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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:RPN2-MYL9

Fusion Protein Summary

check button Fusion gene summary
Fusion partner gene informationFusion gene name: RPN2-MYL9
FusionPDB ID: 77200
FusionGDB2.0 ID: 77200
HgeneTgene
Gene symbol

RPN2

MYL9

Gene ID

6185

10398

Gene nameribophorin IImyosin light chain 9
SynonymsRIBIIR|RPN-II|RPNII|SWP1LC20|MLC-2C|MLC2|MRLC1|MYRL2
Cytomap

20q11.23

20q11.23

Type of geneprotein-codingprotein-coding
Descriptiondolichyl-diphosphooligosaccharide--protein glycosyltransferase subunit 2dolichyl-diphosphooligosaccharide--protein glycosyltransferase 63 kDa subunitoligosaccharyltransferase complex subunit (non-catalytic)ribophorin-2myosin regulatory light polypeptide 920 kDa myosin light chainepididymis secretory sperm binding proteinmyosin RLCmyosin regulatory light chain 1myosin regulatory light chain 2, smooth muscle isoformmyosin regulatory light chain 9myosin regulatory
Modification date2020031320200313
UniProtAcc.

P24844

Ensembl transtripts involved in fusion geneENST idsENST00000237530, ENST00000373622, 
ENST00000470352, 
ENST00000279022, 
ENST00000346786, 
Fusion gene scores for assessment (based on all fusion genes of FusionGDB 2.0)* DoF score15 X 12 X 8=14405 X 4 X 4=80
# samples 175
** MAII scorelog2(17/1440*10)=-3.08246216019197
possibly effective Gene in Pan-Cancer Fusion Genes (peGinPCFGs).
DoF>8 and MAII<0
log2(5/80*10)=-0.678071905112638
possibly effective Gene in Pan-Cancer Fusion Genes (peGinPCFGs).
DoF>8 and MAII<0
Context (manual curation of fusion genes in FusionPDB)

PubMed: RPN2 [Title/Abstract] AND MYL9 [Title/Abstract] AND fusion [Title/Abstract]

Most frequent breakpoint (based on all fusion genes of FusionGDB 2.0)RPN2(35842268)-MYL9(35177480), # samples:2
Anticipated loss of major functional domain due to fusion event.RPN2-MYL9 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.
RPN2-MYL9 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.
RPN2-MYL9 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.
RPN2-MYL9 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 RPN2 (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 MYL9 (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
ChimerDB4LUSCTCGA-66-2793-01ARPN2chr20

35842268

+MYL9chr20

35177480

+
ChimerDB4LUSCTCGA-66-2793RPN2chr20

35842268

+MYL9chr20

35177480

+


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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)
ENST00000237530RPN2chr2035842268+ENST00000279022MYL9chr2035177480+215214032091744511
ENST00000237530RPN2chr2035842268+ENST00000346786MYL9chr2035177480+215214032091744511
ENST00000373622RPN2chr2035842268+ENST00000279022MYL9chr2035177480+19411192941533479
ENST00000373622RPN2chr2035842268+ENST00000346786MYL9chr2035177480+19411192941533479

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
ENST00000237530ENST00000279022RPN2chr2035842268+MYL9chr2035177480+0.0156533510.9843466
ENST00000237530ENST00000346786RPN2chr2035842268+MYL9chr2035177480+0.0156533510.9843466
ENST00000373622ENST00000279022RPN2chr2035842268+MYL9chr2035177480+0.0151579950.98484194
ENST00000373622ENST00000346786RPN2chr2035842268+MYL9chr2035177480+0.0151579950.98484194

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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

>77200_77200_1_RPN2-MYL9_RPN2_chr20_35842268_ENST00000237530_MYL9_chr20_35177480_ENST00000279022_length(amino acids)=511AA_BP=398
MPRVPGVPCGGLLEPLSRAEVSPRLGLRRDLLGGMAPPGSSTVFLLALTIIASTWALTPTHYLTKHDVERLKASLDRPFTNLESAFYSIV
GLSSLGAQVPDAKKACTYIRSNLDPSNVDSLFYAAQASQALSGCEISISNETKDLLLAAVSEDSSVTQIYHAVAALSGFGLPLASQEALS
ALTARLSKEETVLATVQALQTASHLSQQADLRSIVEEIEDLVARLDELGGVYLQFEEGLETTALFVAATYKLMDHVGTEPSIKEDQVIQL
MNAIFSKKNFESLSEAFSVASAAAVLSHNRYHVPVVVVPEGSASDTHEQAILRLQVTNVLSQPLTQATVKLEHAKSVASRATVLQKTSFT
PVGDVFELNFMNVKFSSGYYDFLVEVEGDNRYIANTVEVSSMRTTSGSCSPPWVTASQMRKWTRCTGRHPLIRKATSTTWSSPASSNMAP

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

>77200_77200_2_RPN2-MYL9_RPN2_chr20_35842268_ENST00000237530_MYL9_chr20_35177480_ENST00000346786_length(amino acids)=511AA_BP=398
MPRVPGVPCGGLLEPLSRAEVSPRLGLRRDLLGGMAPPGSSTVFLLALTIIASTWALTPTHYLTKHDVERLKASLDRPFTNLESAFYSIV
GLSSLGAQVPDAKKACTYIRSNLDPSNVDSLFYAAQASQALSGCEISISNETKDLLLAAVSEDSSVTQIYHAVAALSGFGLPLASQEALS
ALTARLSKEETVLATVQALQTASHLSQQADLRSIVEEIEDLVARLDELGGVYLQFEEGLETTALFVAATYKLMDHVGTEPSIKEDQVIQL
MNAIFSKKNFESLSEAFSVASAAAVLSHNRYHVPVVVVPEGSASDTHEQAILRLQVTNVLSQPLTQATVKLEHAKSVASRATVLQKTSFT
PVGDVFELNFMNVKFSSGYYDFLVEVEGDNRYIANTVEVSSMRTTSGSCSPPWVTASQMRKWTRCTGRHPLIRKATSTTWSSPASSNMAP

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

>77200_77200_3_RPN2-MYL9_RPN2_chr20_35842268_ENST00000373622_MYL9_chr20_35177480_ENST00000279022_length(amino acids)=479AA_BP=366
MPRVPGVPCGGLLEPLSRAEVSPRLGLRRDLLGGMAPPGSSTVFLLALTIIASTWALTPTHYLTKHDVERLKASLDRPFTNLESAFYSIV
GLSSLGAQVPDAKISISNETKDLLLAAVSEDSSVTQIYHAVAALSGFGLPLASQEALSALTARLSKEETVLATVQALQTASHLSQQADLR
SIVEEIEDLVARLDELGGVYLQFEEGLETTALFVAATYKLMDHVGTEPSIKEDQVIQLMNAIFSKKNFESLSEAFSVASAAAVLSHNRYH
VPVVVVPEGSASDTHEQAILRLQVTNVLSQPLTQATVKLEHAKSVASRATVLQKTSFTPVGDVFELNFMNVKFSSGYYDFLVEVEGDNRY
IANTVEVSSMRTTSGSCSPPWVTASQMRKWTRCTGRHPLIRKATSTTWSSPASSNMAPRIKTTRPPQPPDTPAPASHPSPHTPVHTSSLP

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

>77200_77200_4_RPN2-MYL9_RPN2_chr20_35842268_ENST00000373622_MYL9_chr20_35177480_ENST00000346786_length(amino acids)=479AA_BP=366
MPRVPGVPCGGLLEPLSRAEVSPRLGLRRDLLGGMAPPGSSTVFLLALTIIASTWALTPTHYLTKHDVERLKASLDRPFTNLESAFYSIV
GLSSLGAQVPDAKISISNETKDLLLAAVSEDSSVTQIYHAVAALSGFGLPLASQEALSALTARLSKEETVLATVQALQTASHLSQQADLR
SIVEEIEDLVARLDELGGVYLQFEEGLETTALFVAATYKLMDHVGTEPSIKEDQVIQLMNAIFSKKNFESLSEAFSVASAAAVLSHNRYH
VPVVVVPEGSASDTHEQAILRLQVTNVLSQPLTQATVKLEHAKSVASRATVLQKTSFTPVGDVFELNFMNVKFSSGYYDFLVEVEGDNRY
IANTVEVSSMRTTSGSCSPPWVTASQMRKWTRCTGRHPLIRKATSTTWSSPASSNMAPRIKTTRPPQPPDTPAPASHPSPHTPVHTSSLP

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

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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/chr20:35842268/chr20:35177480)
- 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
.MYL9

P24844

FUNCTION: Might normally function as a transcriptional repressor. EWS-fusion-proteins (EFPS) may play a role in the tumorigenic process. They may disturb gene expression by mimicking, or interfering with the normal function of CTD-POLII within the transcription initiation complex. They may also contribute to an aberrant activation of the fusion protein target genes.FUNCTION: Myosin regulatory subunit that plays an important role in regulation of both smooth muscle and nonmuscle cell contractile activity via its phosphorylation. Implicated in cytokinesis, receptor capping, and cell locomotion (PubMed:11942626, PubMed:2526655). In myoblasts, may regulate PIEZO1-dependent cortical actomyosin assembly involved in myotube formation (By similarity). {ECO:0000250|UniProtKB:Q9CQ19, ECO:0000269|PubMed:11942626, ECO:0000269|PubMed:2526655}.

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
TgeneMYL9chr20:35842268chr20:35177480ENST0000027902224134_169115.33333333333333173.0DomainEF-hand 3
TgeneMYL9chr20:35842268chr20:35177480ENST0000034678613134_16961.333333333333336119.0DomainEF-hand 3
TgeneMYL9chr20:35842268chr20:35177480ENST000003467861398_13361.333333333333336119.0DomainEF-hand 2

- Not-retained protein feature among the 13 regional features.
PartnerGeneHbpTbpENSTStrandBPexonTotalExonProtein feature loci*BPlociTotalLenProtein featureProtein feature note
HgeneRPN2chr20:35842268chr20:35177480ENST00000237530+91723_540364.0632.0Topological domainLumenal
HgeneRPN2chr20:35842268chr20:35177480ENST00000237530+917562_571364.0632.0Topological domainCytoplasmic
HgeneRPN2chr20:35842268chr20:35177480ENST00000237530+917593_596364.0632.0Topological domainLumenal
HgeneRPN2chr20:35842268chr20:35177480ENST00000237530+917618_631364.0632.0Topological domainCytoplasmic
HgeneRPN2chr20:35842268chr20:35177480ENST00000373622+81723_540332.0616.0Topological domainLumenal
HgeneRPN2chr20:35842268chr20:35177480ENST00000373622+817562_571332.0616.0Topological domainCytoplasmic
HgeneRPN2chr20:35842268chr20:35177480ENST00000373622+817593_596332.0616.0Topological domainLumenal
HgeneRPN2chr20:35842268chr20:35177480ENST00000373622+817618_631332.0616.0Topological domainCytoplasmic
HgeneRPN2chr20:35842268chr20:35177480ENST00000237530+917541_561364.0632.0TransmembraneHelical
HgeneRPN2chr20:35842268chr20:35177480ENST00000237530+917572_592364.0632.0TransmembraneHelical
HgeneRPN2chr20:35842268chr20:35177480ENST00000237530+917597_617364.0632.0TransmembraneHelical
HgeneRPN2chr20:35842268chr20:35177480ENST00000373622+817541_561332.0616.0TransmembraneHelical
HgeneRPN2chr20:35842268chr20:35177480ENST00000373622+817572_592332.0616.0TransmembraneHelical
HgeneRPN2chr20:35842268chr20:35177480ENST00000373622+817597_617332.0616.0TransmembraneHelical
TgeneMYL9chr20:35842268chr20:35177480ENST000002790222442_53115.33333333333333173.0Calcium binding.
TgeneMYL9chr20:35842268chr20:35177480ENST000003467861342_5361.333333333333336119.0Calcium binding.
TgeneMYL9chr20:35842268chr20:35177480ENST000002790222429_64115.33333333333333173.0DomainEF-hand 1
TgeneMYL9chr20:35842268chr20:35177480ENST000002790222498_133115.33333333333333173.0DomainEF-hand 2
TgeneMYL9chr20:35842268chr20:35177480ENST000003467861329_6461.333333333333336119.0DomainEF-hand 1


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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 >>>1087_RPN2_35842268_MYL9_35177480_1087_RPN2_35842268_MYL9_35177480_ranked_0.pdbRPN23584226835842268ENST00000346786MYL9chr2035177480+
MPRVPGVPCGGLLEPLSRAEVSPRLGLRRDLLGGMAPPGSSTVFLLALTIIASTWALTPTHYLTKHDVERLKASLDRPFTNLESAFYSIV
GLSSLGAQVPDAKKACTYIRSNLDPSNVDSLFYAAQASQALSGCEISISNETKDLLLAAVSEDSSVTQIYHAVAALSGFGLPLASQEALS
ALTARLSKEETVLATVQALQTASHLSQQADLRSIVEEIEDLVARLDELGGVYLQFEEGLETTALFVAATYKLMDHVGTEPSIKEDQVIQL
MNAIFSKKNFESLSEAFSVASAAAVLSHNRYHVPVVVVPEGSASDTHEQAILRLQVTNVLSQPLTQATVKLEHAKSVASRATVLQKTSFT
PVGDVFELNFMNVKFSSGYYDFLVEVEGDNRYIANTVEVSSMRTTSGSCSPPWVTASQMRKWTRCTGRHPLIRKATSTTWSSPASSNMAP
511


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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.
RPN2_pLDDT.png
all structure
all structure
MYL9_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
RPN2
MYL9


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 RPN2-MYL9


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 RPN2-MYL9


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