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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: 23030

FusionGeneSummary for MYH9_TXN2

check button Fusion gene summary
Fusion gene informationFusion gene name: MYH9_TXN2
Fusion gene ID: 23030
HgeneTgene
Gene symbol

MYH9

TXN2

Gene ID

4627

25828

Gene namemyosin heavy chain 9thioredoxin 2
SynonymsBDPLT6|DFNA17|EPSTS|FTNS|MHA|NMHC-II-A|NMMHC-IIA|NMMHCACOXPD29|MT-TRX|MTRX|TRX2|TXN
Cytomap

22q12.3

22q12.3

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-Athioredoxin, mitochondrialmitochondrial thioredoxin
Modification date2018052220180527
UniProtAcc

P35579

Q99757

Ensembl transtripts involved in fusion geneENST00000216181, ENST00000475726, 
ENST00000401701, 
ENST00000216185, 
ENST00000416967, ENST00000487725, 
ENST00000403313, 
Fusion gene scores* DoF score36 X 33 X 15=178203 X 4 X 6=72
# samples 507
** MAII scorelog2(50/17820*10)=-5.1554254317472
possibly effective Gene in Pan-Cancer Fusion Genes (peGinPCFGs).
DoF>8 and MAII<0
log2(7/72*10)=-0.0406419844973459
possibly effective Gene in Pan-Cancer Fusion Genes (peGinPCFGs).
DoF>8 and MAII<0
Context

PubMed: MYH9 [Title/Abstract] AND TXN2 [Title/Abstract] AND fusion [Title/Abstract]

Integrated genomic and molecular characterization of cervical cancer (pmid: 28112728)
Functional or gene categories assigned by FusionGDB annotationTumor suppressor gene involved fusion gene, retained protein feature but frameshift.
DDR (DNA damage repair) gene involved fusion gene, in-frame but not retained their domain.
* 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


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-CN-A49A-01AMYH9chr22

36783852

-TXN2chr22

36863964

-
TCGARVLIHCTCGA-BC-A10R-01AMYH9chr22

36783852

-TXN2chr22

36863964

-
TCGARVLUADTCGA-55-8299-01AMYH9chr22

36718474

-TXN2chr22

36876884

-
TCGARVOVTCGA-23-1107-01AMYH9chr22

36783852

-TXN2chr22

36876884

-
TCGARVUCECTCGA-EY-A2ON-01AMYH9chr22

36705327

-TXN2chr22

36863964

-
* 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-3CDSENST00000216181ENST00000216185MYH9chr22

36783852

-TXN2chr22

36863964

-
5UTR-3CDSENST00000216181ENST00000416967MYH9chr22

36783852

-TXN2chr22

36863964

-
5UTR-5UTRENST00000216181ENST00000487725MYH9chr22

36783852

-TXN2chr22

36863964

-
5UTR-5UTRENST00000216181ENST00000403313MYH9chr22

36783852

-TXN2chr22

36863964

-
intron-3CDSENST00000475726ENST00000216185MYH9chr22

36783852

-TXN2chr22

36863964

-
intron-3CDSENST00000475726ENST00000416967MYH9chr22

36783852

-TXN2chr22

36863964

-
intron-5UTRENST00000475726ENST00000487725MYH9chr22

36783852

-TXN2chr22

36863964

-
intron-5UTRENST00000475726ENST00000403313MYH9chr22

36783852

-TXN2chr22

36863964

-
intron-3CDSENST00000401701ENST00000216185MYH9chr22

36783852

-TXN2chr22

36863964

-
intron-3CDSENST00000401701ENST00000416967MYH9chr22

36783852

-TXN2chr22

36863964

-
intron-5UTRENST00000401701ENST00000487725MYH9chr22

36783852

-TXN2chr22

36863964

-
intron-5UTRENST00000401701ENST00000403313MYH9chr22

36783852

-TXN2chr22

36863964

-
Frame-shitENST00000216181ENST00000216185MYH9chr22

36718474

-TXN2chr22

36876884

-
5CDS-intronENST00000216181ENST00000416967MYH9chr22

36718474

-TXN2chr22

36876884

-
5CDS-intronENST00000216181ENST00000487725MYH9chr22

36718474

-TXN2chr22

36876884

-
5CDS-intronENST00000216181ENST00000403313MYH9chr22

36718474

-TXN2chr22

36876884

-
intron-3CDSENST00000475726ENST00000216185MYH9chr22

36718474

-TXN2chr22

36876884

-
intron-intronENST00000475726ENST00000416967MYH9chr22

36718474

-TXN2chr22

36876884

-
intron-intronENST00000475726ENST00000487725MYH9chr22

36718474

-TXN2chr22

36876884

-
intron-intronENST00000475726ENST00000403313MYH9chr22

36718474

-TXN2chr22

36876884

-
intron-3CDSENST00000401701ENST00000216185MYH9chr22

36718474

-TXN2chr22

36876884

-
intron-intronENST00000401701ENST00000416967MYH9chr22

36718474

-TXN2chr22

36876884

-
intron-intronENST00000401701ENST00000487725MYH9chr22

36718474

-TXN2chr22

36876884

-
intron-intronENST00000401701ENST00000403313MYH9chr22

36718474

-TXN2chr22

36876884

-
5UTR-3CDSENST00000216181ENST00000216185MYH9chr22

36783852

-TXN2chr22

36876884

-
5UTR-intronENST00000216181ENST00000416967MYH9chr22

36783852

-TXN2chr22

36876884

-
5UTR-intronENST00000216181ENST00000487725MYH9chr22

36783852

-TXN2chr22

36876884

-
5UTR-intronENST00000216181ENST00000403313MYH9chr22

36783852

-TXN2chr22

36876884

-
intron-3CDSENST00000475726ENST00000216185MYH9chr22

36783852

-TXN2chr22

36876884

-
intron-intronENST00000475726ENST00000416967MYH9chr22

36783852

-TXN2chr22

36876884

-
intron-intronENST00000475726ENST00000487725MYH9chr22

36783852

-TXN2chr22

36876884

-
intron-intronENST00000475726ENST00000403313MYH9chr22

36783852

-TXN2chr22

36876884

-
intron-3CDSENST00000401701ENST00000216185MYH9chr22

36783852

-TXN2chr22

36876884

-
intron-intronENST00000401701ENST00000416967MYH9chr22

36783852

-TXN2chr22

36876884

-
intron-intronENST00000401701ENST00000487725MYH9chr22

36783852

-TXN2chr22

36876884

-
intron-intronENST00000401701ENST00000403313MYH9chr22

36783852

-TXN2chr22

36876884

-
Frame-shitENST00000216181ENST00000216185MYH9chr22

36705327

-TXN2chr22

36863964

-
Frame-shitENST00000216181ENST00000416967MYH9chr22

36705327

-TXN2chr22

36863964

-
5CDS-5UTRENST00000216181ENST00000487725MYH9chr22

36705327

-TXN2chr22

36863964

-
5CDS-5UTRENST00000216181ENST00000403313MYH9chr22

36705327

-TXN2chr22

36863964

-
intron-3CDSENST00000475726ENST00000216185MYH9chr22

36705327

-TXN2chr22

36863964

-
intron-3CDSENST00000475726ENST00000416967MYH9chr22

36705327

-TXN2chr22

36863964

-
intron-5UTRENST00000475726ENST00000487725MYH9chr22

36705327

-TXN2chr22

36863964

-
intron-5UTRENST00000475726ENST00000403313MYH9chr22

36705327

-TXN2chr22

36863964

-
intron-3CDSENST00000401701ENST00000216185MYH9chr22

36705327

-TXN2chr22

36863964

-
intron-3CDSENST00000401701ENST00000416967MYH9chr22

36705327

-TXN2chr22

36863964

-
intron-5UTRENST00000401701ENST00000487725MYH9chr22

36705327

-TXN2chr22

36863964

-
intron-5UTRENST00000401701ENST00000403313MYH9chr22

36705327

-TXN2chr22

36863964

-

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FusionProtFeatures for MYH9_TXN2


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

P35579

TXN2

Q99757

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}. Important for the control of mitochondrial reactiveoxygen species homeostasis, apoptosis regulation and cellviability. Possesses a dithiol-reducing activity.{ECO:0000269|PubMed:12032145, ECO:0000269|PubMed:12080052,ECO:0000269|PubMed:26626369}.

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_TXN2


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_TXN2


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, HDAC6TXN2UCHL5, UBR5, MRPL23, RPL8, RPL9, SNRNP70, PTBP3, GOLIM4, HSPA1L, TOMM22, RPS16, ILF3, ILF2, SPTBN1, TPM4, VCP, MLH1, GPRASP2, ALDOB, SHARPIN, KRT18, VIM, RABAC1, THAP1, NR3C1, RELA, AP2B1, DCTD, MAGEA11, VPS52, TRIM21, TRIP6, ZBTB14, SSNA1, PSME3, STUB1, MAPRE2, MAPRE3, RPIA, MTUS2, RABGEF1, AGTRAP, SCYL3, PPCDC, TIFA, REEP6, CCDC114, MRFAP1L1, KRT40, RBM45, FAM9B, MAP3K5, MOV10, ANXA6, FAM98B, SOD1, TXN, WDR12, TXNIP


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_TXN2


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

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RelatedDiseases for MYH9_TXN2


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
TgeneTXN2C0080178Spina Bifida1CTD_human