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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:RSBN1-PTPN22 (FusionGDB2 ID:77906)

Fusion Gene Summary for RSBN1-PTPN22

check button Fusion gene summary
Fusion gene informationFusion gene name: RSBN1-PTPN22
Fusion gene ID: 77906
HgeneTgene
Gene symbol

RSBN1

PTPN22

Gene ID

54665

26191

Gene nameround spermatid basic protein 1protein tyrosine phosphatase non-receptor type 22
SynonymsKDM9|ROSBINLYP|LYP1|LYP2|PEP|PTPN22.5|PTPN22.6|PTPN8
Cytomap

1p13.2

1p13.2

Type of geneprotein-codingprotein-coding
Descriptionlysine-specific demethylase 9tyrosine-protein phosphatase non-receptor type 22PEST-domain phosphatasehematopoietic cell protein-tyrosine phosphatase 70Z-PEPlymphoid-specific protein tyrosine phosphataseprotein tyrosine phosphatase, non-receptor type 22 (lymphoid)protein tyrosine
Modification date2020031320200327
UniProtAcc..
Ensembl transtripts involved in fusion geneENST00000261441, ENST00000369581, 
ENST00000460620, ENST00000359785, 
ENST00000528414, ENST00000538253, 
ENST00000420377, ENST00000525799, 
ENST00000534519, 
Fusion gene scores* DoF score3 X 3 X 2=182 X 1 X 1=2
# samples 31
** MAII scorelog2(3/18*10)=0.736965594166206
effective Gene in Pan-Cancer Fusion Genes (eGinPCFGs).
DoF>8 and MAII>0
log2(1/2*10)=2.32192809488736
Context

PubMed: RSBN1 [Title/Abstract] AND PTPN22 [Title/Abstract] AND fusion [Title/Abstract]

Most frequent breakpointRSBN1(114354332)-PTPN22(114362276), # samples:2
Anticipated loss of major functional domain due to fusion event.RSBN1-PTPN22 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
TgenePTPN22

GO:0006470

protein dephosphorylation

10068674

TgenePTPN22

GO:0032817

regulation of natural killer cell proliferation

20522204

TgenePTPN22

GO:0050860

negative regulation of T cell receptor signaling pathway

18056643

TgenePTPN22

GO:0071225

cellular response to muramyl dipeptide

23991106


check buttonFusion gene breakpoints across RSBN1 (5'-gene)
* Click on the image to open the UCSC genome browser with custom track showing this image in a new window.

check buttonFusion gene breakpoints across PTPN22 (3'-gene)
* Click on the image to open the UCSC genome browser with custom track showing this image in a new window.

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
ChimerDB4CESCTCGA-C5-A3HD-01BRSBN1chr1

114354332

-PTPN22chr1

114362276

-
ChimerDB4CESCTCGA-C5-A3HD-01BRSBN1chr1

114354332

-PTPN22chr1

114362276

-


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Fusion Gene ORF analysis for RSBN1-PTPN22

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-shiftENST00000261441ENST00000460620RSBN1chr1

114354332

-PTPN22chr1

114362276

-
Frame-shiftENST00000261441ENST00000359785RSBN1chr1

114354332

-PTPN22chr1

114362276

-
Frame-shiftENST00000261441ENST00000528414RSBN1chr1

114354332

-PTPN22chr1

114362276

-
Frame-shiftENST00000261441ENST00000538253RSBN1chr1

114354332

-PTPN22chr1

114362276

-
Frame-shiftENST00000261441ENST00000420377RSBN1chr1

114354332

-PTPN22chr1

114362276

-
Frame-shiftENST00000261441ENST00000525799RSBN1chr1

114354332

-PTPN22chr1

114362276

-
5CDS-intronENST00000261441ENST00000534519RSBN1chr1

114354332

-PTPN22chr1

114362276

-
intron-3CDSENST00000369581ENST00000460620RSBN1chr1

114354332

-PTPN22chr1

114362276

-
intron-3CDSENST00000369581ENST00000359785RSBN1chr1

114354332

-PTPN22chr1

114362276

-
intron-3CDSENST00000369581ENST00000528414RSBN1chr1

114354332

-PTPN22chr1

114362276

-
intron-3CDSENST00000369581ENST00000538253RSBN1chr1

114354332

-PTPN22chr1

114362276

-
intron-3CDSENST00000369581ENST00000420377RSBN1chr1

114354332

-PTPN22chr1

114362276

-
intron-3CDSENST00000369581ENST00000525799RSBN1chr1

114354332

-PTPN22chr1

114362276

-
intron-intronENST00000369581ENST00000534519RSBN1chr1

114354332

-PTPN22chr1

114362276

-

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 RSBN1-PTPN22


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.

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 RSBN1-PTPN22


check button Go to

FGviewer for the breakpoints of :-:

.
- FGviewer provides the online visualization of the retention search of the protein functional features across DNA, RNA, protein, and pathological levels.
FGviewer

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

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 RSBN1-PTPN22


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 RSBN1-PTPN22


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 RSBN1-PTPN22


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 RSBN1-PTPN22


check button Diseases associated with fusion partners.
(DisGeNet 4.0)
PartnerGeneDisease IDDisease name# pubmedsSource
TgenePTPN22C0024141Lupus Erythematosus, Systemic8CTD_human;ORPHANET;UNIPROT
TgenePTPN22C0003873Rheumatoid Arthritis6CTD_human;UNIPROT
TgenePTPN22C0011854Diabetes Mellitus, Insulin-Dependent3CTD_human;UNIPROT
TgenePTPN22C0205734Diabetes, Autoimmune2CTD_human
TgenePTPN22C0242380Libman-Sacks Disease2CTD_human
TgenePTPN22C0342302Brittle diabetes2CTD_human
TgenePTPN22C3495801Granulomatosis with polyangiitis2ORPHANET
TgenePTPN22C3837958Diabetes Mellitus, Ketosis-Prone2CTD_human
TgenePTPN22C4554117Diabetes Mellitus, Sudden-Onset2CTD_human
TgenePTPN22C0004364Autoimmune Diseases1CTD_human
TgenePTPN22C0018213Graves Disease1CTD_human
TgenePTPN22C0021390Inflammatory Bowel Diseases1CTD_human
TgenePTPN22C0039483Giant Cell Arteritis1ORPHANET
TgenePTPN22C0042170Uveomeningoencephalitic Syndrome1ORPHANET
TgenePTPN22C1956391Temporal Arteritis1ORPHANET
TgenePTPN22C2931171Juvenile pauciarticular chronic arthritis1ORPHANET
TgenePTPN22C3277701VITILIGO-ASSOCIATED MULTIPLE AUTOIMMUNE DISEASE SUSCEPTIBILITY 61UNIPROT