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Center for Computational Systems Medicine level1
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Fusion Gene Summary

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Fusion Gene Sample Information

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Fusion ORF Analysis

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Fusion Amino Acid Sequences

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Fusion Protein Functional Features

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Fusion Protein-Protein Interaction

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Related drugs with this fusion protein

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Related disease with this fusion protein

Fusion Protein:MYCBP2-CPB2

Fusion Protein Summary

check button Fusion gene summary
Fusion partner gene informationFusion gene name: MYCBP2-CPB2
FusionPDB ID: 56200
FusionGDB2.0 ID: 56200
HgeneTgene
Gene symbol

MYCBP2

CPB2

Gene ID

23077

1361

Gene nameMYC binding protein 2carboxypeptidase B2
SynonymsMyc-bp2|PAM|PHR1|PhrCPU|PCPB|TAFI
Cytomap

13q22.3

13q14.13

Type of geneprotein-codingprotein-coding
DescriptionE3 ubiquitin-protein ligase MYCBP2HighwireMYC binding protein 2, E3 ubiquitin protein ligasePAM/Highwire/RPM-1 protein 1RING-type E3 ubiquitin transferase MYCBP2myc-binding protein 2pam/highwire/rpm-1 proteinprotein associated with Myccarboxypeptidase B2carboxypeptidase B-like proteincarboxypeptidase B2 (plasma)carboxypeptidase B2 (plasma, carboxypeptidase U)carboxypeptidase Rthrombin-activable fibrinolysis inhibitorthrombin-activatable fibrinolysis inhibitor
Modification date2020031320200313
UniProtAcc

O75592

Q96IY4

Ensembl transtripts involved in fusion geneENST idsENST00000360084, ENST00000357337, 
ENST00000407578, ENST00000544440, 
ENST00000482517, 
ENST00000181383, 
ENST00000439329, 
Fusion gene scores for assessment (based on all fusion genes of FusionGDB 2.0)* DoF score14 X 16 X 8=17922 X 2 X 2=8
# samples 152
** MAII scorelog2(15/1792*10)=-3.57853623156172
possibly effective Gene in Pan-Cancer Fusion Genes (peGinPCFGs).
DoF>8 and MAII<0
log2(2/8*10)=1.32192809488736
Context (manual curation of fusion genes in FusionPDB)

PubMed: MYCBP2 [Title/Abstract] AND CPB2 [Title/Abstract] AND fusion [Title/Abstract]

Most frequent breakpoint (based on all fusion genes of FusionGDB 2.0)MYCBP2(77862296)-CPB2(46638876), # samples:3
Anticipated loss of major functional domain due to fusion event.MYCBP2-CPB2 seems lost the major protein functional domain in Hgene partner, which is a CGC by not retaining the major functional domain in the partially deleted in-frame ORF.
MYCBP2-CPB2 seems lost the major protein functional domain in Hgene partner, which is a CGC by not retaining the major functional domain in the partially deleted in-frame ORF.
MYCBP2-CPB2 seems lost the major protein functional domain in Hgene partner, which is a essential gene by not retaining the major functional domain in the partially deleted in-frame ORF.
MYCBP2-CPB2 seems lost the major protein functional domain in Hgene partner, which is a essential gene by not retaining the major functional domain in the partially deleted in-frame ORF.
MYCBP2-CPB2 seems lost the major protein functional domain in Hgene partner, which is a essential gene due to the frame-shifted ORF.
MYCBP2-CPB2 seems lost the major protein functional domain in Tgene partner, which is a IUPHAR drug target due to the frame-shifted ORF.
* 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
HgeneMYCBP2

GO:0016567

protein ubiquitination

29643511

HgeneMYCBP2

GO:0031398

positive regulation of protein ubiquitination

20534529


check buttonFusion gene breakpoints across MYCBP2 (5'-gene)
* Click on the image to open the UCSC genome browser with custom track showing this image in a new window.
all structure

check buttonFusion gene breakpoints across CPB2 (3'-gene)
* Click on the image to open the UCSC genome browser with custom track showing this image in a new window.
all structure


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Fusion Gene Sample Information

check buttonFusion gene information from FusionGDB2.0.
check button Fusion gene information from two resources (ChiTars 5.0 and ChimerDB 4.0)
* 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.
SourceDiseaseSampleHgeneHchrHbpHstrandTgeneTchrTbpTstrand
ChimerDB4BLCATCGA-UY-A78N-01AMYCBP2chr13

77862296

-CPB2chr13

46638876

-


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Fusion ORF Analysis


check buttonFusion information from ORFfinder translation from full-length transcript sequence from FusionPDB.
HenstTenstHgeneHchrHbpHstrandTgeneTchrTbpTstrandSeq length
(transcript)
BP loci
(transcript)
Predicted start
(transcript)
Predicted stop
(transcript)
Seq length
(amino acids)
ENST00000544440MYCBP2chr1377862296-ENST00000181383CPB2chr1346638876-1496498121067351
ENST00000544440MYCBP2chr1377862296-ENST00000439329CPB2chr1346638876-144349812989325
ENST00000407578MYCBP2chr1377862296-ENST00000181383CPB2chr1346638876-18598611831430415
ENST00000407578MYCBP2chr1377862296-ENST00000439329CPB2chr1346638876-18068611831352389

check buttonDeepORF prediction of the coding potential based on the fusion transcript sequence of in-frame fusion genes. DeepORF is a coding potential classifier based on convolutional neural network by comparing the real Ribo-seq data. If the no-coding score < 0.5 and coding score > 0.5, then the in-frame fusion transcript is predicted as being likely translated.
HenstTenstHgeneHchrHbpHstrandTgeneTchrTbpTstrandNo-coding scoreCoding score
ENST00000544440ENST00000181383MYCBP2chr1377862296-CPB2chr1346638876-0.0010259550.9989741
ENST00000544440ENST00000439329MYCBP2chr1377862296-CPB2chr1346638876-0.0012113240.99878865
ENST00000407578ENST00000181383MYCBP2chr1377862296-CPB2chr1346638876-0.0016039960.998396
ENST00000407578ENST00000439329MYCBP2chr1377862296-CPB2chr1346638876-0.0015445650.9984554

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Fusion Amino Acid Sequences


check button For individual full-length fusion transcript sequence from FusionPDB, we ran ORFfinder and chose the longest ORF among the all predicted ones.
>FusionGDB ID_FusionGDB isoform ID_FGname_Hgene_Hchr_Hbp_Henst_Tgene_Tchr_Tbp_Tenst_length(fusion AA) seq_BP

>56200_56200_1_MYCBP2-CPB2_MYCBP2_chr13_77862296_ENST00000407578_CPB2_chr13_46638876_ENST00000181383_length(amino acids)=415AA_BP=226
MEKGCVCARVSARPARGDEAAAAAAAARMMMCAATASPAAASSGLGGDGFYPAATFSSSPAPGALFMPVPDGSVAAAGLGLGLPAADSRG
HYQLLLSGRALADRYRRIYTAALNDRDQGGGSAGHPASRNKKILNKKKLKRKQKSKSKVKTRSKSENLENTVIIPDIKLHSNPSAFNIYC
NVRHCVLEWQKKEISLAAASKNSVQSGESDSDEEEESKEPPIKLPKNRMWRKNRSFYANNHCIGTDLNRNFASKHWCEEGASSSSCSETY
CGLYPESEPEVKAVASFLRRNINQIKAYISMHSYSQHIVFPYSYTRSKSKDHEELSLVASEAVRAIEKISKNTRYTHGHGSETLYLAPGG

--------------------------------------------------------------

>56200_56200_2_MYCBP2-CPB2_MYCBP2_chr13_77862296_ENST00000407578_CPB2_chr13_46638876_ENST00000439329_length(amino acids)=389AA_BP=226
MEKGCVCARVSARPARGDEAAAAAAAARMMMCAATASPAAASSGLGGDGFYPAATFSSSPAPGALFMPVPDGSVAAAGLGLGLPAADSRG
HYQLLLSGRALADRYRRIYTAALNDRDQGGGSAGHPASRNKKILNKKKLKRKQKSKSKVKTRSKSENLENTVIIPDIKLHSNPSAFNIYC
NVRHCVLEWQKKEISLAAASKNSVQSGESDSDEEEESKEPPIKLPKNRMWRKNRSFYANNHCIGTDLNRNFASKHWCEEGASSSSCSETY
CGLYPESEPEVKAVASFLRRNINQIKAYISMHSYSQHIVFPYSYTRSKSKDHEELSLVASEAVRAIEKISKNTRYTHGHGSETLYLAPGG

--------------------------------------------------------------

>56200_56200_3_MYCBP2-CPB2_MYCBP2_chr13_77862296_ENST00000544440_CPB2_chr13_46638876_ENST00000181383_length(amino acids)=351AA_BP=162
MFMPVPDGSVAAAGLGLGLPAADSRGHYQLLLSGRALADRYRRIYTAALNDRDQGGGSAGHPASRNKKILNKKKLKRKQKSKSKVKTRSK
SENLENTVIIPDIKLHSNPSAFNIYCNVRHCVLEWQKKEISLAAASKNSVQSGESDSDEEEESKEPPIKLPKNRMWRKNRSFYANNHCIG
TDLNRNFASKHWCEEGASSSSCSETYCGLYPESEPEVKAVASFLRRNINQIKAYISMHSYSQHIVFPYSYTRSKSKDHEELSLVASEAVR

--------------------------------------------------------------

>56200_56200_4_MYCBP2-CPB2_MYCBP2_chr13_77862296_ENST00000544440_CPB2_chr13_46638876_ENST00000439329_length(amino acids)=325AA_BP=162
MFMPVPDGSVAAAGLGLGLPAADSRGHYQLLLSGRALADRYRRIYTAALNDRDQGGGSAGHPASRNKKILNKKKLKRKQKSKSKVKTRSK
SENLENTVIIPDIKLHSNPSAFNIYCNVRHCVLEWQKKEISLAAASKNSVQSGESDSDEEEESKEPPIKLPKNRMWRKNRSFYANNHCIG
TDLNRNFASKHWCEEGASSSSCSETYCGLYPESEPEVKAVASFLRRNINQIKAYISMHSYSQHIVFPYSYTRSKSKDHEELSLVASEAVR

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Fusion Protein Functional Features


check button Four levels of functional features of fusion genes
Go to FGviewer search page for the most frequent breakpoint (https://ccsmweb.uth.edu/FGviewer/chr13:77862296/chr13:46638876)
- FGviewer provides the online visualization of the retention search of the protein functional features across DNA, RNA, protein, and pathological levels.
- How to search
1. Put your fusion gene symbol.
2. Press the tab key until there will be shown the breakpoint information filled.
4. Go down and press 'Search' tab twice.
4. Go down to have the hyperlink of the search result.
5. Click the hyperlink.
6. See the FGviewer result for your fusion gene.
FGviewer

check buttonMain function of each fusion partner protein. (from UniProt)
HgeneTgene
MYCBP2

O75592

CPB2

Q96IY4

FUNCTION: Atypical E3 ubiquitin-protein ligase which specifically mediates ubiquitination of threonine and serine residues on target proteins, instead of ubiquitinating lysine residues (PubMed:29643511). Shows esterification activity towards both threonine and serine, with a preference for threonine, and acts via two essential catalytic cysteine residues that relay ubiquitin to its substrate via thioester intermediates (PubMed:29643511). Interacts with the E2 enzymes UBE2D1, UBE2D3, UBE2E1 and UBE2L3 (PubMed:18308511, PubMed:29643511). Plays a key role in neural development, probably by mediating ubiquitination of threonine residues on target proteins (Probable). Involved in different processes such as regulation of neurite outgrowth, synaptic growth, synaptogenesis and axon degeneration (By similarity). Required for the formation of major central nervous system axon tracts (By similarity). Required for proper axon growth by regulating axon navigation and axon branching: acts by regulating the subcellular location and stability of MAP3K12/DLK (By similarity). Required for proper localization of retinogeniculate projections but not for eye-specific segregation (By similarity). Regulates axon guidance in the olfactory system (By similarity). Involved in Wallerian axon degeneration, an evolutionarily conserved process that drives the loss of damaged axons: acts by promoting destabilization of NMNAT2, probably via ubiquitination of NMNAT2 (By similarity). Catalyzes ubiquitination of threonine and/or serine residues on NMNAT2, consequences of threonine and/or serine ubiquitination are however unknown (PubMed:29643511). Regulates the internalization of TRPV1 in peripheral sensory neurons (By similarity). Mediates ubiquitination and subsequent proteasomal degradation of TSC2/tuberin (PubMed:18308511, PubMed:27278822). Independently of the E3 ubiquitin-protein ligase activity, also acts as a guanosine exchange factor (GEF) for RAN in neurons of dorsal root ganglia (PubMed:26304119). May function as a facilitator or regulator of transcriptional activation by MYC (PubMed:9689053). Acts in concert with HUWE1 to regulate the circadian clock gene expression by promoting the lithium-induced ubiquination and degradation of NR1D1 (PubMed:20534529). {ECO:0000250|UniProtKB:Q7TPH6, ECO:0000269|PubMed:18308511, ECO:0000269|PubMed:20534529, ECO:0000269|PubMed:26304119, ECO:0000269|PubMed:27278822, ECO:0000269|PubMed:29643511, ECO:0000269|PubMed:9689053}.FUNCTION: Cleaves C-terminal arginine or lysine residues from biologically active peptides such as kinins or anaphylatoxins in the circulation thereby regulating their activities. Down-regulates fibrinolysis by removing C-terminal lysine residues from fibrin that has already been partially degraded by plasmin. {ECO:0000269|PubMed:10574983}.

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.
- Retained protein feature among the 13 regional features.
PartnerGeneHbpTbpENSTStrandBPexonTotalExonProtein feature loci*BPlociTotalLenProtein featureProtein feature note
HgeneMYCBP2chr13:77862296chr13:46638876ENST00000357337-484103_126160.04641.0Compositional biasLys-rich
HgeneMYCBP2chr13:77862296chr13:46638876ENST00000544440-383103_126160.04641.0Compositional biasLys-rich
TgeneCPB2chr13:77862296chr13:46638876ENST00000181383611256_257234.0424.0RegionSubstrate binding
TgeneCPB2chr13:77862296chr13:46638876ENST00000181383611311_312234.0424.0RegionSubstrate binding

- Not-retained protein feature among the 13 regional features.
PartnerGeneHbpTbpENSTStrandBPexonTotalExonProtein feature loci*BPlociTotalLenProtein featureProtein feature note
HgeneMYCBP2chr13:77862296chr13:46638876ENST00000357337-4842720_2844160.04641.0Compositional biasSer-rich
HgeneMYCBP2chr13:77862296chr13:46638876ENST00000357337-4843194_3215160.04641.0Compositional biasLys-rich
HgeneMYCBP2chr13:77862296chr13:46638876ENST00000357337-4843262_3293160.04641.0Compositional biasNote=Gly-rich
HgeneMYCBP2chr13:77862296chr13:46638876ENST00000357337-484766_814160.04641.0Compositional biasCys-rich
HgeneMYCBP2chr13:77862296chr13:46638876ENST00000544440-3832720_2844160.04641.0Compositional biasSer-rich
HgeneMYCBP2chr13:77862296chr13:46638876ENST00000544440-3833194_3215160.04641.0Compositional biasLys-rich
HgeneMYCBP2chr13:77862296chr13:46638876ENST00000544440-3833262_3293160.04641.0Compositional biasNote=Gly-rich
HgeneMYCBP2chr13:77862296chr13:46638876ENST00000544440-383766_814160.04641.0Compositional biasCys-rich
HgeneMYCBP2chr13:77862296chr13:46638876ENST00000357337-4843719_3897160.04641.0DomainDOC
HgeneMYCBP2chr13:77862296chr13:46638876ENST00000544440-3833719_3897160.04641.0DomainDOC
HgeneMYCBP2chr13:77862296chr13:46638876ENST00000357337-4841235_1386160.04641.0RegionPHR domain 1
HgeneMYCBP2chr13:77862296chr13:46638876ENST00000357337-4841726_1884160.04641.0RegionPHR domain 2
HgeneMYCBP2chr13:77862296chr13:46638876ENST00000357337-4842022_2550160.04641.0RegionRAE1 binding
HgeneMYCBP2chr13:77862296chr13:46638876ENST00000357337-4844539_4676160.04641.0RegionTandem cysteine domain
HgeneMYCBP2chr13:77862296chr13:46638876ENST00000544440-3831235_1386160.04641.0RegionPHR domain 1
HgeneMYCBP2chr13:77862296chr13:46638876ENST00000544440-3831726_1884160.04641.0RegionPHR domain 2
HgeneMYCBP2chr13:77862296chr13:46638876ENST00000544440-3832022_2550160.04641.0RegionRAE1 binding
HgeneMYCBP2chr13:77862296chr13:46638876ENST00000544440-3834539_4676160.04641.0RegionTandem cysteine domain
HgeneMYCBP2chr13:77862296chr13:46638876ENST00000357337-4841010_1066160.04641.0RepeatRCC1 5
HgeneMYCBP2chr13:77862296chr13:46638876ENST00000357337-4842341_2443160.04641.0RepeatFilamin
HgeneMYCBP2chr13:77862296chr13:46638876ENST00000357337-484600_655160.04641.0RepeatRCC1 1
HgeneMYCBP2chr13:77862296chr13:46638876ENST00000357337-484699_755160.04641.0RepeatRCC1 2
HgeneMYCBP2chr13:77862296chr13:46638876ENST00000357337-484907_957160.04641.0RepeatRCC1 3
HgeneMYCBP2chr13:77862296chr13:46638876ENST00000357337-484958_1008160.04641.0RepeatRCC1 4
HgeneMYCBP2chr13:77862296chr13:46638876ENST00000544440-3831010_1066160.04641.0RepeatRCC1 5
HgeneMYCBP2chr13:77862296chr13:46638876ENST00000544440-3832341_2443160.04641.0RepeatFilamin
HgeneMYCBP2chr13:77862296chr13:46638876ENST00000544440-383600_655160.04641.0RepeatRCC1 1
HgeneMYCBP2chr13:77862296chr13:46638876ENST00000544440-383699_755160.04641.0RepeatRCC1 2
HgeneMYCBP2chr13:77862296chr13:46638876ENST00000544440-383907_957160.04641.0RepeatRCC1 3
HgeneMYCBP2chr13:77862296chr13:46638876ENST00000544440-383958_1008160.04641.0RepeatRCC1 4
HgeneMYCBP2chr13:77862296chr13:46638876ENST00000357337-4844428_4479160.04641.0Zinc fingerRING-type%3B atypical
HgeneMYCBP2chr13:77862296chr13:46638876ENST00000544440-3834428_4479160.04641.0Zinc fingerRING-type%3B atypical
TgeneCPB2chr13:77862296chr13:46638876ENST00000181383611181_184234.0424.0RegionSubstrate binding


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Fusion Protein-Protein Interaction


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 from validated records (BIOGRID-3.4.160)
GenePPI interactors


check button Protein-protein interactors based on sequence similarity (STRING)
GeneSTRING network
MYCBP2
CPB2


check button - Retained interactions in fusion protein (protein functional feature from UniProt).
PartnerGeneHbpTbpENSTStrandBPexonTotalExonProtein feature loci*BPlociTotalLenStill interaction with


check button - Lost interactions due to fusion (protein functional feature from UniProt).
PartnerGeneHbpTbpENSTStrandBPexonTotalExonProtein feature loci*BPlociTotalLenInteraction lost with


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Related Drugs to MYCBP2-CPB2


check button Drugs used for this fusion-positive patient.
(Manual curation of PubMed, 04-30-2022 + MyCancerGenome)
HgeneTgeneDrugSourcePMID

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Related Diseases to MYCBP2-CPB2


check button Diseases that have this fusion gene.
(Manual curation of PubMed, 04-30-2022 + MyCancerGenome)
HgeneTgeneDiseaseSourcePMID

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