FusionGDB Logo

Home

Download

Statistics

Examples

Help

Contact

Center for Computational Systems Medicine
leaf

FusionGeneSummary

leaf

FusionProtFeature

leaf

FusionGeneSequence

leaf

FusionGenePPI

leaf

RelatedDrugs

leaf

RelatedDiseases

Fusion gene ID: 21375

FusionGeneSummary for MDM1_RBMS2

check button Fusion gene summary
Fusion gene informationFusion gene name: MDM1_RBMS2
Fusion gene ID: 21375
HgeneTgene
Gene symbol

MDM1

RBMS2

Gene ID

56890

5939

Gene nameMdm1 nuclear proteinRNA binding motif single stranded interacting protein 2
Synonyms-SCR3
Cytomap

12q15

12q13.3

Type of geneprotein-codingprotein-coding
Descriptionnuclear protein MDM1Mdm4, transformed 3T3 cell double minute 1, p53 binding proteinnuclear protein double minute 1RNA-binding motif, single-stranded-interacting protein 2suppressor of CDC2 with RNA-binding motif 3
Modification date2018052320180523
UniProtAcc

Q8TC05

Q15434

Ensembl transtripts involved in fusion geneENST00000540418, ENST00000303145, 
ENST00000411698, ENST00000393543, 
ENST00000430606, ENST00000545724, 
ENST00000262031, ENST00000552247, 
ENST00000549945, ENST00000550726, 
ENST00000542360, 
Fusion gene scores* DoF score8 X 6 X 3=1442 X 2 X 2=8
# samples 72
** MAII scorelog2(7/144*10)=-1.04064198449735
possibly effective Gene in Pan-Cancer Fusion Genes (peGinPCFGs).
DoF>8 and MAII<0
log2(2/8*10)=1.32192809488736
Context

PubMed: MDM1 [Title/Abstract] AND RBMS2 [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

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
TCGARVSARCTCGA-DX-A1KU-01AMDM1chr12

68726008

-RBMS2chr12

56974968

+
* 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-3CDSENST00000540418ENST00000262031MDM1chr12

68726008

-RBMS2chr12

56974968

+
5UTR-3CDSENST00000540418ENST00000552247MDM1chr12

68726008

-RBMS2chr12

56974968

+
5UTR-intronENST00000540418ENST00000549945MDM1chr12

68726008

-RBMS2chr12

56974968

+
5UTR-intronENST00000540418ENST00000550726MDM1chr12

68726008

-RBMS2chr12

56974968

+
5UTR-intronENST00000540418ENST00000542360MDM1chr12

68726008

-RBMS2chr12

56974968

+
Frame-shiftENST00000303145ENST00000262031MDM1chr12

68726008

-RBMS2chr12

56974968

+
Frame-shiftENST00000303145ENST00000552247MDM1chr12

68726008

-RBMS2chr12

56974968

+
5CDS-intronENST00000303145ENST00000549945MDM1chr12

68726008

-RBMS2chr12

56974968

+
5CDS-intronENST00000303145ENST00000550726MDM1chr12

68726008

-RBMS2chr12

56974968

+
5CDS-intronENST00000303145ENST00000542360MDM1chr12

68726008

-RBMS2chr12

56974968

+
Frame-shiftENST00000411698ENST00000262031MDM1chr12

68726008

-RBMS2chr12

56974968

+
Frame-shiftENST00000411698ENST00000552247MDM1chr12

68726008

-RBMS2chr12

56974968

+
5CDS-intronENST00000411698ENST00000549945MDM1chr12

68726008

-RBMS2chr12

56974968

+
5CDS-intronENST00000411698ENST00000550726MDM1chr12

68726008

-RBMS2chr12

56974968

+
5CDS-intronENST00000411698ENST00000542360MDM1chr12

68726008

-RBMS2chr12

56974968

+
Frame-shiftENST00000393543ENST00000262031MDM1chr12

68726008

-RBMS2chr12

56974968

+
Frame-shiftENST00000393543ENST00000552247MDM1chr12

68726008

-RBMS2chr12

56974968

+
5CDS-intronENST00000393543ENST00000549945MDM1chr12

68726008

-RBMS2chr12

56974968

+
5CDS-intronENST00000393543ENST00000550726MDM1chr12

68726008

-RBMS2chr12

56974968

+
5CDS-intronENST00000393543ENST00000542360MDM1chr12

68726008

-RBMS2chr12

56974968

+
Frame-shiftENST00000430606ENST00000262031MDM1chr12

68726008

-RBMS2chr12

56974968

+
Frame-shiftENST00000430606ENST00000552247MDM1chr12

68726008

-RBMS2chr12

56974968

+
5CDS-intronENST00000430606ENST00000549945MDM1chr12

68726008

-RBMS2chr12

56974968

+
5CDS-intronENST00000430606ENST00000550726MDM1chr12

68726008

-RBMS2chr12

56974968

+
5CDS-intronENST00000430606ENST00000542360MDM1chr12

68726008

-RBMS2chr12

56974968

+
5UTR-3CDSENST00000545724ENST00000262031MDM1chr12

68726008

-RBMS2chr12

56974968

+
5UTR-3CDSENST00000545724ENST00000552247MDM1chr12

68726008

-RBMS2chr12

56974968

+
5UTR-intronENST00000545724ENST00000549945MDM1chr12

68726008

-RBMS2chr12

56974968

+
5UTR-intronENST00000545724ENST00000550726MDM1chr12

68726008

-RBMS2chr12

56974968

+
5UTR-intronENST00000545724ENST00000542360MDM1chr12

68726008

-RBMS2chr12

56974968

+

Top

FusionProtFeatures for MDM1_RBMS2


check buttonMain function of each fusion partner protein. (from UniProt)
HgeneTgene
MDM1

Q8TC05

RBMS2

Q15434

Microtubule-binding protein that negatively regulatescentriole duplication. Binds to and stabilizes microtubules(PubMed:26337392). {ECO:0000269|PubMed:26337392}.

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


Top

FusionGeneSequence for MDM1_RBMS2


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).

Top

FusionGenePPI for MDM1_RBMS2


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
MDM1HDAC8, MAGEA4, UBE3A, POC1ARBMS2FAM69B, CUL3, TRA2B, TSR1, SYNCRIP, EIF4H, DDX28, MRPL16, SRSF3, MYC, SRPK1, ENO1, MOV10, NXF1, XPO1, ELAVL2, RBFOX2, G3BP1


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


Top

RelatedDrugs for MDM1_RBMS2


check button Drugs targeting genes involved in this fusion gene.
(DrugBank Version 5.1.0 2018-04-02)
PartnerGeneUniProtAccDrugBank IDDrug nameDrug activityDrug typeDrug status

Top

RelatedDiseases for MDM1_RBMS2


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