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Center for Computational Systems Medicine level1
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Fusion Gene Summary

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Fusion Gene Sample Information

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Fusion ORF Analysis

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Fusion Amino Acid Sequences

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Fusion Protein Functional Features

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Fusion Protein-Protein Interaction

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Related drugs with this fusion protein

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Related disease with this fusion protein

Fusion Protein:PVR-SIRT2

Fusion Protein Summary

check button Fusion gene summary
Fusion partner gene informationFusion gene name: PVR-SIRT2
FusionPDB ID: 70766
FusionGDB2.0 ID: 70766
HgeneTgene
Gene symbol

PVR

SIRT2

Gene ID

5817

22933

Gene namePVR cell adhesion moleculesirtuin 2
SynonymsCD155|HVED|NECL5|Necl-5|PVS|TAGE4SIR2|SIR2L|SIR2L2
Cytomap

19q13.31

19q13.2

Type of geneprotein-codingprotein-coding
Descriptionpoliovirus receptornectin-like protein 5NAD-dependent protein deacetylase sirtuin-2NAD-dependent deacetylase sirtuin-2SIR2-like protein 2regulatory protein SIR2 homolog 2silent information regulator 2sir2-related protein type 2sirtuin type 2
Modification date2020032920200329
UniProtAcc..
Ensembl transtripts involved in fusion geneENST idsENST00000344956, ENST00000403059, 
ENST00000406449, ENST00000425690, 
ENST00000481381, ENST00000249396, 
ENST00000358931, ENST00000392081, 
Fusion gene scores for assessment (based on all fusion genes of FusionGDB 2.0)* DoF score5 X 7 X 5=1756 X 6 X 6=216
# samples 67
** MAII scorelog2(6/175*10)=-1.54432051622381
possibly effective Gene in Pan-Cancer Fusion Genes (peGinPCFGs).
DoF>8 and MAII<0
log2(7/216*10)=-1.6256044852185
possibly effective Gene in Pan-Cancer Fusion Genes (peGinPCFGs).
DoF>8 and MAII<0
Context (manual curation of fusion genes in FusionPDB)

PubMed: PVR [Title/Abstract] AND SIRT2 [Title/Abstract] AND fusion [Title/Abstract]

Most frequent breakpoint (based on all fusion genes of FusionGDB 2.0)PVR(45147475)-SIRT2(39372131), # samples:2
Anticipated loss of major functional domain due to fusion event.PVR-SIRT2 seems lost the major protein functional domain in Hgene partner, which is a CGC by not retaining the major functional domain in the partially deleted in-frame ORF.
PVR-SIRT2 seems lost the major protein functional domain in Hgene partner, which is a CGC by not retaining the major functional domain in the partially deleted in-frame ORF.
PVR-SIRT2 seems lost the major protein functional domain in Hgene partner, which is a essential gene by not retaining the major functional domain in the partially deleted in-frame ORF.
PVR-SIRT2 seems lost the major protein functional domain in Hgene partner, which is a essential gene by not retaining the major functional domain in the partially deleted in-frame ORF.
* 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
HgenePVR

GO:0060370

susceptibility to T cell mediated cytotoxicity

15039383

TgeneSIRT2

GO:0000122

negative regulation of transcription by RNA polymerase II

18722353

TgeneSIRT2

GO:0006471

protein ADP-ribosylation

10381378

TgeneSIRT2

GO:0006476

protein deacetylation

17172643|20543840|21949390

TgeneSIRT2

GO:0034983

peptidyl-lysine deacetylation

23932781

TgeneSIRT2

GO:0035729

cellular response to hepatocyte growth factor stimulus

23908241

TgeneSIRT2

GO:0045843

negative regulation of striated muscle tissue development

12887892

TgeneSIRT2

GO:0045892

negative regulation of transcription, DNA-templated

12887892

TgeneSIRT2

GO:0048012

hepatocyte growth factor receptor signaling pathway

23908241

TgeneSIRT2

GO:0070933

histone H4 deacetylation

16648462|17488717

TgeneSIRT2

GO:0071219

cellular response to molecule of bacterial origin

23908241

TgeneSIRT2

GO:0071456

cellular response to hypoxia

24681946

TgeneSIRT2

GO:0090042

tubulin deacetylation

18722353|23886946


check buttonFusion gene breakpoints across PVR (5'-gene)
* Click on the image to open the UCSC genome browser with custom track showing this image in a new window.
all structure

check buttonFusion gene breakpoints across SIRT2 (3'-gene)
* Click on the image to open the UCSC genome browser with custom track showing this image in a new window.
all structure


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Fusion Gene Sample Information

check buttonFusion gene information from FusionGDB2.0.
check button Fusion gene information from two resources (ChiTars 5.0 and ChimerDB 4.0)
* 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.
SourceDiseaseSampleHgeneHchrHbpHstrandTgeneTchrTbpTstrand
ChimerDB4UCSTCGA-N7-A4Y8-01APVRchr19

45147475

-SIRT2chr19

39372131

-
ChimerDB4UCSTCGA-N7-A4Y8-01APVRchr19

45147475

+SIRT2chr19

39372131

-


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Fusion ORF Analysis


check buttonFusion information from ORFfinder translation from full-length transcript sequence from FusionPDB.
HenstTenstHgeneHchrHbpHstrandTgeneTchrTbpTstrandSeq length
(transcript)
BP loci
(transcript)
Predicted start
(transcript)
Predicted stop
(transcript)
Seq length
(amino acids)
ENST00000425690PVRchr1945147475+ENST00000249396SIRT2chr1939372131-1515378122916264
ENST00000425690PVRchr1945147475+ENST00000392081SIRT2chr1939372131-1515378122916264
ENST00000425690PVRchr1945147475+ENST00000358931SIRT2chr1939372131-1339378122562146
ENST00000344956PVRchr1945147475+ENST00000249396SIRT2chr1939372131-1515378122916264
ENST00000344956PVRchr1945147475+ENST00000392081SIRT2chr1939372131-1515378122916264
ENST00000344956PVRchr1945147475+ENST00000358931SIRT2chr1939372131-1339378122562146
ENST00000403059PVRchr1945147475+ENST00000249396SIRT2chr1939372131-140326610804264
ENST00000403059PVRchr1945147475+ENST00000392081SIRT2chr1939372131-140326610804264
ENST00000403059PVRchr1945147475+ENST00000358931SIRT2chr1939372131-122726610450146
ENST00000406449PVRchr1945147475+ENST00000249396SIRT2chr1939372131-1216790617205
ENST00000406449PVRchr1945147475+ENST00000392081SIRT2chr1939372131-1216790617205
ENST00000406449PVRchr1945147475+ENST00000358931SIRT2chr1939372131-104079547119142

check buttonDeepORF prediction of the coding potential based on the fusion transcript sequence of in-frame fusion genes. DeepORF is a coding potential classifier based on convolutional neural network by comparing the real Ribo-seq data. If the no-coding score < 0.5 and coding score > 0.5, then the in-frame fusion transcript is predicted as being likely translated.
HenstTenstHgeneHchrHbpHstrandTgeneTchrTbpTstrandNo-coding scoreCoding score
ENST00000425690ENST00000249396PVRchr1945147475+SIRT2chr1939372131-0.0410342370.9589658
ENST00000425690ENST00000392081PVRchr1945147475+SIRT2chr1939372131-0.0410342370.9589658
ENST00000425690ENST00000358931PVRchr1945147475+SIRT2chr1939372131-0.95189470.048105367
ENST00000344956ENST00000249396PVRchr1945147475+SIRT2chr1939372131-0.0410342370.9589658
ENST00000344956ENST00000392081PVRchr1945147475+SIRT2chr1939372131-0.0410342370.9589658
ENST00000344956ENST00000358931PVRchr1945147475+SIRT2chr1939372131-0.95189470.048105367
ENST00000403059ENST00000249396PVRchr1945147475+SIRT2chr1939372131-0.0501719680.9498281
ENST00000403059ENST00000392081PVRchr1945147475+SIRT2chr1939372131-0.0501719680.9498281
ENST00000403059ENST00000358931PVRchr1945147475+SIRT2chr1939372131-0.96344270.036557317
ENST00000406449ENST00000249396PVRchr1945147475+SIRT2chr1939372131-0.043729250.95627075
ENST00000406449ENST00000392081PVRchr1945147475+SIRT2chr1939372131-0.043729250.95627075
ENST00000406449ENST00000358931PVRchr1945147475+SIRT2chr1939372131-0.969006060.03099397

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Fusion Amino Acid Sequences


check button For individual full-length fusion transcript sequence from FusionPDB, we ran ORFfinder and chose the longest ORF among the all predicted ones.
>FusionGDB ID_FusionGDB isoform ID_FGname_Hgene_Hchr_Hbp_Henst_Tgene_Tchr_Tbp_Tenst_length(fusion AA) seq_BP

>70766_70766_1_PVR-SIRT2_PVR_chr19_45147475_ENST00000344956_SIRT2_chr19_39372131_ENST00000249396_length(amino acids)=264AA_BP=77
MELEEVGIPLPTPGTGGAAPRGFQDLSSGSWTRSDRGRASGRREARRRPREAQLLGATGMARAMAAAWPLLLVALLVLSWPPPGTEKIFS
EVTPKCEDCQSLVKPDIVFFGESLPARFFSCMQSDFLKVDLLLVMGTSLQVQPFASLISKAPLSTPRLLINKEKAGQSDPFLGMIMGLGG

--------------------------------------------------------------

>70766_70766_2_PVR-SIRT2_PVR_chr19_45147475_ENST00000344956_SIRT2_chr19_39372131_ENST00000358931_length(amino acids)=146AA_BP=77
MELEEVGIPLPTPGTGGAAPRGFQDLSSGSWTRSDRGRASGRREARRRPREAQLLGATGMARAMAAAWPLLLVALLVLSWPPPGTEKIFS

--------------------------------------------------------------

>70766_70766_3_PVR-SIRT2_PVR_chr19_45147475_ENST00000344956_SIRT2_chr19_39372131_ENST00000392081_length(amino acids)=264AA_BP=77
MELEEVGIPLPTPGTGGAAPRGFQDLSSGSWTRSDRGRASGRREARRRPREAQLLGATGMARAMAAAWPLLLVALLVLSWPPPGTEKIFS
EVTPKCEDCQSLVKPDIVFFGESLPARFFSCMQSDFLKVDLLLVMGTSLQVQPFASLISKAPLSTPRLLINKEKAGQSDPFLGMIMGLGG

--------------------------------------------------------------

>70766_70766_4_PVR-SIRT2_PVR_chr19_45147475_ENST00000403059_SIRT2_chr19_39372131_ENST00000249396_length(amino acids)=264AA_BP=77
MELEEVGIPLPTPGTGGAAPRGFQDLSSGSWTRSDRGRASGRREARRRPREAQLLGATGMARAMAAAWPLLLVALLVLSWPPPGTEKIFS
EVTPKCEDCQSLVKPDIVFFGESLPARFFSCMQSDFLKVDLLLVMGTSLQVQPFASLISKAPLSTPRLLINKEKAGQSDPFLGMIMGLGG

--------------------------------------------------------------

>70766_70766_5_PVR-SIRT2_PVR_chr19_45147475_ENST00000403059_SIRT2_chr19_39372131_ENST00000358931_length(amino acids)=146AA_BP=77
MELEEVGIPLPTPGTGGAAPRGFQDLSSGSWTRSDRGRASGRREARRRPREAQLLGATGMARAMAAAWPLLLVALLVLSWPPPGTEKIFS

--------------------------------------------------------------

>70766_70766_6_PVR-SIRT2_PVR_chr19_45147475_ENST00000403059_SIRT2_chr19_39372131_ENST00000392081_length(amino acids)=264AA_BP=77
MELEEVGIPLPTPGTGGAAPRGFQDLSSGSWTRSDRGRASGRREARRRPREAQLLGATGMARAMAAAWPLLLVALLVLSWPPPGTEKIFS
EVTPKCEDCQSLVKPDIVFFGESLPARFFSCMQSDFLKVDLLLVMGTSLQVQPFASLISKAPLSTPRLLINKEKAGQSDPFLGMIMGLGG

--------------------------------------------------------------

>70766_70766_7_PVR-SIRT2_PVR_chr19_45147475_ENST00000406449_SIRT2_chr19_39372131_ENST00000249396_length(amino acids)=205AA_BP=18
MARAMAAAWPLLLVALLVLSWPPPGTEKIFSEVTPKCEDCQSLVKPDIVFFGESLPARFFSCMQSDFLKVDLLLVMGTSLQVQPFASLIS
KAPLSTPRLLINKEKAGQSDPFLGMIMGLGGGMDFDSKKAYRDVAWLGECDQGCLALAELLGWKKELEDLVRREHASIDAQSGAGVPNPS

--------------------------------------------------------------

>70766_70766_8_PVR-SIRT2_PVR_chr19_45147475_ENST00000406449_SIRT2_chr19_39372131_ENST00000358931_length(amino acids)=142AA_BP=
MLVKRGPGPVGAQLSLRSSASRLGDAAVTGVSPSLLSWPRPWQVAGTSWGKLKCWGWGPPPPTGHLCWRAPSGQGPPAPSSIQGAQQGPG

--------------------------------------------------------------

>70766_70766_9_PVR-SIRT2_PVR_chr19_45147475_ENST00000406449_SIRT2_chr19_39372131_ENST00000392081_length(amino acids)=205AA_BP=18
MARAMAAAWPLLLVALLVLSWPPPGTEKIFSEVTPKCEDCQSLVKPDIVFFGESLPARFFSCMQSDFLKVDLLLVMGTSLQVQPFASLIS
KAPLSTPRLLINKEKAGQSDPFLGMIMGLGGGMDFDSKKAYRDVAWLGECDQGCLALAELLGWKKELEDLVRREHASIDAQSGAGVPNPS

--------------------------------------------------------------

>70766_70766_10_PVR-SIRT2_PVR_chr19_45147475_ENST00000425690_SIRT2_chr19_39372131_ENST00000249396_length(amino acids)=264AA_BP=77
MELEEVGIPLPTPGTGGAAPRGFQDLSSGSWTRSDRGRASGRREARRRPREAQLLGATGMARAMAAAWPLLLVALLVLSWPPPGTEKIFS
EVTPKCEDCQSLVKPDIVFFGESLPARFFSCMQSDFLKVDLLLVMGTSLQVQPFASLISKAPLSTPRLLINKEKAGQSDPFLGMIMGLGG

--------------------------------------------------------------

>70766_70766_11_PVR-SIRT2_PVR_chr19_45147475_ENST00000425690_SIRT2_chr19_39372131_ENST00000358931_length(amino acids)=146AA_BP=77
MELEEVGIPLPTPGTGGAAPRGFQDLSSGSWTRSDRGRASGRREARRRPREAQLLGATGMARAMAAAWPLLLVALLVLSWPPPGTEKIFS

--------------------------------------------------------------

>70766_70766_12_PVR-SIRT2_PVR_chr19_45147475_ENST00000425690_SIRT2_chr19_39372131_ENST00000392081_length(amino acids)=264AA_BP=77
MELEEVGIPLPTPGTGGAAPRGFQDLSSGSWTRSDRGRASGRREARRRPREAQLLGATGMARAMAAAWPLLLVALLVLSWPPPGTEKIFS
EVTPKCEDCQSLVKPDIVFFGESLPARFFSCMQSDFLKVDLLLVMGTSLQVQPFASLISKAPLSTPRLLINKEKAGQSDPFLGMIMGLGG

--------------------------------------------------------------

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Fusion Protein Functional Features


check button Four levels of functional features of fusion genes
Go to FGviewer search page for the most frequent breakpoint (https://ccsmweb.uth.edu/FGviewer/chr19:45147475/chr19:39372131)
- FGviewer provides the online visualization of the retention search of the protein functional features across DNA, RNA, protein, and pathological levels.
- How to search
1. Put your fusion gene symbol.
2. Press the tab key until there will be shown the breakpoint information filled.
4. Go down and press 'Search' tab twice.
4. Go down to have the hyperlink of the search result.
5. Click the hyperlink.
6. See the FGviewer result for your fusion gene.
FGviewer

check buttonMain function of each fusion partner protein. (from UniProt)
HgeneTgene
..
FUNCTION: Might normally function as a transcriptional repressor. EWS-fusion-proteins (EFPS) may play a role in the tumorigenic process. They may disturb gene expression by mimicking, or interfering with the normal function of CTD-POLII within the transcription initiation complex. They may also contribute to an aberrant activation of the fusion protein target genes.FUNCTION: Might normally function as a transcriptional repressor. EWS-fusion-proteins (EFPS) may play a role in the tumorigenic process. They may disturb gene expression by mimicking, or interfering with the normal function of CTD-POLII within the transcription initiation complex. They may also contribute to an aberrant activation of the fusion protein target genes.

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.
- Retained protein feature among the 13 regional features.
PartnerGeneHbpTbpENSTStrandBPexonTotalExonProtein feature loci*BPlociTotalLenProtein featureProtein feature note
TgeneSIRT2chr19:45147475chr19:39372131ENST00000249396816262_263210.33333333333334390.0Nucleotide bindingNAD
TgeneSIRT2chr19:45147475chr19:39372131ENST00000249396816286_288210.33333333333334390.0Nucleotide bindingNAD
TgeneSIRT2chr19:45147475chr19:39372131ENST00000358931814262_263210.33333333333334452.6666666666667Nucleotide bindingNAD
TgeneSIRT2chr19:45147475chr19:39372131ENST00000358931814286_288210.33333333333334452.6666666666667Nucleotide bindingNAD
TgeneSIRT2chr19:45147475chr19:39372131ENST00000392081715262_263173.33333333333334353.0Nucleotide bindingNAD
TgeneSIRT2chr19:45147475chr19:39372131ENST00000392081715286_288173.33333333333334353.0Nucleotide bindingNAD
TgeneSIRT2chr19:45147475chr19:39372131ENST00000249396816232_301210.33333333333334390.0RegionNote=Peptide inhibitor binding
TgeneSIRT2chr19:45147475chr19:39372131ENST00000358931814232_301210.33333333333334452.6666666666667RegionNote=Peptide inhibitor binding
TgeneSIRT2chr19:45147475chr19:39372131ENST00000392081715232_301173.33333333333334353.0RegionNote=Peptide inhibitor binding

- Not-retained protein feature among the 13 regional features.
PartnerGeneHbpTbpENSTStrandBPexonTotalExonProtein feature loci*BPlociTotalLenProtein featureProtein feature note
HgenePVRchr19:45147475chr19:39372131ENST00000344956+17145_23726.333333333333332365.0DomainNote=Ig-like C2-type 1
HgenePVRchr19:45147475chr19:39372131ENST00000344956+17244_32826.333333333333332365.0DomainNote=Ig-like C2-type 2
HgenePVRchr19:45147475chr19:39372131ENST00000344956+1724_13926.333333333333332365.0DomainNote=Ig-like V-type
HgenePVRchr19:45147475chr19:39372131ENST00000403059+18145_23726.333333333333332373.0DomainNote=Ig-like C2-type 1
HgenePVRchr19:45147475chr19:39372131ENST00000403059+18244_32826.333333333333332373.0DomainNote=Ig-like C2-type 2
HgenePVRchr19:45147475chr19:39372131ENST00000403059+1824_13926.333333333333332373.0DomainNote=Ig-like V-type
HgenePVRchr19:45147475chr19:39372131ENST00000406449+16145_23726.333333333333332393.0DomainNote=Ig-like C2-type 1
HgenePVRchr19:45147475chr19:39372131ENST00000406449+16244_32826.333333333333332393.0DomainNote=Ig-like C2-type 2
HgenePVRchr19:45147475chr19:39372131ENST00000406449+1624_13926.333333333333332393.0DomainNote=Ig-like V-type
HgenePVRchr19:45147475chr19:39372131ENST00000425690+18145_23726.333333333333332418.0DomainNote=Ig-like C2-type 1
HgenePVRchr19:45147475chr19:39372131ENST00000425690+18244_32826.333333333333332418.0DomainNote=Ig-like C2-type 2
HgenePVRchr19:45147475chr19:39372131ENST00000425690+1824_13926.333333333333332418.0DomainNote=Ig-like V-type
HgenePVRchr19:45147475chr19:39372131ENST00000344956+17396_40126.333333333333332365.0MotifNote=ITIM motif
HgenePVRchr19:45147475chr19:39372131ENST00000403059+18396_40126.333333333333332373.0MotifNote=ITIM motif
HgenePVRchr19:45147475chr19:39372131ENST00000406449+16396_40126.333333333333332393.0MotifNote=ITIM motif
HgenePVRchr19:45147475chr19:39372131ENST00000425690+18396_40126.333333333333332418.0MotifNote=ITIM motif
HgenePVRchr19:45147475chr19:39372131ENST00000344956+17368_37226.333333333333332365.0RegionNote=DYNLT1 binding
HgenePVRchr19:45147475chr19:39372131ENST00000403059+18368_37226.333333333333332373.0RegionNote=DYNLT1 binding
HgenePVRchr19:45147475chr19:39372131ENST00000406449+16368_37226.333333333333332393.0RegionNote=DYNLT1 binding
HgenePVRchr19:45147475chr19:39372131ENST00000425690+18368_37226.333333333333332418.0RegionNote=DYNLT1 binding
HgenePVRchr19:45147475chr19:39372131ENST00000344956+1721_34326.333333333333332365.0Topological domainExtracellular
HgenePVRchr19:45147475chr19:39372131ENST00000344956+17368_41726.333333333333332365.0Topological domainCytoplasmic
HgenePVRchr19:45147475chr19:39372131ENST00000403059+1821_34326.333333333333332373.0Topological domainExtracellular
HgenePVRchr19:45147475chr19:39372131ENST00000403059+18368_41726.333333333333332373.0Topological domainCytoplasmic
HgenePVRchr19:45147475chr19:39372131ENST00000406449+1621_34326.333333333333332393.0Topological domainExtracellular
HgenePVRchr19:45147475chr19:39372131ENST00000406449+16368_41726.333333333333332393.0Topological domainCytoplasmic
HgenePVRchr19:45147475chr19:39372131ENST00000425690+1821_34326.333333333333332418.0Topological domainExtracellular
HgenePVRchr19:45147475chr19:39372131ENST00000425690+18368_41726.333333333333332418.0Topological domainCytoplasmic
HgenePVRchr19:45147475chr19:39372131ENST00000344956+17344_36726.333333333333332365.0TransmembraneHelical
HgenePVRchr19:45147475chr19:39372131ENST00000403059+18344_36726.333333333333332373.0TransmembraneHelical
HgenePVRchr19:45147475chr19:39372131ENST00000406449+16344_36726.333333333333332393.0TransmembraneHelical
HgenePVRchr19:45147475chr19:39372131ENST00000425690+18344_36726.333333333333332418.0TransmembraneHelical
TgeneSIRT2chr19:45147475chr19:39372131ENST0000024939681665_340210.33333333333334390.0DomainDeacetylase sirtuin-type
TgeneSIRT2chr19:45147475chr19:39372131ENST0000035893181465_340210.33333333333334452.6666666666667DomainDeacetylase sirtuin-type
TgeneSIRT2chr19:45147475chr19:39372131ENST0000039208171565_340173.33333333333334353.0DomainDeacetylase sirtuin-type
TgeneSIRT2chr19:45147475chr19:39372131ENST0000024939681641_51210.33333333333334390.0MotifNote=Nuclear export signal
TgeneSIRT2chr19:45147475chr19:39372131ENST0000035893181441_51210.33333333333334452.6666666666667MotifNote=Nuclear export signal
TgeneSIRT2chr19:45147475chr19:39372131ENST0000039208171541_51173.33333333333334353.0MotifNote=Nuclear export signal
TgeneSIRT2chr19:45147475chr19:39372131ENST00000249396816167_170210.33333333333334390.0Nucleotide bindingNAD
TgeneSIRT2chr19:45147475chr19:39372131ENST0000024939681685_89210.33333333333334390.0Nucleotide bindingNAD
TgeneSIRT2chr19:45147475chr19:39372131ENST0000024939681695_97210.33333333333334390.0Nucleotide bindingNAD
TgeneSIRT2chr19:45147475chr19:39372131ENST00000358931814167_170210.33333333333334452.6666666666667Nucleotide bindingNAD
TgeneSIRT2chr19:45147475chr19:39372131ENST0000035893181485_89210.33333333333334452.6666666666667Nucleotide bindingNAD
TgeneSIRT2chr19:45147475chr19:39372131ENST0000035893181495_97210.33333333333334452.6666666666667Nucleotide bindingNAD
TgeneSIRT2chr19:45147475chr19:39372131ENST00000392081715167_170173.33333333333334353.0Nucleotide bindingNAD
TgeneSIRT2chr19:45147475chr19:39372131ENST0000039208171585_89173.33333333333334353.0Nucleotide bindingNAD
TgeneSIRT2chr19:45147475chr19:39372131ENST0000039208171595_97173.33333333333334353.0Nucleotide bindingNAD
TgeneSIRT2chr19:45147475chr19:39372131ENST00000249396816116_120210.33333333333334390.0RegionNote=Peptide inhibitor binding
TgeneSIRT2chr19:45147475chr19:39372131ENST00000358931814116_120210.33333333333334452.6666666666667RegionNote=Peptide inhibitor binding
TgeneSIRT2chr19:45147475chr19:39372131ENST00000392081715116_120173.33333333333334353.0RegionNote=Peptide inhibitor binding


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Fusion Protein-Protein Interaction


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 from validated records (BIOGRID-3.4.160)
GenePPI interactors


check button Protein-protein interactors based on sequence similarity (STRING)
GeneSTRING network
PVR
SIRT2


check button - Retained interactions in fusion protein (protein functional feature from UniProt).
PartnerGeneHbpTbpENSTStrandBPexonTotalExonProtein feature loci*BPlociTotalLenStill interaction with


check button - Lost interactions due to fusion (protein functional feature from UniProt).
PartnerGeneHbpTbpENSTStrandBPexonTotalExonProtein feature loci*BPlociTotalLenInteraction lost with


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Related Drugs to PVR-SIRT2


check button Drugs used for this fusion-positive patient.
(Manual curation of PubMed, 04-30-2022 + MyCancerGenome)
HgeneTgeneDrugSourcePMID

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Related Diseases to PVR-SIRT2


check button Diseases that have this fusion gene.
(Manual curation of PubMed, 04-30-2022 + MyCancerGenome)
HgeneTgeneDiseaseSourcePMID

check button Diseases associated with fusion partners.
(DisGeNet 4.0)
PartnerGeneDisease IDDisease name# pubmedsSource