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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: 39516

FusionGeneSummary for TRIM33_COL24A1

check button Fusion gene summary
Fusion gene informationFusion gene name: TRIM33_COL24A1
Fusion gene ID: 39516
HgeneTgene
Gene symbol

TRIM33

COL24A1

Gene ID

51592

255631

Gene nametripartite motif containing 33collagen type XXIV alpha 1 chain
SynonymsECTO|PTC7|RFG7|TF1G|TIF1G|TIF1GAMMA|TIFGAMMA-
Cytomap

1p13.2

1p22.3

Type of geneprotein-codingprotein-coding
DescriptionE3 ubiquitin-protein ligase TRIM33RET-fused gene 7 proteinRING-type E3 ubiquitin transferase TRIM33TIF1-gammaectodermin homologprotein Rfg7transcriptional intermediary factor 1 gammacollagen alpha-1(XXIV) chaincollagen, type XXIV, alpha 1
Modification date2018052020180523
UniProtAcc

Q9UPN9

Q17RW2

Ensembl transtripts involved in fusion geneENST00000358465, ENST00000369543, 
ENST00000450349, ENST00000476908, 
ENST00000436319, ENST00000370571, 
ENST00000485434, 
Fusion gene scores* DoF score11 X 8 X 9=7924 X 4 X 2=32
# samples 123
** MAII scorelog2(12/792*10)=-2.72246602447109
possibly effective Gene in Pan-Cancer Fusion Genes (peGinPCFGs).
DoF>8 and MAII<0
log2(3/32*10)=-0.0931094043914815
possibly effective Gene in Pan-Cancer Fusion Genes (peGinPCFGs).
DoF>8 and MAII<0
Context

PubMed: TRIM33 [Title/Abstract] AND COL24A1 [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
HgeneTRIM33

GO:0016567

protein ubiquitination

19135894

HgeneTRIM33

GO:0017015

regulation of transforming growth factor beta receptor signaling pathway

19135894

HgeneTRIM33

GO:0030514

negative regulation of BMP signaling pathway

19135894


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-AN-A0FV-01ATRIM33chr1

115005726

-COL24A1chr1

86334309

-
* 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
Frame-shiftENST00000358465ENST00000436319TRIM33chr1

115005726

-COL24A1chr1

86334309

-
Frame-shiftENST00000358465ENST00000370571TRIM33chr1

115005726

-COL24A1chr1

86334309

-
5CDS-intronENST00000358465ENST00000485434TRIM33chr1

115005726

-COL24A1chr1

86334309

-
Frame-shiftENST00000369543ENST00000436319TRIM33chr1

115005726

-COL24A1chr1

86334309

-
Frame-shiftENST00000369543ENST00000370571TRIM33chr1

115005726

-COL24A1chr1

86334309

-
5CDS-intronENST00000369543ENST00000485434TRIM33chr1

115005726

-COL24A1chr1

86334309

-
5UTR-3CDSENST00000450349ENST00000436319TRIM33chr1

115005726

-COL24A1chr1

86334309

-
5UTR-3CDSENST00000450349ENST00000370571TRIM33chr1

115005726

-COL24A1chr1

86334309

-
5UTR-intronENST00000450349ENST00000485434TRIM33chr1

115005726

-COL24A1chr1

86334309

-
intron-3CDSENST00000476908ENST00000436319TRIM33chr1

115005726

-COL24A1chr1

86334309

-
intron-3CDSENST00000476908ENST00000370571TRIM33chr1

115005726

-COL24A1chr1

86334309

-
intron-intronENST00000476908ENST00000485434TRIM33chr1

115005726

-COL24A1chr1

86334309

-

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FusionProtFeatures for TRIM33_COL24A1


check buttonMain function of each fusion partner protein. (from UniProt)
HgeneTgene
TRIM33

Q9UPN9

COL24A1

Q17RW2

Acts as an E3 ubiquitin-protein ligase. Promotes SMAD4ubiquitination, nuclear exclusion and degradation via theubiquitin proteasome pathway. According to PubMed:16751102, doesnot promote a decrease in the level of endogenous SMAD4. May actas a transcriptional repressor. Inhibits the transcriptionalresponse to TGF-beta/BMP signaling cascade. Plays a role in thecontrol of cell proliferation. Its association with SMAD2 andSMAD3 stimulates erythroid differentiation of hematopoieticstem/progenitor (By similarity). Monoubiquitinates SMAD4 and actsas an inhibitor of SMAD4-dependent TGF-beta/BMP signaling cascade(Monoubiquitination of SMAD4 hampers its ability to form a stablecomplex with activated SMAD2/3 resulting in inhibition of TGF-beta/BMP signaling cascade). {ECO:0000250,ECO:0000269|PubMed:10022127, ECO:0000269|PubMed:15820681,ECO:0000269|PubMed:16751102, ECO:0000269|PubMed:19135894}. May participate in regulating type I collagenfibrillogenesis at specific anatomical locations during fetaldevelopment. {ECO:0000269|PubMed:12874293}.

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 TRIM33_COL24A1


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 TRIM33_COL24A1


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
TRIM33NCOR1, TRIM33, TRIM24, SMAD2, SMAD3, TAL1, TCF12, TCF3, LDB1, RUNX1T1, CBFA2T3, SSBP2, SSBP3, SSBP4, LYL1, TCF4, RUNX1, SUPT16H, SSRP1, CDK9, SMAD4, HIST1H3A, ELAVL1, CUL3, UBE2D3, ANAPC1, CDC27, ANAPC4, ANAPC5, CDC16, ANAPC7, CDC23, CDC20, BUB1B, CCNA2, EPAS1, SOX2, UBE2I, CRYAB, SHFM1, ZBTB1, CHD1L, SKIL, DHX33, UBE2N, UBE2E1, FZR1, KLHL20, PSME3, QPRT, RABGGTB, DCAF15, LHX6, MTA1, RFC4, NTRK1, EWSR1, XPO1, FGA, RRM1, SSB, VDAC2, C17orf53, JUN, FOXI1, CTNNB1, NANOG, NLGN3, WDYHV1, ACY1, LMO2, ZNF324B, ZIM2, CNKSR1, HAO2, ERG, FOXA1, TRIM25COL24A1APPBP2


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 TRIM33_COL24A1


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 TRIM33_COL24A1


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