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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: 10878

FusionGeneSummary for ECD_MRPS16

check button Fusion gene summary
Fusion gene informationFusion gene name: ECD_MRPS16
Fusion gene ID: 10878
HgeneTgene
Gene symbol

ECD

MRPS16

Gene ID

11319

51021

Gene nameecdysoneless cell cycle regulatormitochondrial ribosomal protein S16
SynonymsGCR2|HSGT1|SGT1CGI-132|COXPD2|MRP-S16|RPMS16
Cytomap

10q22.2

10q22.2

Type of geneprotein-codingprotein-coding
Descriptionprotein ecdysoneless homologecdysoneless homologhuman suppressor of GCR twoprotein SGT1suppressor of GCR2suppressor of S. cerevisiae gcr228S ribosomal protein S16, mitochondrialS16mtmitochondrial small ribosomal subunit protein bS16m
Modification date2018052320180523
UniProtAcc

O95905

Q9Y3D3

Ensembl transtripts involved in fusion geneENST00000372979, ENST00000454759, 
ENST00000430082, ENST00000610256, 
ENST00000416782, ENST00000479005, 
ENST00000372945, ENST00000372940, 
Fusion gene scores* DoF score4 X 3 X 3=362 X 2 X 2=8
# samples 42
** MAII scorelog2(4/36*10)=0.15200309344505
effective Gene in Pan-Cancer Fusion Genes (eGinPCFGs).
DoF>8 and MAII>0
log2(2/8*10)=1.32192809488736
Context

PubMed: ECD [Title/Abstract] AND MRPS16 [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
HgeneECD

GO:0045944

positive regulation of transcription by RNA polymerase II

19919181


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
TCGALDLIHCTCGA-DD-AADN-01AECDchr10

74894361

-MRPS16chr10

75010749

-
* 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-intronENST00000372979ENST00000416782ECDchr10

74894361

-MRPS16chr10

75010749

-
intron-5UTRENST00000372979ENST00000479005ECDchr10

74894361

-MRPS16chr10

75010749

-
intron-5UTRENST00000372979ENST00000372945ECDchr10

74894361

-MRPS16chr10

75010749

-
intron-intronENST00000372979ENST00000372940ECDchr10

74894361

-MRPS16chr10

75010749

-
intron-intronENST00000454759ENST00000416782ECDchr10

74894361

-MRPS16chr10

75010749

-
intron-5UTRENST00000454759ENST00000479005ECDchr10

74894361

-MRPS16chr10

75010749

-
intron-5UTRENST00000454759ENST00000372945ECDchr10

74894361

-MRPS16chr10

75010749

-
intron-intronENST00000454759ENST00000372940ECDchr10

74894361

-MRPS16chr10

75010749

-
intron-intronENST00000430082ENST00000416782ECDchr10

74894361

-MRPS16chr10

75010749

-
intron-5UTRENST00000430082ENST00000479005ECDchr10

74894361

-MRPS16chr10

75010749

-
intron-5UTRENST00000430082ENST00000372945ECDchr10

74894361

-MRPS16chr10

75010749

-
intron-intronENST00000430082ENST00000372940ECDchr10

74894361

-MRPS16chr10

75010749

-
intron-intronENST00000610256ENST00000416782ECDchr10

74894361

-MRPS16chr10

75010749

-
intron-5UTRENST00000610256ENST00000479005ECDchr10

74894361

-MRPS16chr10

75010749

-
intron-5UTRENST00000610256ENST00000372945ECDchr10

74894361

-MRPS16chr10

75010749

-
intron-intronENST00000610256ENST00000372940ECDchr10

74894361

-MRPS16chr10

75010749

-

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FusionProtFeatures for ECD_MRPS16


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

O95905

MRPS16

Q9Y3D3

Regulator of p53/TP53 stability and function. InhibitsMDM2-mediated degradation of p53/TP53 possibly by cooperating inpart with TXNIP (PubMed:16849563, PubMed:23880345). May beinvolved transcriptional regulation. In vitro has intrinsictransactivation activity enhanced by EP300. May be atranscriptional activator required for the expression ofglycolytic genes (PubMed:19919181, PubMed:9928932). Involved inregulation of cell cycle progression. Proposed to disrupt Rb-E2Fbinding leading to transcriptional activation of E2F proteins(PubMed:19640839). The cell cycle -regulating function may dependon its RUVBL1-mediated association with the R2TP complex(PubMed:26711270). May play a role in regulation of pre-mRNAsplicing (PubMed:24722212). {ECO:0000269|PubMed:16849563,ECO:0000269|PubMed:19640839, ECO:0000269|PubMed:19919181,ECO:0000269|PubMed:23880345, ECO:0000269|PubMed:26711270,ECO:0000305|PubMed:24722212, ECO:0000305|PubMed:9928932}.

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 ECD_MRPS16


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 ECD_MRPS16


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
ECDNR3C1, EWSR1, PSEN2, PRPF8, PSMD1, PSMC5, PSMD2, PSMC3, TXNIP, TP53, GCFC2, VTI1B, TSSC4, EAPP, SNRNP40, PNKD, AAR2, PTGER3, LIPH, MED4, AHI1, KIAA0753, CEP128, CEP44, CEP63, NPHP1, CEP19, POC1A, RPGRIP1, XPO1, GRIA2, PDK3, MED12, ANAPC15, PIH1D1, CSNK2A1, RUVBL1, TTC27, MYH7, KIAA1143, GPBP1L1, WDR83, GPR156, SNRNP200, ZNHIT2, LYPD4, NCDN, CD2BP2, ECD, EFTUD2, NONO, PARP1, POLR1A, PRPF19, SART3, SLC7A6OS, WDR92MRPS16ICT1, ELAVL1, ZP3, CAND1, ATXN10, MRPS2, MRPS9, MRPS26, MRPS25, MCAT, SLC25A5, HNRNPU, FAM50B, SSBP1, PSMC1, PSMA5, HNRNPDL, PSMC2, HNRNPR, MPV17, PSMA7, CEP76, TRMT10B, PSMD7, COQ4, ADCK3, FAM136A, CDC14B, DUSP11, SBF1, MRPS34, MRPS27, RRS1


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 ECD_MRPS16


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

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RelatedDiseases for ECD_MRPS16


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