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Fusion gene ID: 27707 |
FusionGeneSummary for PLRG1_FGG |
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Fusion gene information | Fusion gene name: PLRG1_FGG | Fusion gene ID: 27707 | Hgene | Tgene | Gene symbol | PLRG1 | FGG | Gene ID | 5356 | 2266 |
Gene name | pleiotropic regulator 1 | fibrinogen gamma chain | |
Synonyms | Cwc1|PRL1|PRP46|PRPF46|TANGO4 | - | |
Cytomap | 4q31.3 | 4q32.1 | |
Type of gene | protein-coding | protein-coding | |
Description | pleiotropic regulator 1pleiotropic regulator 1 (PRL1 homolog, Arabidopsis)transport and golgi organization 4 homolog | fibrinogen gamma chainfibrinogen, gamma polypeptidetesticular tissue protein Li 70 | |
Modification date | 20180523 | 20180519 | |
UniProtAcc | O43660 | P02679 | |
Ensembl transtripts involved in fusion gene | ENST00000499023, ENST00000393905, ENST00000302078, | ENST00000404648, ENST00000405164, ENST00000336098, ENST00000407946, | |
Fusion gene scores | * DoF score | 2 X 3 X 2=12 | 8 X 9 X 3=216 |
# samples | 3 | 14 | |
** MAII score | log2(3/12*10)=1.32192809488736 effective Gene in Pan-Cancer Fusion Genes (eGinPCFGs). DoF>8 and MAII>0 | log2(14/216*10)=-0.625604485218502 possibly effective Gene in Pan-Cancer Fusion Genes (peGinPCFGs). DoF>8 and MAII<0 | |
Context | PubMed: PLRG1 [Title/Abstract] AND FGG [Title/Abstract] AND fusion [Title/Abstract] | ||
Functional or gene categories assigned by FusionGDB annotation | DDR (DNA damage repair) gene involved fusion gene, retained protein feature but frameshift. |
* DoF score (Degree of Frequency) = # partners X # break points X # cancer types ** MAII score (Major Active Isofusion Index) = log2(# samples/DoF score*10) |
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Partner | Gene | GO ID | GO term | PubMed ID |
Hgene | PLRG1 | GO:0000398 | mRNA splicing, via spliceosome | 28076346 |
Tgene | FGG | GO:0007160 | cell-matrix adhesion | 10903502 |
Tgene | FGG | GO:0031639 | plasminogen activation | 16846481 |
Tgene | FGG | GO:0034116 | positive regulation of heterotypic cell-cell adhesion | 8100742 |
Tgene | FGG | GO:0034622 | cellular protein-containing complex assembly | 8910396 |
Tgene | FGG | GO:0042730 | fibrinolysis | 16846481 |
Tgene | FGG | GO:0045907 | positive regulation of vasoconstriction | 15739255 |
Tgene | FGG | GO:0045921 | positive regulation of exocytosis | 19193866 |
Tgene | FGG | GO:0050714 | positive regulation of protein secretion | 19193866 |
Tgene | FGG | GO:0051592 | response to calcium ion | 6777381 |
Tgene | FGG | GO:0070374 | positive regulation of ERK1 and ERK2 cascade | 10903502|19193866 |
Tgene | FGG | GO:0070527 | platelet aggregation | 6281794 |
Tgene | FGG | GO:0072378 | blood coagulation, fibrin clot formation | 16846481 |
Tgene | FGG | GO:0090277 | positive regulation of peptide hormone secretion | 19193866 |
Tgene | FGG | GO:1902042 | negative regulation of extrinsic apoptotic signaling pathway via death domain receptors | 10903502 |
Tgene | FGG | GO:2000352 | negative regulation of endothelial cell apoptotic process | 10903502 |
![]() (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 | LD | LIHC | TCGA-ED-A459-01A | PLRG1 | chr4 | 155466988 | - | FGG | chr4 | 155525506 | - |
TCGA | LD | LIHC | TCGA-HP-A5MZ-01A | PLRG1 | chr4 | 155465597 | - | FGG | chr4 | 155528134 | - |
* LD: Li Ding group's fusion gene list RV: Roel Verhaak group's fusion gene list ChiTaRs fusion database |
![]() * 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 |
Frame-shift | ENST00000499023 | ENST00000404648 | PLRG1 | chr4 | 155466988 | - | FGG | chr4 | 155525506 | - |
In-frame | ENST00000499023 | ENST00000405164 | PLRG1 | chr4 | 155466988 | - | FGG | chr4 | 155525506 | - |
5CDS-intron | ENST00000499023 | ENST00000336098 | PLRG1 | chr4 | 155466988 | - | FGG | chr4 | 155525506 | - |
5CDS-intron | ENST00000499023 | ENST00000407946 | PLRG1 | chr4 | 155466988 | - | FGG | chr4 | 155525506 | - |
Frame-shift | ENST00000393905 | ENST00000404648 | PLRG1 | chr4 | 155466988 | - | FGG | chr4 | 155525506 | - |
In-frame | ENST00000393905 | ENST00000405164 | PLRG1 | chr4 | 155466988 | - | FGG | chr4 | 155525506 | - |
5CDS-intron | ENST00000393905 | ENST00000336098 | PLRG1 | chr4 | 155466988 | - | FGG | chr4 | 155525506 | - |
5CDS-intron | ENST00000393905 | ENST00000407946 | PLRG1 | chr4 | 155466988 | - | FGG | chr4 | 155525506 | - |
Frame-shift | ENST00000302078 | ENST00000404648 | PLRG1 | chr4 | 155466988 | - | FGG | chr4 | 155525506 | - |
In-frame | ENST00000302078 | ENST00000405164 | PLRG1 | chr4 | 155466988 | - | FGG | chr4 | 155525506 | - |
5CDS-intron | ENST00000302078 | ENST00000336098 | PLRG1 | chr4 | 155466988 | - | FGG | chr4 | 155525506 | - |
5CDS-intron | ENST00000302078 | ENST00000407946 | PLRG1 | chr4 | 155466988 | - | FGG | chr4 | 155525506 | - |
Frame-shift | ENST00000499023 | ENST00000404648 | PLRG1 | chr4 | 155465597 | - | FGG | chr4 | 155528134 | - |
Frame-shift | ENST00000499023 | ENST00000405164 | PLRG1 | chr4 | 155465597 | - | FGG | chr4 | 155528134 | - |
Frame-shift | ENST00000499023 | ENST00000336098 | PLRG1 | chr4 | 155465597 | - | FGG | chr4 | 155528134 | - |
Frame-shift | ENST00000499023 | ENST00000407946 | PLRG1 | chr4 | 155465597 | - | FGG | chr4 | 155528134 | - |
Frame-shift | ENST00000393905 | ENST00000404648 | PLRG1 | chr4 | 155465597 | - | FGG | chr4 | 155528134 | - |
Frame-shift | ENST00000393905 | ENST00000405164 | PLRG1 | chr4 | 155465597 | - | FGG | chr4 | 155528134 | - |
Frame-shift | ENST00000393905 | ENST00000336098 | PLRG1 | chr4 | 155465597 | - | FGG | chr4 | 155528134 | - |
Frame-shift | ENST00000393905 | ENST00000407946 | PLRG1 | chr4 | 155465597 | - | FGG | chr4 | 155528134 | - |
Frame-shift | ENST00000302078 | ENST00000404648 | PLRG1 | chr4 | 155465597 | - | FGG | chr4 | 155528134 | - |
Frame-shift | ENST00000302078 | ENST00000405164 | PLRG1 | chr4 | 155465597 | - | FGG | chr4 | 155528134 | - |
Frame-shift | ENST00000302078 | ENST00000336098 | PLRG1 | chr4 | 155465597 | - | FGG | chr4 | 155528134 | - |
Frame-shift | ENST00000302078 | ENST00000407946 | PLRG1 | chr4 | 155465597 | - | FGG | chr4 | 155528134 | - |
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FusionProtFeatures for PLRG1_FGG |
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Hgene | Tgene |
PLRG1 | FGG |
Involved in pre-mRNA splicing as component of thespliceosome (PubMed:28502770, PubMed:28076346). Component of thePRP19-CDC5L complex that forms an integral part of the spliceosomeand is required for activating pre-mRNA splicing (PubMed:11101529,PubMed:11544257). {ECO:0000269|PubMed:11101529,ECO:0000269|PubMed:11544257, ECO:0000269|PubMed:28076346,ECO:0000269|PubMed:28502770}. |
![]() * 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 PLRG1_FGG |
![]() (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 PLRG1_FGG |
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Hgene | Hgene's interactors | Tgene | Tgene's interactors |
PLRG1 | PRPF19, CDC5L, BCAS2, CPVL, USP42, ZSCAN1, SRRM1, CTNNBL1, KPNA2, KPNA1, TADA2A, SF3A2, CUL3, U2AF2, CWC15, USB1, APP, PRPF4, XAB2, RBM39, ISY1, SNRPA1, SF3A1, ZCRB1, RBM14, UCHL5, RPL9, MDC1, EIF4A3, MAGOH, SF3B1, CSNK2A2, SUZ12, BMI1, CCDC94, HNRNPM, NTRK1, AP2M1, ISY1-RAB43, MRPL40, PDIA5, PABPC1, PABPC4, PCF11, PRPF3, PRPF8, SF3A3, SF3B3, SNRPD2, SNW1, MX1, SCARNA22, IFI16, XPO1, BACH1, LINS, CWF19L2, CRNKL1, AQR, DHX35, GPATCH1, SYF2, PPIE, AAR2, CD2BP2, EAPP, TSSC4, DLST, PDHA1, RNF157 | FGG | FGA, FGB, F13B, FGG, KHDRBS2, VKORC1, FN1, ASB6, ASB7, ASB12, CA8, ASCC1, DDX19B, ALDH2, CHD9, NUP93, ICAM1, HIST1H2BJ, MAPK6, RING1, SNX27, CDK15, CCNYL1 |
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Partner | Gene | Hbp | Tbp | ENST | Strand | BPexon | TotalExon | Protein feature loci | *BPloci | TotalLen | Still interaction with |
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Partner | Gene | Hbp | Tbp | ENST | Strand | BPexon | TotalExon | Protein feature loci | *BPloci | TotalLen | Interaction lost with |
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Partner | Gene | Hbp | Tbp | ENST | Strand | BPexon | TotalExon | Protein feature loci | *BPloci | TotalLen | Interaction lost with |
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RelatedDrugs for PLRG1_FGG |
![]() (DrugBank Version 5.1.0 2018-04-02) |
Partner | Gene | UniProtAcc | DrugBank ID | Drug name | Drug activity | Drug type | Drug status |
Tgene | FGG | P02679 | DB00364 | Sucralfate | Fibrinogen gamma chain | small molecule | approved |
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RelatedDiseases for PLRG1_FGG |
![]() (DisGeNet 4.0) |
Partner | Gene | Disease ID | Disease name | # pubmeds | Source |
Tgene | FGG | C0272350 | Dysfibrinogenemia, Congenital | 7 | ORPHANET;UNIPROT |
Tgene | FGG | C0022548 | Keloid | 1 | CTD_human |
Tgene | FGG | C0038356 | Stomach Neoplasms | 1 | CTD_human |
Tgene | FGG | C2584774 | Congenital hypofibrinogenemia | 1 | ORPHANET;UNIPROT |