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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: 27461

FusionGeneSummary for PLAT_SUPT16H

check button Fusion gene summary
Fusion gene informationFusion gene name: PLAT_SUPT16H
Fusion gene ID: 27461
HgeneTgene
Gene symbol

PLAT

SUPT16H

Gene ID

5327

11198

Gene nameplasminogen activator, tissue typeSPT16 homolog, facilitates chromatin remodeling subunit
SynonymsT-PA|TPACDC68|FACTP140|SPT16|SPT16/CDC68
Cytomap

8p11.21

14q11.2

Type of geneprotein-codingprotein-coding
Descriptiontissue-type plasminogen activatoralteplaseplasminogen/activator kringlereteplaset-plasminogen activatorFACT complex subunit SPT16FACT 140 kDa subunitchromatin-specific transcription elongation factor 140 kDa subunitfacilitates chromatin remodeling 140 kDa subunitfacilitates chromatin transcription complex subunit SPT16hSPT16suppressor of Ty 16 homolo
Modification date2018052320180523
UniProtAcc

P00750

Q9Y5B9

Ensembl transtripts involved in fusion geneENST00000270189, ENST00000429089, 
ENST00000220809, ENST00000352041, 
ENST00000519510, ENST00000429710, 
ENST00000524009, 
ENST00000216297, 
ENST00000555943, 
Fusion gene scores* DoF score3 X 2 X 2=1237 X 4 X 15=2220
# samples 440
** MAII scorelog2(4/12*10)=1.73696559416621
effective Gene in Pan-Cancer Fusion Genes (eGinPCFGs).
DoF>8 and MAII>0
log2(40/2220*10)=-2.47248777146274
possibly effective Gene in Pan-Cancer Fusion Genes (peGinPCFGs).
DoF>8 and MAII<0
Context

PubMed: PLAT [Title/Abstract] AND SUPT16H [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
HgenePLAT

GO:0031639

plasminogen activation

12694198|17849409|24196407

HgenePLAT

GO:0045861

negative regulation of proteolysis

1695900


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
TCGARVHNSCTCGA-DQ-7589-01APLATchr8

42032755

-SUPT16Hchr14

21829491

-
* 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
intron-intronENST00000270189ENST00000216297PLATchr8

42032755

-SUPT16Hchr14

21829491

-
intron-intronENST00000270189ENST00000555943PLATchr8

42032755

-SUPT16Hchr14

21829491

-
5CDS-intronENST00000429089ENST00000216297PLATchr8

42032755

-SUPT16Hchr14

21829491

-
5CDS-intronENST00000429089ENST00000555943PLATchr8

42032755

-SUPT16Hchr14

21829491

-
5CDS-intronENST00000220809ENST00000216297PLATchr8

42032755

-SUPT16Hchr14

21829491

-
5CDS-intronENST00000220809ENST00000555943PLATchr8

42032755

-SUPT16Hchr14

21829491

-
5CDS-intronENST00000352041ENST00000216297PLATchr8

42032755

-SUPT16Hchr14

21829491

-
5CDS-intronENST00000352041ENST00000555943PLATchr8

42032755

-SUPT16Hchr14

21829491

-
intron-intronENST00000519510ENST00000216297PLATchr8

42032755

-SUPT16Hchr14

21829491

-
intron-intronENST00000519510ENST00000555943PLATchr8

42032755

-SUPT16Hchr14

21829491

-
intron-intronENST00000429710ENST00000216297PLATchr8

42032755

-SUPT16Hchr14

21829491

-
intron-intronENST00000429710ENST00000555943PLATchr8

42032755

-SUPT16Hchr14

21829491

-
intron-intronENST00000524009ENST00000216297PLATchr8

42032755

-SUPT16Hchr14

21829491

-
intron-intronENST00000524009ENST00000555943PLATchr8

42032755

-SUPT16Hchr14

21829491

-

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FusionProtFeatures for PLAT_SUPT16H


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

P00750

SUPT16H

Q9Y5B9

Component of the FACT complex, a general chromatinfactor that acts to reorganize nucleosomes. The FACT complex isinvolved in multiple processes that require DNA as a template suchas mRNA elongation, DNA replication and DNA repair. Duringtranscription elongation the FACT complex acts as a histonechaperone that both destabilizes and restores nucleosomalstructure. It facilitates the passage of RNA polymerase II andtranscription by promoting the dissociation of one histone H2A-H2Bdimer from the nucleosome, then subsequently promotes thereestablishment of the nucleosome following the passage of RNApolymerase II. The FACT complex is probably also involved inphosphorylation of 'Ser-392' of p53/TP53 via its association withCK2 (casein kinase II). {ECO:0000269|PubMed:10912001,ECO:0000269|PubMed:11239457, ECO:0000269|PubMed:12934006,ECO:0000269|PubMed:16713563, ECO:0000269|PubMed:9489704,ECO:0000269|PubMed:9836642}.

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 PLAT_SUPT16H


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 PLAT_SUPT16H


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
PLATCLEC3B, CALR, PLAU, KRT8, ANXA2, SERPINI1, SERPINA5, F2, SERPINE1, FGA, LRP1, HMGB1, F10, FN1, LAMA1, TERF2, POT1, PDGFC, FGL1, DCN, TMEM25, PTPRK, IFNA14, LAMA3, SERPINB2, SERPING1, SERPINA10, PLA2G10, SERPINB6, SERPINE2, IGFBP1, DEFA1SUPT16HBRCC3, PRKAA1, POLR1A, POLR1E, SSRP1, CHD1L, MCM4, PAF1, PARP1, H2AFX, MKL1, H3F3A, TRIM33, TAL1, CDK9, SUPT16H, MMS22L, TONSL, SMARCAD1, SREK1, SOX2, HDGF, ELAVL1, XRCC5, CUL3, CDK2, CAND1, FYTTD1, CSNK2A1, CSNK2B, SAP18, RTF1, LEO1, TOP1, DHX15, CTR9, IK, PRPF4B, SNRPD2, NCSTN, S100A9, HNRNPM, NHP2L1, DDX21, PRPF6, SF3A1, SNRPD1, PRPF3, ACIN1, EEF1A1, RBM25, MSH6, PRPF8, USP39, MSH2, PSIP1, CENPA, ESR1, FMNL1, VCP, PNKP, CD81, IGSF8, ICAM1, SRPK2, FTH1, QRICH1, RNF20, ATRX, HIST1H2AB, MOV10, NXF1, BRCA1, CUL7, OBSL1, EED, RNF2, BMI1, SUMO2, ABCE1, RPA4, SPIN2B, RPA2, SPIN1, TIPIN, RNF146, POLB, APLF, HIST1H2BA, MAFF, FBXW11, BRD3, CDK12, HMGB1, IWS1, NAP1L1, PES1, SRRM1, CDK11A, HMGB2, HMGB3, KRI1, TOP2B, ZC3H18, SFN, NTRK1, IFI16, MED4, EWSR1, CEP97, CNTROB, SPICE1, CEP164, DCTN1, POC1B, STIL, HIST1H3E, DAXX, HNRNPU, NPM1, RPL10, ETAA1, CENPQ, NF2, NANOG, UBR5, SBF1, HIST1H3A, MACROD1, H2AFY2, XPC, XRCC6, HIST1H4A, NAA40, WDR76, ALX3, TEAD2, L3MBTL1, CETN1, SIX2, POLL, RPA3, WRN, COX15, DLD, PDHA1, VDAC1, TRIM25, YAP1, MTF1


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 PLAT_SUPT16H


check button Drugs targeting genes involved in this fusion gene.
(DrugBank Version 5.1.0 2018-04-02)
PartnerGeneUniProtAccDrugBank IDDrug nameDrug activityDrug typeDrug status
HgenePLATP00750DB01050IbuprofenTissue-type plasminogen activatorsmall moleculeapproved
HgenePLATP00750DB06404Human C1-esterase inhibitorTissue-type plasminogen activatorbiotechapproved
HgenePLATP00750DB00513Aminocaproic AcidTissue-type plasminogen activatorsmall moleculeapproved|investigational
HgenePLATP00750DB01088IloprostTissue-type plasminogen activatorsmall moleculeapproved|investigational
HgenePLATP00750DB09213DexibuprofenTissue-type plasminogen activatorsmall moleculeapproved|investigational
HgenePLATP00750DB09228Conestat alfaTissue-type plasminogen activatorbiotechapproved|investigational
HgenePLATP00750DB00013UrokinaseTissue-type plasminogen activatorbiotechapproved|investigational|withdrawn

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RelatedDiseases for PLAT_SUPT16H


check button Diseases associated with fusion partners.
(DisGeNet 4.0)
PartnerGeneDisease IDDisease name# pubmedsSource
HgenePLATC0038454Cerebrovascular accident59CTD_human
HgenePLATC0027051Myocardial Infarction35CTD_human
HgenePLATC0007786Brain Ischemia25CTD_human
HgenePLATC2937358Cerebral Hemorrhage21CTD_human
HgenePLATC0151699Intracranial Hemorrhages14CTD_human
HgenePLATC0034065Pulmonary Embolism9CTD_human
HgenePLATC0019080Hemorrhage8CTD_human
HgenePLATC0007785Cerebral Infarction6CTD_human
HgenePLATC0040053Thrombosis4CTD_human
HgenePLATC0740392Infarction, Middle Cerebral Artery4CTD_human
HgenePLATC0002994Angioedema3CTD_human
HgenePLATC0010072Coronary Thrombosis3CTD_human
HgenePLATC0042487Venous Thrombosis3CTD_human
HgenePLATC0007781Intracranial Embolism and Thrombosis2CTD_human
HgenePLATC0877172Hematoma, Epidural, Spinal2CTD_human
HgenePLATC0001125Acidosis, Lactic1CTD_human
HgenePLATC0001883Airway Obstruction1CTD_human
HgenePLATC0003537Aphasia1CTD_human
HgenePLATC0003838Arterial Occlusive Diseases1CTD_human
HgenePLATC0004153Atherosclerosis1CTD_human
HgenePLATC0004604Back Pain1CTD_human
HgenePLATC0004610Bacteremia1CTD_human
HgenePLATC0007177Cardiac Tamponade1CTD_human
HgenePLATC0013922Embolism1CTD_human
HgenePLATC0018801Heart failure1CTD_human
HgenePLATC0018946Hematoma, Subdural1CTD_human
HgenePLATC0020538Hypertensive disease1CTD_human
HgenePLATC0020649Hypotension1CTD_human
HgenePLATC0023893Liver Cirrhosis, Experimental1CTD_human
HgenePLATC0024031Low Back Pain1CTD_human
HgenePLATC0025309Meningoencephalitis1CTD_human
HgenePLATC0027746Nerve Degeneration1CTD_human
HgenePLATC0030552Paresis1CTD_human
HgenePLATC0031039Pericardial effusion1CTD_human
HgenePLATC0033975Psychotic Disorders1PSYGENET
HgenePLATC0035126Reperfusion Injury1CTD_human
HgenePLATC0035229Respiratory Insufficiency1CTD_human
HgenePLATC0036341Schizophrenia1PSYGENET
HgenePLATC0036980Shock, Cardiogenic1CTD_human
HgenePLATC0037926Compression of spinal cord1CTD_human
HgenePLATC0040038Thromboembolism1CTD_human
HgenePLATC0085307Embolism and Thrombosis1CTD_human
HgenePLATC0149649Cholesterol Embolism1CTD_human
HgenePLATC0162820Dermatitis, Allergic Contact1CTD_human
HgenePLATC0235032Neurotoxicity Syndromes1CTD_human
HgenePLATC0236733Amphetamine-Related Disorders1CTD_human
HgenePLATC0242184Hypoxia1CTD_human
HgenePLATC0242698Ventricular Dysfunction, Left1CTD_human
HgenePLATC0349204Nonorganic psychosis1PSYGENET
HgenePLATC0740858Substance abuse problem1PSYGENET
HgenePLATC0751895Vasospasm, Intracranial1CTD_human
HgenePLATC0751955Brain Infarction1CTD_human
HgenePLATC0752143Intracranial Thrombosis1CTD_human
HgenePLATC1861172Venous Thromboembolism1CTD_human
HgenePLATC4277682Chemical and Drug Induced Liver Injury1CTD_human