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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: 23020

FusionGeneSummary for MYH9_PLAT

check button Fusion gene summary
Fusion gene informationFusion gene name: MYH9_PLAT
Fusion gene ID: 23020
HgeneTgene
Gene symbol

MYH9

PLAT

Gene ID

4627

5327

Gene namemyosin heavy chain 9plasminogen activator, tissue type
SynonymsBDPLT6|DFNA17|EPSTS|FTNS|MHA|NMHC-II-A|NMMHC-IIA|NMMHCAT-PA|TPA
Cytomap

22q12.3

8p11.21

Type of geneprotein-codingprotein-coding
Descriptionmyosin-9cellular myosin heavy chain, type Amyosin, heavy chain 9, non-musclenon-muscle myosin heavy chain 9non-muscle myosin heavy chain Anon-muscle myosin heavy chain IIanon-muscle myosin heavy polypeptide 9nonmuscle myosin heavy chain II-Atissue-type plasminogen activatoralteplaseplasminogen/activator kringlereteplaset-plasminogen activator
Modification date2018052220180523
UniProtAcc

P35579

P00750

Ensembl transtripts involved in fusion geneENST00000216181, ENST00000475726, 
ENST00000401701, 
ENST00000270189, 
ENST00000429089, ENST00000220809, 
ENST00000352041, ENST00000519510, 
ENST00000429710, ENST00000524009, 
Fusion gene scores* DoF score36 X 33 X 15=1782027 X 5 X 11=1485
# samples 5026
** MAII scorelog2(50/17820*10)=-5.1554254317472
possibly effective Gene in Pan-Cancer Fusion Genes (peGinPCFGs).
DoF>8 and MAII<0
log2(26/1485*10)=-2.51387940265967
possibly effective Gene in Pan-Cancer Fusion Genes (peGinPCFGs).
DoF>8 and MAII<0
Context

PubMed: MYH9 [Title/Abstract] AND PLAT [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
HgeneMYH9

GO:0001525

angiogenesis

16403913

HgeneMYH9

GO:0006509

membrane protein ectodomain proteolysis

16186248

HgeneMYH9

GO:0030048

actin filament-based movement

12237319|15845534

HgeneMYH9

GO:0031032

actomyosin structure organization

24072716

TgenePLAT

GO:0031639

plasminogen activation

12694198|17849409|24196407

TgenePLAT

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
TCGARVCOADTCGA-F4-6805-01AMYH9chr22

36677327

-PLATchr8

42051245

-
* 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
5CDS-intronENST00000216181ENST00000270189MYH9chr22

36677327

-PLATchr8

42051245

-
5CDS-intronENST00000216181ENST00000429089MYH9chr22

36677327

-PLATchr8

42051245

-
5CDS-intronENST00000216181ENST00000220809MYH9chr22

36677327

-PLATchr8

42051245

-
5CDS-intronENST00000216181ENST00000352041MYH9chr22

36677327

-PLATchr8

42051245

-
5CDS-intronENST00000216181ENST00000519510MYH9chr22

36677327

-PLATchr8

42051245

-
5CDS-intronENST00000216181ENST00000429710MYH9chr22

36677327

-PLATchr8

42051245

-
5CDS-intronENST00000216181ENST00000524009MYH9chr22

36677327

-PLATchr8

42051245

-
intron-intronENST00000475726ENST00000270189MYH9chr22

36677327

-PLATchr8

42051245

-
intron-intronENST00000475726ENST00000429089MYH9chr22

36677327

-PLATchr8

42051245

-
intron-intronENST00000475726ENST00000220809MYH9chr22

36677327

-PLATchr8

42051245

-
intron-intronENST00000475726ENST00000352041MYH9chr22

36677327

-PLATchr8

42051245

-
intron-intronENST00000475726ENST00000519510MYH9chr22

36677327

-PLATchr8

42051245

-
intron-intronENST00000475726ENST00000429710MYH9chr22

36677327

-PLATchr8

42051245

-
intron-intronENST00000475726ENST00000524009MYH9chr22

36677327

-PLATchr8

42051245

-
intron-intronENST00000401701ENST00000270189MYH9chr22

36677327

-PLATchr8

42051245

-
intron-intronENST00000401701ENST00000429089MYH9chr22

36677327

-PLATchr8

42051245

-
intron-intronENST00000401701ENST00000220809MYH9chr22

36677327

-PLATchr8

42051245

-
intron-intronENST00000401701ENST00000352041MYH9chr22

36677327

-PLATchr8

42051245

-
intron-intronENST00000401701ENST00000519510MYH9chr22

36677327

-PLATchr8

42051245

-
intron-intronENST00000401701ENST00000429710MYH9chr22

36677327

-PLATchr8

42051245

-
intron-intronENST00000401701ENST00000524009MYH9chr22

36677327

-PLATchr8

42051245

-

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FusionProtFeatures for MYH9_PLAT


check buttonMain function of each fusion partner protein. (from UniProt)
HgeneTgene
MYH9

P35579

PLAT

P00750

Cellular myosin that appears to play a role incytokinesis, cell shape, and specialized functions such assecretion and capping. During cell spreading, plays an importantrole in cytoskeleton reorganization, focal contacts formation (inthe margins but not the central part of spreading cells), andlamellipodial retraction; this function is mechanicallyantagonized by MYH10. {ECO:0000269|PubMed:20052411}.

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 MYH9_PLAT


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 MYH9_PLAT


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
MYH9EPB41, MARK4, ASCC2, MYL9, PRKCE, USP1, USP45, GRB2, RAC1, YWHAZ, EMD, TERF1, TERF2, CBL, PPP2R4, AGO3, YWHAQ, MME, HDAC5, NCOA3, CREBBP, UBE3A, ARRB1, ARRB2, SIRT7, TRAF4, SP1, ISG15, FBXO25, CDK2, CUL1, TRIM72, GRK5, UBASH3B, PIK3R2, SHC1, MYL6, SPTAN1, HSP90AB1, ACTA2, MYH10, HNRNPU, FLNA, ACTR1A, RAB11A, EIF4B, SEL1L, ATP5A1, SEPT7, RALA, HSPA5, TUBA4A, EIF3A, EIF3C, TPM4, MRPS18B, PSME3, HSPA1A, ESR1, TSGA10, EIF4A3, MAGOH, TRAF3IP1, MEN1, HSP90AA1, VCAM1, FN1, IQCB1, ITGA4, PAN2, ACE, ACTB, CSNK2A1, PIK3C3, PPP2CA, CASP4, TARDBP, AKAP10, CDC73, MYH14, OTUD6B, MYL12A, RPA1, RPA2, RPA3, LGR4, IVNS1ABP, TP53, HUWE1, ALK, UBE2I, EED, AMFR, OS9, SYVN1, ATG9A, USP7, HNRNPA1, ATP5L, MYO1E, SRSF5, SSB, NTRK1, ACTA1, ACTG1, ACTN4, ACTN1, AP2A1, AP2B1, ANXA2, APOB, DST, CALD1, CALM1, CALML3, CAPZA1, CAPZA2, CAPZB, CD44, CFL1, CFL2, AP2M1, CLTA, CLTB, CLTC, CPM, DAB2, DAPK3, DBN1, DSG2, CTTN, STOM, EPS15, FLII, FLNB, FYN, GNAI1, GNAI2, GNAS, GNB2, GSN, HIP1, ITPR2, ITPR3, JUP, LGALS1, ABLIM1, LMO7, LSS, LYN, MYO1B, MSN, PDLIM7, ANLN, MYO19, MYO18A, MYLK, MYO1C, MYO5A, MYO5B, MYO6, PPP1R12A, PPP1R12B, NAP1L1, PAWR, PIK3C2A, PLEC, PLS1, PPIA, PPP1CA, PPP1CB, PPP1CC, PSMB10, TWF1, PEX5, RPL22, SIPA1, SORD, SPTBN1, SPTBN2, SSFA2, ST5, SVIL, TCEA2, TMOD1, TNFAIP1, TPM1, TPM2, TPM3, CORO2A, YES1, LUZP1, PICALM, PIP5K1A, SORBS2, IQGAP1, HIP1R, GPRC5A, LRRFIP2, CLINT1, ARHGAP11A, ARHGEF17, SEC16A, WDR1, ARPC4, ARPC3, ARPC1B, ACTR3, ACTR2, ARPC2, BCAP31, FLOT1, BASP1, IMMT, RBPMS, DSTN, TRIOBP, CEP250, AKAP2, TWF2, SYNPO, CEP162, LIMCH1, PALLD, SIPA1L3, MPRIP, COBL, KIF13B, SPECC1L, ATP13A2, MACF1, CORO1C, STX12, GCA, PLEKHG3, RAI14, ZBTB20, AHDC1, PACSIN3, TMOD3, PNMA3, FCF1, CEP83, LIMA1, GTSE1, KDM3B, UACA, CDCA8, BMP2K, UNC45A, MYO5C, GNG12, MUC13, CORO1B, MICAL3, ARHGAP21, SHROOM3, AFAP1, INF2, NARFL, METTL17, AHNAK, EFHD2, CYBRD1, WDR76, DSN1, RNF170, TRIM56, ARPC5L, ANTXR1, LZTS2, PPP1R9B, CEP89, STON2, DOCK7, DIXDC1, SSH2, NEXN, ELMSAN1, SPECC1, CCDC102A, FCHO2, MISP, JMY, CD109, ACTRT1, MYL6B, CCDC50, OARD1, GAS2L3, TTLL6, TPRN, ACTBL2, MCM2, MCM5, SNW1, CDC5L, BOP1, PES1, EGFR, CDH1, C9orf156, MYL3, H2AFY, CYLD, TRIM25, BRCA1, HDAC6PLATCLEC3B, 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, DEFA1


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 MYH9_PLAT


check button Drugs targeting genes involved in this fusion gene.
(DrugBank Version 5.1.0 2018-04-02)
PartnerGeneUniProtAccDrugBank IDDrug nameDrug activityDrug typeDrug status
HgeneMYH9P35579DB11638ArtenimolMyosin-9small moleculeapproved|investigational
TgenePLATP00750DB01050IbuprofenTissue-type plasminogen activatorsmall moleculeapproved
TgenePLATP00750DB06404Human C1-esterase inhibitorTissue-type plasminogen activatorbiotechapproved
TgenePLATP00750DB00513Aminocaproic AcidTissue-type plasminogen activatorsmall moleculeapproved|investigational
TgenePLATP00750DB01088IloprostTissue-type plasminogen activatorsmall moleculeapproved|investigational
TgenePLATP00750DB09213DexibuprofenTissue-type plasminogen activatorsmall moleculeapproved|investigational
TgenePLATP00750DB09228Conestat alfaTissue-type plasminogen activatorbiotechapproved|investigational
TgenePLATP00750DB00013UrokinaseTissue-type plasminogen activatorbiotechapproved|investigational|withdrawn

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RelatedDiseases for MYH9_PLAT


check button Diseases associated with fusion partners.
(DisGeNet 4.0)
PartnerGeneDisease IDDisease name# pubmedsSource
HgeneMYH9C0403445Fechtner syndrome (disorder)9UNIPROT
HgeneMYH9C0398641Epstein syndrome (disorder)7UNIPROT
HgeneMYH9C0340978May-Hegglin anomaly6UNIPROT
HgeneMYH9C0022661Kidney Failure, Chronic2CTD_human
HgeneMYH9C1854520SEBASTIAN SYNDROME2CTD_human;ORPHANET;UNIPROT
HgeneMYH9C0017668Focal glomerulosclerosis1CTD_human
HgeneMYH9C0020544Renal hypertension1CTD_human
HgeneMYH9C0027706Hereditary nephritis1CTD_human
HgeneMYH9C0036341Schizophrenia1PSYGENET
HgeneMYH9C1863659DEAFNESS, AUTOSOMAL DOMINANT 171UNIPROT
HgeneMYH9C2673482Increased susceptibility to schizophrenia1PSYGENET
TgenePLATC0038454Cerebrovascular accident59CTD_human
TgenePLATC0027051Myocardial Infarction35CTD_human
TgenePLATC0007786Brain Ischemia25CTD_human
TgenePLATC2937358Cerebral Hemorrhage21CTD_human
TgenePLATC0151699Intracranial Hemorrhages14CTD_human
TgenePLATC0034065Pulmonary Embolism9CTD_human
TgenePLATC0019080Hemorrhage8CTD_human
TgenePLATC0007785Cerebral Infarction6CTD_human
TgenePLATC0040053Thrombosis4CTD_human
TgenePLATC0740392Infarction, Middle Cerebral Artery4CTD_human
TgenePLATC0002994Angioedema3CTD_human
TgenePLATC0010072Coronary Thrombosis3CTD_human
TgenePLATC0042487Venous Thrombosis3CTD_human
TgenePLATC0007781Intracranial Embolism and Thrombosis2CTD_human
TgenePLATC0877172Hematoma, Epidural, Spinal2CTD_human
TgenePLATC0001125Acidosis, Lactic1CTD_human
TgenePLATC0001883Airway Obstruction1CTD_human
TgenePLATC0003537Aphasia1CTD_human
TgenePLATC0003838Arterial Occlusive Diseases1CTD_human
TgenePLATC0004153Atherosclerosis1CTD_human
TgenePLATC0004604Back Pain1CTD_human
TgenePLATC0004610Bacteremia1CTD_human
TgenePLATC0007177Cardiac Tamponade1CTD_human
TgenePLATC0013922Embolism1CTD_human
TgenePLATC0018801Heart failure1CTD_human
TgenePLATC0018946Hematoma, Subdural1CTD_human
TgenePLATC0020538Hypertensive disease1CTD_human
TgenePLATC0020649Hypotension1CTD_human
TgenePLATC0023893Liver Cirrhosis, Experimental1CTD_human
TgenePLATC0024031Low Back Pain1CTD_human
TgenePLATC0025309Meningoencephalitis1CTD_human
TgenePLATC0027746Nerve Degeneration1CTD_human
TgenePLATC0030552Paresis1CTD_human
TgenePLATC0031039Pericardial effusion1CTD_human
TgenePLATC0033975Psychotic Disorders1PSYGENET
TgenePLATC0035126Reperfusion Injury1CTD_human
TgenePLATC0035229Respiratory Insufficiency1CTD_human
TgenePLATC0036341Schizophrenia1PSYGENET
TgenePLATC0036980Shock, Cardiogenic1CTD_human
TgenePLATC0037926Compression of spinal cord1CTD_human
TgenePLATC0040038Thromboembolism1CTD_human
TgenePLATC0085307Embolism and Thrombosis1CTD_human
TgenePLATC0149649Cholesterol Embolism1CTD_human
TgenePLATC0162820Dermatitis, Allergic Contact1CTD_human
TgenePLATC0235032Neurotoxicity Syndromes1CTD_human
TgenePLATC0236733Amphetamine-Related Disorders1CTD_human
TgenePLATC0242184Hypoxia1CTD_human
TgenePLATC0242698Ventricular Dysfunction, Left1CTD_human
TgenePLATC0349204Nonorganic psychosis1PSYGENET
TgenePLATC0740858Substance abuse problem1PSYGENET
TgenePLATC0751895Vasospasm, Intracranial1CTD_human
TgenePLATC0751955Brain Infarction1CTD_human
TgenePLATC0752143Intracranial Thrombosis1CTD_human
TgenePLATC1861172Venous Thromboembolism1CTD_human
TgenePLATC4277682Chemical and Drug Induced Liver Injury1CTD_human