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Center for Computational Systems Medicine
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Fusion Gene Summary

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Fusion Gene ORF analysis

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Fusion Genomic Features

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Fusion Protein Features

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Fusion Gene Sequence

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Fusion Gene PPI analysis

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Related Drugs

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Related Diseases

Fusion gene:HBB-RPL3 (FusionGDB2 ID:HG3043TG6122)

Fusion Gene Summary for HBB-RPL3

check button Fusion gene summary
Fusion gene informationFusion gene name: HBB-RPL3
Fusion gene ID: hg3043tg6122
HgeneTgene
Gene symbol

HBB

RPL3

Gene ID

3043

6122

Gene namehemoglobin subunit betaribosomal protein L3
SynonymsCD113t-C|ECYT6|beta-globinASC-1|L3|TARBP-B
Cytomap('HBB')('RPL3')

11p15.4

22q13.1

Type of geneprotein-codingprotein-coding
Descriptionhemoglobin subunit betabeta globin chainhemoglobin beta subunithemoglobin, beta60S ribosomal protein L3HIV-1 TAR RNA-binding protein Blarge ribosomal subunit protein uL3
Modification date2020031320200313
UniProtAcc

P68871

.
Ensembl transtripts involved in fusion geneENST00000335295, 
Fusion gene scores* DoF score6 X 5 X 2=6015 X 13 X 7=1365
# samples 516
** MAII scorelog2(5/60*10)=-0.263034405833794
possibly effective Gene in Pan-Cancer Fusion Genes (peGinPCFGs).
DoF>8 and MAII<0
log2(16/1365*10)=-3.09275714091985
possibly effective Gene in Pan-Cancer Fusion Genes (peGinPCFGs).
DoF>8 and MAII<0
Context

PubMed: HBB [Title/Abstract] AND RPL3 [Title/Abstract] AND fusion [Title/Abstract]

Most frequent breakpointHBB(5248198)-RPL3(39713632), # samples:1
Anticipated loss of major functional domain due to fusion event.
* 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
HgeneHBB

GO:0010942

positive regulation of cell death

19740759

HgeneHBB

GO:0042542

response to hydrogen peroxide

19740759

HgeneHBB

GO:0042744

hydrogen peroxide catabolic process

19740759



check button Fusion gene information
* 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
ChimerDB4Non-CancerERR315333HBBchr11

5248198

-RPL3chr22

39713632

-


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Fusion Gene ORF analysis for HBB-RPL3

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-3CDSENST00000335295ENST00000216146HBBchr11

5248198

-RPL3chr22

39713632

-
intron-5UTRENST00000335295ENST00000401609HBBchr11

5248198

-RPL3chr22

39713632

-
intron-5UTRENST00000335295ENST00000465618HBBchr11

5248198

-RPL3chr22

39713632

-

check buttonORFfinder result based on the fusion transcript sequence of in-frame fusion genes.
HenstTenstHgeneHchrHbpHstrandTgeneTchrTbpTstrandSeq length
(transcript)
BP loci
(transcript)
Predicted start
(transcript)
Predicted stop
(transcript)
Seq length
(amino acids)

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

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Fusion Genomic Features for HBB-RPL3


check buttonFusionAI prediction of the potential fusion gene breakpoint based on the pre-mature RNA sequence context (+/- 5kb of individual partner genes, total 20kb length sequence). FusionAI is a fusion gene breakpoint classifier based on convolutional neural network by comparing the fusion positive and negative sequence context of ~ 20K fusion gene data. From here, we can have the relative potentency of the 20K genomic sequence how individual sequnce will be likely used as the gene fusion breakpoints.
HgeneHchrHbpHstrandTgeneTchrTbpTstrand1-pp (fusion gene breakpoint)


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Fusion Protein Features for HBB-RPL3


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/:5248198/:39713632)
- 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
HBB

P68871

.
FUNCTION: Involved in oxygen transport from the lung to the various peripheral tissues. {ECO:0000269|PubMed:28066926}.; FUNCTION: LVV-hemorphin-7 potentiates the activity of bradykinin, causing a decrease in blood pressure.; FUNCTION: [Spinorphin]: functions as an endogenous inhibitor of enkephalin-degrading enzymes such as DPP3, and as a selective antagonist of the P2RX3 receptor which is involved in pain signaling, these properties implicate it as a regulator of pain and inflammation.FUNCTION: Transcriptional activator which is required for calcium-dependent dendritic growth and branching in cortical neurons. Recruits CREB-binding protein (CREBBP) to nuclear bodies. Component of the CREST-BRG1 complex, a multiprotein complex that regulates promoter activation by orchestrating a calcium-dependent release of a repressor complex and a recruitment of an activator complex. In resting neurons, transcription of the c-FOS promoter is inhibited by BRG1-dependent recruitment of a phospho-RB1-HDAC1 repressor complex. Upon calcium influx, RB1 is dephosphorylated by calcineurin, which leads to release of the repressor complex. At the same time, there is increased recruitment of CREBBP to the promoter by a CREST-dependent mechanism, which leads to transcriptional activation. The CREST-BRG1 complex also binds to the NR2B promoter, and activity-dependent induction of NR2B expression involves a release of HDAC1 and recruitment of CREBBP (By similarity). {ECO:0000250}.

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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Fusion Gene Sequence for HBB-RPL3


check button For in-frame fusion transcripts, we provide the fusion transcript sequences and fusion amino acid sequences. To have fusion amino acid sequence, we ran ORFfinder and chose the longest ORF among the all predicted ones.

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Fusion Gene PPI Analysis for HBB-RPL3


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


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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Related Drugs for HBB-RPL3


check button Drugs targeting genes involved in this fusion gene.
(DrugBank Version 5.1.8 2021-05-08)
PartnerGeneUniProtAccDrugBank IDDrug nameDrug activityDrug typeDrug status
HgeneHBBP68871DB06154Pentaerythritol tetranitrateAgonistSmall moleculeApproved
HgeneHBBP68871DB09517Sodium ferric gluconate complexBindingSmall moleculeApproved
HgeneHBBP68871DB14548Zinc sulfate, unspecified formInducerSmall moleculeApproved|Experimental
HgeneHBBP68871DB01593ZincSmall moleculeApproved|Investigational
HgeneHBBP68871DB09112Nitrous acidOxidizerSmall moleculeApproved|Investigational
HgeneHBBP68871DB09130CopperSmall moleculeApproved|Investigational
HgeneHBBP68871DB13995Ferric pyrophosphate citrateBinderSmall moleculeApproved|Investigational
HgeneHBBP68871DB14487Zinc acetateSmall moleculeApproved|Investigational
HgeneHBBP68871DB14533Zinc chlorideInducerSmall moleculeApproved|Investigational
HgeneHBBP68871DB00893Iron DextranActivatorSmall moleculeApproved|Vet_approved

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Related Diseases for HBB-RPL3


check button Diseases associated with fusion partners.
(DisGeNet 4.0)
PartnerGeneDisease IDDisease name# pubmedsSource
HgeneHBBC0005283beta Thalassemia13CTD_human;GENOMICS_ENGLAND;UNIPROT
HgeneHBBC0002895Anemia, Sickle Cell8CTD_human;GENOMICS_ENGLAND;ORPHANET;UNIPROT
HgeneHBBC0002875Cooley's anemia7CTD_human;ORPHANET
HgeneHBBC0019025Hemoglobin F Disease7CTD_human;ORPHANET
HgeneHBBC0085578Thalassemia Minor6CTD_human
HgeneHBBC0271979Thalassemia Intermedia6CTD_human
HgeneHBBC0032461Polycythemia2CTD_human
HgeneHBBC0272080Hemoglobin D disease2ORPHANET
HgeneHBBC1527405Erythrocytosis2CTD_human
HgeneHBBC1858990Beta Thalassemia, Dominant Inclusion Body Type2CTD_human;GENOMICS_ENGLAND;ORPHANET
HgeneHBBC0010520Cyanosis1CTD_human
HgeneHBBC0013502Echinococcosis1CTD_human
HgeneHBBC0019021Hemoglobin C Disease1ORPHANET
HgeneHBBC0019045Hemoglobinopathies1CTD_human
HgeneHBBC0024535Malaria, Falciparum1CTD_human
HgeneHBBC0025637Methemoglobinemia1CTD_human
HgeneHBBC0032463Polycythemia Vera1CTD_human
HgeneHBBC0038002Splenomegaly1CTD_human
HgeneHBBC0238159Hemoglobin E disease1ORPHANET
HgeneHBBC0263454Chloracne1CTD_human
HgeneHBBC0271985Delta-Beta Thalassemia1ORPHANET
HgeneHBBC0472767Beta thalassemia intermedia1ORPHANET
HgeneHBBC0472777Hemoglobin E/beta thalassemia disease1ORPHANET
HgeneHBBC0700299Heinz Body Anemias1CTD_human;GENOMICS_ENGLAND
HgeneHBBC1841621FETAL HEMOGLOBIN QUANTITATIVE TRAIT LOCUS 11GENOMICS_ENGLAND
HgeneHBBC3665425Hemoglobin M Disease1ORPHANET
HgeneHBBC4551637Erythrocytosis familial, 11GENOMICS_ENGLAND
HgeneHBBC4553297Cystic Echinocccosis1CTD_human
TgeneC0007097Carcinoma1CTD_human
TgeneC0024667Animal Mammary Neoplasms1CTD_human
TgeneC0024668Mammary Neoplasms, Experimental1CTD_human
TgeneC0205696Anaplastic carcinoma1CTD_human
TgeneC0205697Carcinoma, Spindle-Cell1CTD_human
TgeneC0205698Undifferentiated carcinoma1CTD_human
TgeneC0205699Carcinomatosis1CTD_human
TgeneC1257925Mammary Carcinoma, Animal1CTD_human