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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:RPN1-SLC22A13 (FusionGDB2 ID:77190)

Fusion Gene Summary for RPN1-SLC22A13

check button Fusion gene summary
Fusion gene informationFusion gene name: RPN1-SLC22A13
Fusion gene ID: 77190
HgeneTgene
Gene symbol

RPN1

SLC22A13

Gene ID

6184

9390

Gene nameribophorin Isolute carrier family 22 member 13
SynonymsOST1|RBPH1OAT10|OCTL1|OCTL3|ORCTL-3|ORCTL3
Cytomap

3q21.3

3p22.2

Type of geneprotein-codingprotein-coding
Descriptiondolichyl-diphosphooligosaccharide--protein glycosyltransferase subunit 1RPN-Idolichyl-diphosphooligosaccharide-protein glycosyltransferase 67 kDa subunitoligosaccharyltransferase 1 homologoligosaccharyltransferase complex subunit (non-catalytic)ribopsolute carrier family 22 member 13organic cationic transporter-like 3organic-cation transporter like 3solute carrier family 22 (organic anion transporter), member 13solute carrier family 22 (organic anion/urate transporter), member 13
Modification date2020032720200313
UniProtAcc..
Ensembl transtripts involved in fusion geneENST00000296255, ENST00000497289, 
ENST00000490166, 
ENST00000311856, 
ENST00000450935, 
Fusion gene scores* DoF score8 X 10 X 8=6401 X 1 X 1=1
# samples 101
** MAII scorelog2(10/640*10)=-2.67807190511264
possibly effective Gene in Pan-Cancer Fusion Genes (peGinPCFGs).
DoF>8 and MAII<0
log2(1/1*10)=3.32192809488736
Context

PubMed: RPN1 [Title/Abstract] AND SLC22A13 [Title/Abstract] AND fusion [Title/Abstract]

Most frequent breakpointRPN1(128348794)-SLC22A13(38307485), # samples:2
Anticipated loss of major functional domain due to fusion event.RPN1-SLC22A13 seems lost the major protein functional domain in Hgene partner, which is a cell metabolism gene due to the frame-shifted ORF.
RPN1-SLC22A13 seems lost the major protein functional domain in Hgene partner, which is a CGC due to the frame-shifted ORF.
RPN1-SLC22A13 seems lost the major protein functional domain in Hgene partner, which is a essential gene due to the frame-shifted ORF.
RPN1-SLC22A13 seems lost the major protein functional domain in Tgene partner, which is a essential gene due to the frame-shifted ORF.
RPN1-SLC22A13 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
TgeneSLC22A13

GO:0015747

urate transport

10072596

TgeneSLC22A13

GO:2001142

nicotinate transport

18411268


check buttonFusion gene breakpoints across RPN1 (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 SLC22A13 (3'-gene)
* Click on the image to open the UCSC genome browser with custom track showing this image in a new window.
all structure

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
ChimerDB4SKCMTCGA-W3-AA1R-06ARPN1chr3

128348794

-SLC22A13chr3

38307485

+


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Fusion Gene ORF analysis for RPN1-SLC22A13

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-shiftENST00000296255ENST00000311856RPN1chr3

128348794

-SLC22A13chr3

38307485

+
Frame-shiftENST00000296255ENST00000450935RPN1chr3

128348794

-SLC22A13chr3

38307485

+
Frame-shiftENST00000497289ENST00000311856RPN1chr3

128348794

-SLC22A13chr3

38307485

+
In-frameENST00000497289ENST00000450935RPN1chr3

128348794

-SLC22A13chr3

38307485

+
intron-3CDSENST00000490166ENST00000311856RPN1chr3

128348794

-SLC22A13chr3

38307485

+
intron-3CDSENST00000490166ENST00000450935RPN1chr3

128348794

-SLC22A13chr3

38307485

+

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)
ENST00000497289RPN1chr3128348794-ENST00000450935SLC22A13chr338307485+208710972261128300

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
ENST00000497289ENST00000450935RPN1chr3128348794-SLC22A13chr338307485+0.0062804130.9937196

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Fusion Genomic Features for RPN1-SLC22A13


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)

check buttonDistribution of 44 human genomic features loci across 20kb length fusion breakpoint regions. We integrated a total of 44 different types of human genomic feature loci information across five big categories including virus integration sites, repeats, structural variants, chromatin states, and gene expression regulation. More details are in help page.
genomic feature

check buttonDistribution of 44 human genomic features loci across 20kb length fusion breakpoint regions that are ovelapped with the top 1% feature importance score regions. More details are in help page.

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Fusion Protein Features for RPN1-SLC22A13


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/chr3:128348794/chr3:38307485)
- 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
..
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}.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
TgeneSLC22A13chr3:128348794chr3:38307485ENST00000311856010160_1670552.0Topological domainCytoplasmic
TgeneSLC22A13chr3:128348794chr3:38307485ENST00000311856010189_1950552.0Topological domainExtracellular
TgeneSLC22A13chr3:128348794chr3:38307485ENST000003118560101_200552.0Topological domainCytoplasmic
TgeneSLC22A13chr3:128348794chr3:38307485ENST00000311856010217_2240552.0Topological domainCytoplasmic
TgeneSLC22A13chr3:128348794chr3:38307485ENST00000311856010246_2510552.0Topological domainExtracellular
TgeneSLC22A13chr3:128348794chr3:38307485ENST00000311856010273_3320552.0Topological domainCytoplasmic
TgeneSLC22A13chr3:128348794chr3:38307485ENST00000311856010354_3540552.0Topological domainExtracellular
TgeneSLC22A13chr3:128348794chr3:38307485ENST00000311856010376_3970552.0Topological domainCytoplasmic
TgeneSLC22A13chr3:128348794chr3:38307485ENST00000311856010419_4270552.0Topological domainExtracellular
TgeneSLC22A13chr3:128348794chr3:38307485ENST0000031185601042_1380552.0Topological domainExtracellular
TgeneSLC22A13chr3:128348794chr3:38307485ENST00000311856010449_4520552.0Topological domainCytoplasmic
TgeneSLC22A13chr3:128348794chr3:38307485ENST00000311856010474_4780552.0Topological domainExtracellular
TgeneSLC22A13chr3:128348794chr3:38307485ENST00000311856010500_5510552.0Topological domainCytoplasmic
TgeneSLC22A13chr3:128348794chr3:38307485ENST00000311856010139_1590552.0TransmembraneHelical
TgeneSLC22A13chr3:128348794chr3:38307485ENST00000311856010168_1880552.0TransmembraneHelical
TgeneSLC22A13chr3:128348794chr3:38307485ENST00000311856010196_2160552.0TransmembraneHelical
TgeneSLC22A13chr3:128348794chr3:38307485ENST0000031185601021_410552.0TransmembraneHelical
TgeneSLC22A13chr3:128348794chr3:38307485ENST00000311856010225_2450552.0TransmembraneHelical
TgeneSLC22A13chr3:128348794chr3:38307485ENST00000311856010252_2720552.0TransmembraneHelical
TgeneSLC22A13chr3:128348794chr3:38307485ENST00000311856010333_3530552.0TransmembraneHelical
TgeneSLC22A13chr3:128348794chr3:38307485ENST00000311856010355_3750552.0TransmembraneHelical
TgeneSLC22A13chr3:128348794chr3:38307485ENST00000311856010398_4180552.0TransmembraneHelical
TgeneSLC22A13chr3:128348794chr3:38307485ENST00000311856010428_4480552.0TransmembraneHelical
TgeneSLC22A13chr3:128348794chr3:38307485ENST00000311856010453_4730552.0TransmembraneHelical
TgeneSLC22A13chr3:128348794chr3:38307485ENST00000311856010479_4990552.0TransmembraneHelical

- In-frame and not-retained protein feature among the 13 regional features.
PartnerGeneHbpTbpENSTStrandBPexonTotalExonProtein feature loci*BPlociTotalLenProtein featureProtein feature note
HgeneRPN1chr3:128348794chr3:38307485ENST00000296255-51024_438345608.0Topological domainLumenal
HgeneRPN1chr3:128348794chr3:38307485ENST00000296255-510458_607345608.0Topological domainCytoplasmic
HgeneRPN1chr3:128348794chr3:38307485ENST00000296255-510439_457345608.0TransmembraneHelical


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Fusion Gene Sequence for RPN1-SLC22A13


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.
>77190_77190_1_RPN1-SLC22A13_RPN1_chr3_128348794_ENST00000497289_SLC22A13_chr3_38307485_ENST00000450935_length(transcript)=2087nt_BP=1097nt
CATCTTTTACAAGAAACCTTCGCTGCAACCGCTGCGTCACATCACCGCGTCTCCCAGGGACAGGAAAGCCTCTCCGTGTTTGGTGAAGCT
TCAGGGGAAGCAGTCATCCTGTCGTCGCATACGGCAAAATCCTCCATTGCCGTAGCCGTTCGGCTGACGTGACAAGGGAGGTGCAGGCCA
ACACGGCGACTCCGCGCCCTCTGGCGGCAGTGCCGGAGCAGCGGCGCTGTCTTTGACCTATCCGGCATTCGGCTTCCGGGACCGCTTGGC
GGCTGTGAATGCAGAGCTGGGGCGACGTGGGGCTCGCTTCCTGGGACTGGGTGTAAAGGGAGAAGATGAGGAAGAGAACAATTTGGAAGT
ACGTGAAACCAAAATTAAGGGTAAAAGTGGGAGATTCTTCACAGTCAAGCTCCCAGTTGCTCTTGATCCTGGGGCCAAGATTTCAGTCAT
TGTGGAAACAGTCTACACCCATGTGCTTCATCCGTATCCAACCCAGATCACCCAGTCAGAGAAACAGTTTGTGGTGTTTGAGGGGAACCA
TTATTTCTACTCTCCCTATCCAACGAAGACACAAACCATGCGTGTGAAGCTTGCCTCTCGAAATGTGGAGAGCTACACCAAGCTGGGGAA
CCCCACGCGCTCTGAGGACCTACTGGATTATGGGCCTTTCAGAGATGTGCCTGCCTATAGTCAGGATACTTTTAAAGTACATTATGAGAA
CAACAGCCCTTTCCTGACCATCACCAGCATGACCCGAGTCATTGAAGTCTCTCACTGGGGTAATATTGCTGTGGAAGAAAATGTGGACTT
AAAGCACACAGGAGCTGTGCTTAAGGGGCCTTTCTCACGCTATGATTACCAGAGACAGCCAGATAGTGGAATATCCTCCATCCGTTCTTT
TAAGACCATCCTTCCTGCTGCTGCCCAGGATGTTTATTACCGGGATGAGATTGGCAATGTTTCTACCAGCCACCTCCTTATTTTGGATGA
CTCTGTAGAGATGGAAATCCGGCCTCGCTTCCCTCTCTTTGGCGGGTGGAAGACCCATTACATCGTTGGCTACAACCTCCCAAGCTATGA
GTACCTCTATAATTTGGTGAGCCCCACCACTGTGCAGTGGCTTGGGTGAAGAACCACACTTTCAACCTGAGTGCTGCTGAACAGCTGGTA
CTGAGCGTGCCCCTGGACACTGCAGGTCACCCAGAGCCCTGCCTCATGTTCCGGCCACCCCCCGCCAATGCCAGCCTGCAGGACATCCTC
AGCCACCGCTTCAATGAGACGCAGCCTTGTGATATGGGCTGGGAATATCCTGAGAACAGGCTCCCATCCCTGAAGAATGAGTTCAACCTG
GTTTGTGATCGGAAGCACCTGAAGGACACCACACAGTCAGTGTTCATGGCTGGGCTCCTTGTTGGCACCCTCATGTTTGGGCCCCTCTGC
GACCGTGACAGAATGGGTGGGGCCCTCATGGAGGACGCAGGCCGTGGTCCTGGCCCAGTGCAACTTCTCCCTCGGGCAGATGGTGCTTGC
GGGACTCGCCTACGGTTTCCGCAACTGGAGGCTCCTTCAGATCACCGGCACTGCGCCTGGCTTACTGCTCTTCTTCTACTTCTGGGCTCT
GCCAGAATCTGCACGTTGGCTCCTGACCCGTGGGAGGATGGACGAGGCGATACAACTGATCCAGAAGGCGGCCTCGGTCAATAGGCGGAA
ACTCTCCCCGGAGCTCATGAACCAGCTGGTCCCAGAGAAGACAGGCCCCTCAGGGAATGCCCTGGATCTGTTCAGACACCCCCAGCTCCG
GAAGGTGACCCTGATTATCTTCTGTGTCTGGTTTGTGGACAGTCTGGGGTACTACGGCCTGAGCCTCCAAGTGGGGGACTTCGGCCTGGA
CGTCTATCTGACGCAGCTCATCTTTGGAGCTGTTGAGGTGCCTGCCCGCTGTTCCAGCATCTTCATGATGCAGAGGTTTGGCCGCAAGTG
GAGCCAGTTGGGGACCTTGGTCTTGGGTGGCCTGATGTGTATCATCATCATCTTCATCCCAGCAGATCTGCCCGTGGTGGTCACCATGCT

>77190_77190_1_RPN1-SLC22A13_RPN1_chr3_128348794_ENST00000497289_SLC22A13_chr3_38307485_ENST00000450935_length(amino acids)=300AA_BP=
MSLTYPAFGFRDRLAAVNAELGRRGARFLGLGVKGEDEEENNLEVRETKIKGKSGRFFTVKLPVALDPGAKISVIVETVYTHVLHPYPTQ
ITQSEKQFVVFEGNHYFYSPYPTKTQTMRVKLASRNVESYTKLGNPTRSEDLLDYGPFRDVPAYSQDTFKVHYENNSPFLTITSMTRVIE
VSHWGNIAVEENVDLKHTGAVLKGPFSRYDYQRQPDSGISSIRSFKTILPAAAQDVYYRDEIGNVSTSHLLILDDSVEMEIRPRFPLFGG

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

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Fusion Gene PPI Analysis for RPN1-SLC22A13


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 RPN1-SLC22A13


check button Drugs targeting genes involved in this fusion gene.
(DrugBank Version 5.1.8 2021-05-08)
PartnerGeneUniProtAccDrugBank IDDrug nameDrug activityDrug typeDrug status

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Related Diseases for RPN1-SLC22A13


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