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Center for Computational Systems Medicine
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FusionGeneSummary

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FusionProtFeature

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FusionGeneSequence

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FusionGenePPI

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RelatedDrugs

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RelatedDiseases

Fusion gene ID: 28984

FusionGeneSummary for PRRC2C_FASLG

check button Fusion gene summary
Fusion gene informationFusion gene name: PRRC2C_FASLG
Fusion gene ID: 28984
HgeneTgene
Gene symbol

PRRC2C

FASLG

Gene ID

23215

356

Gene nameproline rich coiled-coil 2CFas ligand
SynonymsBAT2-iso|BAT2D1|BAT2L2|XTP2ALPS1B|APT1LG1|APTL|CD178|CD95-L|CD95L|FASL|TNFSF6|TNLG1A
Cytomap

1q24.3

1q24.3

Type of geneprotein-codingprotein-coding
Descriptionprotein PRRC2CBAT2 domain containing 1BAT2 domain-containing protein 1HBV X-transactivated gene 2 proteinHBV XAg-transactivated protein 2HBxAg transactivated protein 2HLA-B-associated transcript 2-like 2proline-rich and coiled-coil-containing protetumor necrosis factor ligand superfamily member 6CD95 ligandFas ligand (TNF superfamily, member 6)apoptosis (APO-1) antigen ligand 1apoptosis antigen ligandfas antigen ligandmutant tumor necrosis factor family member 6tumor necrosis factor ligand 1
Modification date2018052320180522
UniProtAcc

Q9Y520

P48023

Ensembl transtripts involved in fusion geneENST00000426496, ENST00000392078, 
ENST00000476522, ENST00000367742, 
ENST00000338920, 
ENST00000340030, 
ENST00000367721, 
Fusion gene scores* DoF score12 X 13 X 5=7801 X 1 X 1=1
# samples 171
** MAII scorelog2(17/780*10)=-2.19793937761191
possibly effective Gene in Pan-Cancer Fusion Genes (peGinPCFGs).
DoF>8 and MAII<0
log2(1/1*10)=3.32192809488736
Context

PubMed: PRRC2C [Title/Abstract] AND FASLG [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)

check button Gene ontology of each fusion partner gene with evidence of Inferred from Direct Assay (IDA) from Entrez
PartnerGeneGO IDGO termPubMed ID
TgeneFASLG

GO:0000122

negative regulation of transcription by RNA polymerase II

17557115

TgeneFASLG

GO:0008625

extrinsic apoptotic signaling pathway via death domain receptors

18835034|26582200

TgeneFASLG

GO:0016525

negative regulation of angiogenesis

18835034

TgeneFASLG

GO:0043065

positive regulation of apoptotic process

14749367|21625644

TgeneFASLG

GO:0070231

T cell apoptotic process

17076679

TgeneFASLG

GO:0070266

necroptotic process

11101870

TgeneFASLG

GO:0097190

apoptotic signaling pathway

11101870

TgeneFASLG

GO:0097191

extrinsic apoptotic signaling pathway

22891283

TgeneFASLG

GO:0097527

necroptotic signaling pathway

11101870

TgeneFASLG

GO:1903514

release of sequestered calcium ion into cytosol by endoplasmic reticulum

26582200

TgeneFASLG

GO:2000353

positive regulation of endothelial cell apoptotic process

18835034


check button 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 typeSourceCancer typeSampleHgeneHchrHbpHstrandTgeneTchrTbpTstrand
TCGALDBRCATCGA-A7-A0CG-01APRRC2Cchr1

171454874

+FASLGchr1

172634762

+
* LD: Li Ding group's fusion gene list
  RV: Roel Verhaak group's fusion gene list
  ChiTaRs fusion database

check button 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.
ORFHenstTenstHgeneHchrHbpHstrandTgeneTchrTbpTstrand
5UTR-3UTRENST00000426496ENST00000340030PRRC2Cchr1

171454874

+FASLGchr1

172634762

+
5UTR-3UTRENST00000426496ENST00000367721PRRC2Cchr1

171454874

+FASLGchr1

172634762

+
5UTR-3UTRENST00000392078ENST00000340030PRRC2Cchr1

171454874

+FASLGchr1

172634762

+
5UTR-3UTRENST00000392078ENST00000367721PRRC2Cchr1

171454874

+FASLGchr1

172634762

+
3UTR-3UTRENST00000476522ENST00000340030PRRC2Cchr1

171454874

+FASLGchr1

172634762

+
3UTR-3UTRENST00000476522ENST00000367721PRRC2Cchr1

171454874

+FASLGchr1

172634762

+
5UTR-3UTRENST00000367742ENST00000340030PRRC2Cchr1

171454874

+FASLGchr1

172634762

+
5UTR-3UTRENST00000367742ENST00000367721PRRC2Cchr1

171454874

+FASLGchr1

172634762

+
5UTR-3UTRENST00000338920ENST00000340030PRRC2Cchr1

171454874

+FASLGchr1

172634762

+
5UTR-3UTRENST00000338920ENST00000367721PRRC2Cchr1

171454874

+FASLGchr1

172634762

+

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FusionProtFeatures for PRRC2C_FASLG


check buttonMain function of each fusion partner protein. (from UniProt)
HgeneTgene
PRRC2C

Q9Y520

FASLG

P48023

Cytokine that binds to TNFRSF6/FAS, a receptor thattransduces the apoptotic signal into cells (PubMed:26334989,PubMed:9228058). Involved in cytotoxic T-cell-mediated apoptosis,natural killer cell-mediated apoptosis and in T-cell development(PubMed:9228058, PubMed:7528780, PubMed:9427603). Initiatesfratricidal/suicidal activation-induced cell death (AICD) inantigen-activated T-cells contributing to the termination ofimmune responses (By similarity). TNFRSF6/FAS-mediated apoptosishas also a role in the induction of peripheral tolerance (Bysimilarity). Binds to TNFRSF6B/DcR3, a decoy receptor that blocksapoptosis (PubMed:27806260). {ECO:0000250|UniProtKB:P41047,ECO:0000269|PubMed:17557115, ECO:0000269|PubMed:27806260,ECO:0000269|PubMed:7528780, ECO:0000269|PubMed:9228058,ECO:0000269|PubMed:9427603}. Tumor necrosis factor ligand superfamily member 6,soluble form: Induces FAS-mediated activation of NF-kappa-B,initiating non-apoptotic signaling pathways (By similarity). Caninduce apoptosis but does not appear to be essential for thisprocess (PubMed:27806260). {ECO:0000250|UniProtKB:P41047,ECO:0000269|PubMed:27806260}. FasL intracellular domain: Cytoplasmic form induces genetranscription inhibition. {ECO:0000269|PubMed:17557115}.

check buttonRetention 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

download page

.

* 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.
PartnerGeneHbpTbpENSTStrandBPexonTotalExonProtein feature loci*BPlociTotalLenProtein featureProtein feature note

- In-frame and not-retained protein feature among the 13 regional features.
PartnerGeneHbpTbpENSTStrandBPexonTotalExonProtein feature loci*BPlociTotalLenProtein featureProtein feature note


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FusionGeneSequence for PRRC2C_FASLG


check button 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 PRRC2C_FASLG


check button Go to ChiPPI (Chimeric Protein-Protein interactions) to see the chimeric PPI interaction in

ChiPPI page

.

check button Protein-protein interactors with each fusion partner protein in wild-type (BIOGRID-3.4.160)
HgeneHgene's interactorsTgeneTgene's interactors
PRRC2CELAVL1, SIRT7, HINFP, ITGA4, TARDBP, PARK2, LGR4, CSNK2A2, SHFM1, AURKA, AURKB, CEP57, HAUS2, CEP76, LGALS3BP, TP53, QPRT, FBL, RABGGTB, PRMT8, ZFP41, NTRK1, SRPK2, RPL10, C10orf12, FOXK2, ATOH1, JPH4, SNRNP70, CHCHD10, TRPC4AP, SFPQ, CYLD, TRIM25, G3BP1FASLGTNFRSF10B, BID, EZR, FADD, FAS, MAPK8, MSN, CASP10, CASP8, RHOA, ARHGDIA, TNFRSF1A, FNBP1, PACSIN2, GRB2, FN1, MMP7, TNFRSF6B, FYN, LCK, GRAP, GRAP2, NCK1, PTPN13, FGR, LYN, ITSN2, PPIAP11, OSTF1, SNX33, HCK, YES1, SRC, SNX9, SRGAP1, SH3PXD2B, BTK, EPS8L3, ARHGAP9, MYO15A, NCK2, FYB, TEC, SPTA1, SAMSN1, SH3RF2, DLG2, SORBS3, SKAP2, CRK, NCKIPSD, SH3PXD2A, BAIAP2L1, SH3GL3, TJP3, CACNB3, MPP4, PIK3CA, DNMBP, DOCK4, KALRN, MACC1, SRGAP3, MIA, SRGAP2, NCF1, ITK, CACNB4, RIMBP3C, SNX18, CFLAR, TRIP6, RGS20, KRT40, NOTCH2NL, CLPX, P3H4, PRMT2, EIF2AK1, LEPREL2, MOSPD2, PIK3R1


check button - Retained PPIs in in-frame fusion.
PartnerGeneHbpTbpENSTStrandBPexonTotalExonProtein feature loci*BPlociTotalLenStill interaction with


check button - Lost PPIs in in-frame fusion.
PartnerGeneHbpTbpENSTStrandBPexonTotalExonProtein feature loci*BPlociTotalLenInteraction lost with


check button - Retained PPIs, but lost function due to frame-shift fusion.
PartnerGeneHbpTbpENSTStrandBPexonTotalExonProtein feature loci*BPlociTotalLenInteraction lost with


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RelatedDrugs for PRRC2C_FASLG


check button Drugs targeting genes involved in this fusion gene.
(DrugBank Version 5.1.0 2018-04-02)
PartnerGeneUniProtAccDrugBank IDDrug nameDrug activityDrug typeDrug status

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RelatedDiseases for PRRC2C_FASLG


check button Diseases associated with fusion partners.
(DisGeNet 4.0)
PartnerGeneDisease IDDisease name# pubmedsSource
TgeneFASLGC0878544Cardiomyopathies2CTD_human
TgeneFASLGC0003873Rheumatoid Arthritis1CTD_human
TgeneFASLGC0004153Atherosclerosis1CTD_human
TgeneFASLGC0007131Non-Small Cell Lung Carcinoma1CTD_human
TgeneFASLGC0007193Cardiomyopathy, Dilated1CTD_human
TgeneFASLGC0007273Carotid Artery Diseases1CTD_human
TgeneFASLGC0011875Diabetic Angiopathies1CTD_human
TgeneFASLGC0013182Drug Allergy1CTD_human
TgeneFASLGC0019158Hepatitis1CTD_human
TgeneFASLGC0020474Hyperlipidemia, Familial Combined1CTD_human
TgeneFASLGC0025202melanoma1CTD_human
TgeneFASLGC0033578Prostatic Neoplasms1CTD_human
TgeneFASLGC0039584Testicular Diseases1CTD_human
TgeneFASLGC0162557Liver Failure, Acute1CTD_human
TgeneFASLGC0242488Acute Lung Injury1CTD_human
TgeneFASLGC1328840Autoimmune Lymphoproliferative Syndrome1ORPHANET;UNIPROT