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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: 30353

FusionGeneSummary for RANBP9_TPMT

check button Fusion gene summary
Fusion gene informationFusion gene name: RANBP9_TPMT
Fusion gene ID: 30353
HgeneTgene
Gene symbol

RANBP9

TPMT

Gene ID

10048

7172

Gene nameRAN binding protein 9thiopurine S-methyltransferase
SynonymsBPM-L|BPM90|RANBPM|RanBP7TPMTD
Cytomap

6p23

6p22.3

Type of geneprotein-codingprotein-coding
Descriptionran-binding protein 9Ran Binding Protein in the Microtubule organizing centernovel centrosomal protein RanBPMran binding protein, centrosomalran-binding protein Mthiopurine S-methyltransferaseS-adenosyl-L-methionine:thiopurine S-methyltransferase
Modification date2018052220180523
UniProtAcc

Q96S59

P51580

Ensembl transtripts involved in fusion geneENST00000011619, ENST00000469916, 
ENST00000539980, 
ENST00000309983, 
Fusion gene scores* DoF score9 X 4 X 4=1445 X 1 X 4=20
# samples 65
** MAII scorelog2(6/144*10)=-1.26303440583379
possibly effective Gene in Pan-Cancer Fusion Genes (peGinPCFGs).
DoF>8 and MAII<0
log2(5/20*10)=1.32192809488736
effective Gene in Pan-Cancer Fusion Genes (eGinPCFGs).
DoF>8 and MAII>0
Context

PubMed: RANBP9 [Title/Abstract] AND TPMT [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
TgeneTPMT

GO:0017144

drug metabolic process

657528|18484748


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
TCGARVBRCATCGA-C8-A12U-01ARANBP9chr6

13711167

-TPMTchr6

18149402

-
* 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-5UTRENST00000011619ENST00000309983RANBP9chr6

13711167

-TPMTchr6

18149402

-
intron-5UTRENST00000469916ENST00000309983RANBP9chr6

13711167

-TPMTchr6

18149402

-
intron-5UTRENST00000539980ENST00000309983RANBP9chr6

13711167

-TPMTchr6

18149402

-

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FusionProtFeatures for RANBP9_TPMT


check buttonMain function of each fusion partner protein. (from UniProt)
HgeneTgene
RANBP9

Q96S59

TPMT

P51580

May act as an adapter protein to couple membranereceptors to intracellular signaling pathways. May be involved insignaling of ITGB2/LFA-1 and other integrins. Enhances HGF-METsignaling by recruiting Sos and activating the Ras pathway.Enhances dihydrotestosterone-induced transactivation activity ofAR, as well as dexamethasone-induced transactivation activity ofNR3C1, but not affect estrogen-induced transactivation. StabilizesTP73 isoform Alpha, probably by inhibiting its ubiquitination, andincreases its proapoptotic activity. Inhibits the kinase activityof DYRK1A and DYRK1B. Inhibits FMR1 binding to RNA.{ECO:0000269|PubMed:12147692, ECO:0000269|PubMed:12361945,ECO:0000269|PubMed:14500717, ECO:0000269|PubMed:14722085,ECO:0000269|PubMed:15381419, ECO:0000269|PubMed:15558019,ECO:0000269|PubMed:18222118}.

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 RANBP9_TPMT


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 RANBP9_TPMT


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
RANBP9USP11, AR, S100A7, RNPS1, NR3C1, DYRK1B, DISC1, CALB1, UCHL1, MET, HIPK2, RAN, GID8, MPHOSPH8, MKLN1, USP42, PMS1, AIRE, WNK1, APC, PRKACA, TP73, TRAF6, UBC, NCOR2, NCOA6, PPARD, HNF4G, MAPK6, LLGL1, PPP1CA, ARRB1, SPP1, GRK5, MAEA, RMND5A, RANBP9, DDX1, DYNC1H1, DCTN2, PSMC3, DDB1, DCTN1, EEF1A1, BRCA1, NOTCH1, PPP1CC, SMAD9, SMAD3, SMAD2, SPAG8, SOX2, CLEC7A, LTB4R2, TGFBR1, PSMD13, RPS12, RPS13, RPS27, RPS27L, WDR26, TSR1, UBE2I, CBS, HDAC6, FXR1, LRP1, APP, BACE1, HMBS, ADAP1, ADAP2, ITGB2, CD4, ITGB1, TFRC, THRB, THRA, ESR1, L1CAM, PRKCD, PRKCG, DRD1, NTRK2, ENTPD1, CDK11B, FMR1, COPS5, CACNA1G, AXL, RAF1, OPRM1, TP53, GDNF, GLIPR1L2, MMP7, SFRP2, TDGF1, MRPL4, HLA-DPB1, PRG2, EPB41L3, UNK, NTRK1, MED4, EXOC2, CCND1, ILK, NAF1, SKI, TUBA1B, NFATC1, NFATC2, ATM, PIGT, PRG3, BMP1, RANBP10, YPEL5, ARMC8, RMND5B, GID4, ZMYND19, DDX5, RAB8A, EFHC2, PRPF31, LMNATPMTAPP


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 RANBP9_TPMT


check button Drugs targeting genes involved in this fusion gene.
(DrugBank Version 5.1.0 2018-04-02)
PartnerGeneUniProtAccDrugBank IDDrug nameDrug activityDrug typeDrug status
TgeneTPMTP51580DB01250OlsalazineThiopurine S-methyltransferase {ECO:0000303|PubMed:18484748}small moleculeapproved

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RelatedDiseases for RANBP9_TPMT


check button Diseases associated with fusion partners.
(DisGeNet 4.0)
PartnerGeneDisease IDDisease name# pubmedsSource
HgeneRANBP9C0036341Schizophrenia1PSYGENET
TgeneTPMTC0023530Leukopenia3CTD_human
TgeneTPMTC0027947Neutropenia1CTD_human
TgeneTPMTC2750088HEARING LOSS, CISPLATIN-INDUCED, SUSCEPTIBILITY TO1CTD_human