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Center for Computational Systems Medicine level2
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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 Structure

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pLDDT scores

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Ramachandran Plot of Fusion Protein Structure

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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:CBL-CXCR5

Fusion Protein Summary

check button Fusion gene summary
Fusion partner gene informationFusion gene name: CBL-CXCR5
FusionPDB ID: 13396
FusionGDB2.0 ID: 13396
HgeneTgene
Gene symbol

CBL

CXCR5

Gene ID

867

643

Gene nameCbl proto-oncogeneC-X-C motif chemokine receptor 5
SynonymsC-CBL|CBL2|FRA11B|NSLL|RNF55BLR1|CD185|MDR15
Cytomap

11q23.3

11q23.3

Type of geneprotein-codingprotein-coding
DescriptionE3 ubiquitin-protein ligase CBLCas-Br-M (murine) ecotropic retroviral transforming sequenceCbl proto-oncogene, E3 ubiquitin protein ligaseRING finger protein 55RING-type E3 ubiquitin transferase CBLcasitas B-lineage lymphoma proto-oncogenefragile siC-X-C chemokine receptor type 5Burkitt lymphoma receptor 1, GTP binding protein (chemokine (C-X-C motif) receptor 5)Burkitt lymphoma receptor 1, GTP-binding proteinCXC-R5CXCR-5MDR-15chemokine (C-X-C motif) receptor 5monocyte-derived receptor 15
Modification date2020032720200313
UniProtAcc

Q8IUK8

P32302

Ensembl transtripts involved in fusion geneENST idsENST00000264033, ENST00000292174, 
Fusion gene scores for assessment (based on all fusion genes of FusionGDB 2.0)* DoF score13 X 8 X 8=83212 X 4 X 8=384
# samples 1812
** MAII scorelog2(18/832*10)=-2.20858662181142
possibly effective Gene in Pan-Cancer Fusion Genes (peGinPCFGs).
DoF>8 and MAII<0
log2(12/384*10)=-1.67807190511264
possibly effective Gene in Pan-Cancer Fusion Genes (peGinPCFGs).
DoF>8 and MAII<0
Context (manual curation of fusion genes in FusionPDB)

PubMed: CBL [Title/Abstract] AND CXCR5 [Title/Abstract] AND fusion [Title/Abstract]

Most frequent breakpoint (based on all fusion genes of FusionGDB 2.0)CBL(119103405)-CXCR5(118764305), # samples:3
Anticipated loss of major functional domain due to fusion event.CBL-CXCR5 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.
CBL-CXCR5 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.
* 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 buttonFusion gene breakpoints across CBL (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 CXCR5 (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
ChimerDB4PRADTCGA-J9-A8CL-01ACBLchr11

119103405

-CXCR5chr11

118764305

+
ChimerDB4PRADTCGA-J9-A8CL-01ACBLchr11

119103405

+CXCR5chr11

118764305

+
ChimerDB4PRADTCGA-J9-A8CLCBLchr11

119103405

+CXCR5chr11

118764305

+


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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)
ENST00000264033CBLchr11119103405+ENST00000292174CXCR5chr11118764305+50238198281886352

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
ENST00000264033ENST00000292174CBLchr11119103405+CXCR5chr11118764305+0.0862961040.9137039

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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

>13396_13396_1_CBL-CXCR5_CBL_chr11_119103405_ENST00000264033_CXCR5_chr11_118764305_ENST00000292174_length(amino acids)=352AA_BP=
MDRLDNYNDTSLVENHLCPATEGPLMASFKAVFVPVAYSLIFLLGVIGNVLVLVILERHRQTRSSTETFLFHLAVADLLLVFILPFAVAE
GSVGWVLGTFLCKTVIALHKVNFYCSSLLLACIAVDRYLAIVHAVHAYRHRRLLSIHITCGTIWLVGFLLALPEILFAKVSQGHHNNSLP
RCTFSQENQAETHAWFTSRFLYHVAGFLLPMLVMGWCYVGVVHRLRQAQRRPQRQKAVRVAILVTSIFFLCWSPYHIVIFLDTLARLKAV

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

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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/chr11:119103405/chr11:118764305)
- 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
CBL

Q8IUK8

CXCR5

P32302

FUNCTION: Acts as a synaptic organizer in specific subsets of neurons in the brain (By similarity). Essential for long-term maintenance but not establishment of excitatory synapses (By similarity). {ECO:0000250|UniProtKB:Q8BGU2}.FUNCTION: Cytokine receptor that binds to B-lymphocyte chemoattractant (BLC). Involved in B-cell migration into B-cell follicles of spleen and Peyer patches but not into those of mesenteric or peripheral lymph nodes. May have a regulatory function in Burkitt lymphoma (BL) lymphomagenesis and/or B-cell differentiation.

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
TgeneCXCR5chr11:119103405chr11:118764305ENST0000029217402110_12417.0373.0Topological domainExtracellular
TgeneCXCR5chr11:119103405chr11:118764305ENST0000029217402146_16717.0373.0Topological domainCytoplasmic
TgeneCXCR5chr11:119103405chr11:118764305ENST0000029217402189_21917.0373.0Topological domainExtracellular
TgeneCXCR5chr11:119103405chr11:118764305ENST0000029217402241_25917.0373.0Topological domainCytoplasmic
TgeneCXCR5chr11:119103405chr11:118764305ENST0000029217402281_30417.0373.0Topological domainExtracellular
TgeneCXCR5chr11:119103405chr11:118764305ENST0000029217402326_37217.0373.0Topological domainCytoplasmic
TgeneCXCR5chr11:119103405chr11:118764305ENST000002921740277_8817.0373.0Topological domainCytoplasmic
TgeneCXCR5chr11:119103405chr11:118764305ENST0000029217402125_14517.0373.0TransmembraneHelical%3B Name%3D3
TgeneCXCR5chr11:119103405chr11:118764305ENST0000029217402168_18817.0373.0TransmembraneHelical%3B Name%3D4
TgeneCXCR5chr11:119103405chr11:118764305ENST0000029217402220_24017.0373.0TransmembraneHelical%3B Name%3D5
TgeneCXCR5chr11:119103405chr11:118764305ENST0000029217402260_28017.0373.0TransmembraneHelical%3B Name%3D6
TgeneCXCR5chr11:119103405chr11:118764305ENST0000029217402305_32517.0373.0TransmembraneHelical%3B Name%3D7
TgeneCXCR5chr11:119103405chr11:118764305ENST000002921740256_7617.0373.0TransmembraneHelical%3B Name%3D1
TgeneCXCR5chr11:119103405chr11:118764305ENST000002921740289_10917.0373.0TransmembraneHelical%3B Name%3D2

- Not-retained protein feature among the 13 regional features.
PartnerGeneHbpTbpENSTStrandBPexonTotalExonProtein feature loci*BPlociTotalLenProtein featureProtein feature note
HgeneCBLchr11:119103405chr11:118764305ENST00000264033+216227_240147.66666666666666907.0Calcium binding.
HgeneCBLchr11:119103405chr11:118764305ENST00000264033+216357_476147.66666666666666907.0Compositional biasNote=Asp/Glu-rich (acidic)
HgeneCBLchr11:119103405chr11:118764305ENST00000264033+216477_688147.66666666666666907.0Compositional biasNote=Pro-rich
HgeneCBLchr11:119103405chr11:118764305ENST00000264033+216689_834147.66666666666666907.0Compositional biasNote=Asp/Glu-rich (acidic)
HgeneCBLchr11:119103405chr11:118764305ENST00000264033+21647_351147.66666666666666907.0DomainCbl-PTB
HgeneCBLchr11:119103405chr11:118764305ENST00000264033+216856_895147.66666666666666907.0DomainUBA
HgeneCBLchr11:119103405chr11:118764305ENST00000264033+216176_248147.66666666666666907.0RegionNote=EF-hand-like
HgeneCBLchr11:119103405chr11:118764305ENST00000264033+216249_351147.66666666666666907.0RegionNote=SH2-like
HgeneCBLchr11:119103405chr11:118764305ENST00000264033+216352_380147.66666666666666907.0RegionNote=Linker
HgeneCBLchr11:119103405chr11:118764305ENST00000264033+216358_906147.66666666666666907.0RegionRequired for ubiquitination of SPRED2
HgeneCBLchr11:119103405chr11:118764305ENST00000264033+21647_175147.66666666666666907.0RegionNote=4H
HgeneCBLchr11:119103405chr11:118764305ENST00000264033+216381_420147.66666666666666907.0Zinc fingerRING-type
TgeneCXCR5chr11:119103405chr11:118764305ENST00000292174021_5517.0373.0Topological domainExtracellular


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Fusion Protein Structures

check button PDB and CIF files of the predicted fusion proteins
* Here we show the 3D structure of the fusion proteins using Mol*. AlphaFold produces a per-residue confidence score (pLDDT) between 0 and 100. Model confidence is shown from the pLDDT values per residue. pLDDT corresponds to the model’s prediction of its score on the local Distance Difference Test. It is a measure of local accuracy (from AlphfaFold website). To color code individual residues, we transformed individual PDB files into CIF format.
Fusion protein PDB link (fusion AA seq ID in FusionPDB)HgeneHchrHbpHstrandTgeneTchrTbpTstrandAA seqLen(AA seq)
PDB file >>>682_CBL_119103405_CXCR5_118764305_ranked_0.pdbCBL119103405119103405ENST00000292174CXCR5chr11118764305+
MDRLDNYNDTSLVENHLCPATEGPLMASFKAVFVPVAYSLIFLLGVIGNVLVLVILERHRQTRSSTETFLFHLAVADLLLVFILPFAVAE
GSVGWVLGTFLCKTVIALHKVNFYCSSLLLACIAVDRYLAIVHAVHAYRHRRLLSIHITCGTIWLVGFLLALPEILFAKVSQGHHNNSLP
RCTFSQENQAETHAWFTSRFLYHVAGFLLPMLVMGWCYVGVVHRLRQAQRRPQRQKAVRVAILVTSIFFLCWSPYHIVIFLDTLARLKAV
352


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pLDDT score distribution

check button pLDDT score distribution of the predicted wild-type structures of two partner proteins from AlphaFold2
* AlphaFold produces a per-residue confidence score (pLDDT) between 0 and 100.
CBL_pLDDT.png
all structure
all structure
CXCR5_pLDDT.png
all structure
all structure

check button pLDDT score distribution of the predicted fusion protein structures from AlphaFold2
* AlphaFold produces a per-residue confidence score (pLDDT) between 0 and 100.
all structure


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Ramachandran Plot of Fusion Protein Structure


check button Ramachandran plot of the torsional angles - phi (φ)and psi (ψ) - of the residues (amino acids) contained in this fusion protein peptide.
Fusion AA seq ID in FusionPDB and their Ramachandran plots

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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
CBLall structure
CXCR5


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
HgeneCBLchr11:119103405chr11:118764305ENST00000264033+216648_906147.66666666666666907.0CD2AP


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Related Drugs to CBL-CXCR5


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 CBL-CXCR5


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
HgeneCBLC3150803NOONAN SYNDROME-LIKE DISORDER WITH OR WITHOUT JUVENILE MYELOMONOCYTIC LEUKEMIA8CTD_human;GENOMICS_ENGLAND;ORPHANET;UNIPROT
HgeneCBLC0349639Juvenile Myelomonocytic Leukemia5CTD_human;GENOMICS_ENGLAND;ORPHANET
HgeneCBLC0008073Developmental Disabilities1CTD_human
HgeneCBLC0010417Cryptorchidism1CTD_human
HgeneCBLC0018273Growth Disorders1CTD_human
HgeneCBLC0021364Male infertility1CTD_human
HgeneCBLC0028326Noonan Syndrome1GENOMICS_ENGLAND
HgeneCBLC0042384Vasculitis1CTD_human
HgeneCBLC0085996Child Development Deviations1CTD_human
HgeneCBLC0085997Child Development Disorders, Specific1CTD_human
HgeneCBLC0431663Bilateral Cryptorchidism1CTD_human
HgeneCBLC0431664Unilateral Cryptorchidism1CTD_human
HgeneCBLC0848676Subfertility, Male1CTD_human
HgeneCBLC0917731Male sterility1CTD_human
HgeneCBLC1563730Abdominal Cryptorchidism1CTD_human
HgeneCBLC1563731Inguinal Cryptorchidism1CTD_human
HgeneCBLC4230920Fetal hydrops (in some patients)1GENOMICS_ENGLAND