPROT |
| Tgene | CLCN3 | C0017638 | Glioma | 1 | CTD_human |
| Tgene | CLCN3 | C0038356 | Stomach Neoplasms | 1 | CTD_human |
| Tgene | CLCN3 | C2931822 | Nasopharyngeal carcinoma | 1 | CTD_human |
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