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Center for Computational Systems Medicine level1
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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-Protein Interaction

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Related drugs with this fusion protein

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Related disease with this fusion protein

Fusion Protein:NNAT-PTPRN2

Fusion Protein Summary

check button Fusion gene summary
Fusion partner gene informationFusion gene name: NNAT-PTPRN2
FusionPDB ID: 59480
FusionGDB2.0 ID: 59480
HgeneTgene
Gene symbol

NNAT

PTPRN2

Gene ID

4826

5799

Gene nameneuronatinprotein tyrosine phosphatase receptor type N2
SynonymsPeg5IA-2beta|IAR|ICAAR|PTPRP|R-PTP-N2
Cytomap

20q11.23

7q36.3

Type of geneprotein-codingprotein-coding
Descriptionneuronatinreceptor-type tyrosine-protein phosphatase N2IAR/receptor-like protein-tyrosine phosphataseislet cell autoantigen-related proteinphogrinprotein tyrosine phosphatase receptor piprotein tyrosine phosphatase, receptor type, N polypeptide 2tyrosine phos
Modification date2020031320200313
UniProtAcc

Q16517

.
Ensembl transtripts involved in fusion geneENST idsENST00000062104, ENST00000346199, 
ENST00000389413, ENST00000389416, 
ENST00000389418, ENST00000404321, 
ENST00000409483, 
Fusion gene scores for assessment (based on all fusion genes of FusionGDB 2.0)* DoF score4 X 4 X 1=1616 X 17 X 9=2448
# samples 424
** MAII scorelog2(4/16*10)=1.32192809488736
effective Gene in Pan-Cancer Fusion Genes (eGinPCFGs).
DoF>8 and MAII>0
log2(24/2448*10)=-3.35049724708413
possibly effective Gene in Pan-Cancer Fusion Genes (peGinPCFGs).
DoF>8 and MAII<0
Context (manual curation of fusion genes in FusionPDB)

PubMed: NNAT [Title/Abstract] AND PTPRN2 [Title/Abstract] AND fusion [Title/Abstract]

Most frequent breakpoint (based on all fusion genes of FusionGDB 2.0)NNAT(36149805)-PTPRN2(157388013), # samples:1
Anticipated loss of major functional domain due to fusion event.NNAT-PTPRN2 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.
NNAT-PTPRN2 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.
NNAT-PTPRN2 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.
NNAT-PTPRN2 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 NNAT (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 PTPRN2 (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
ChiTaRS5.0N/ADA346166NNATchr20

36149805

+PTPRN2chr7

157388013

-


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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)
ENST00000062104NNATchr2036149805+ENST00000389413PTPRN2chr7157388013-2477189117818233
ENST00000062104NNATchr2036149805+ENST00000409483PTPRN2chr7157388013-2477189117818233
ENST00000062104NNATchr2036149805+ENST00000389416PTPRN2chr7157388013-2472189117818233
ENST00000062104NNATchr2036149805+ENST00000389418PTPRN2chr7157388013-2467189117818233
ENST00000062104NNATchr2036149805+ENST00000404321PTPRN2chr7157388013-819189117818233
ENST00000346199NNATchr2036149805+ENST00000389413PTPRN2chr7157388013-2473185113814233
ENST00000346199NNATchr2036149805+ENST00000409483PTPRN2chr7157388013-2473185113814233
ENST00000346199NNATchr2036149805+ENST00000389416PTPRN2chr7157388013-2468185113814233
ENST00000346199NNATchr2036149805+ENST00000389418PTPRN2chr7157388013-2463185113814233
ENST00000346199NNATchr2036149805+ENST00000404321PTPRN2chr7157388013-815185113814234

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
ENST00000062104ENST00000389413NNATchr2036149805+PTPRN2chr7157388013-0.0026675050.99733245
ENST00000062104ENST00000409483NNATchr2036149805+PTPRN2chr7157388013-0.0026675050.99733245
ENST00000062104ENST00000389416NNATchr2036149805+PTPRN2chr7157388013-0.0026009850.997399
ENST00000062104ENST00000389418NNATchr2036149805+PTPRN2chr7157388013-0.0026245760.9973755
ENST00000062104ENST00000404321NNATchr2036149805+PTPRN2chr7157388013-0.0034595320.9965405
ENST00000346199ENST00000389413NNATchr2036149805+PTPRN2chr7157388013-0.0020595780.99794036
ENST00000346199ENST00000409483NNATchr2036149805+PTPRN2chr7157388013-0.0020595780.99794036
ENST00000346199ENST00000389416NNATchr2036149805+PTPRN2chr7157388013-0.0020163820.9979836
ENST00000346199ENST00000389418NNATchr2036149805+PTPRN2chr7157388013-0.0020334580.9979665
ENST00000346199ENST00000404321NNATchr2036149805+PTPRN2chr7157388013-0.0033335440.9966665

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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

>59480_59480_1_NNAT-PTPRN2_NNAT_chr20_36149805_ENST00000062104_PTPRN2_chr7_157388013_ENST00000389413_length(amino acids)=233AA_BP=22
MAAVAAASAELLIIGWYIFRVLLQMDHDPRNPAYIATQGPLPATVADFWQMVWESGCVVIVMLTPLAENGVRQCYHYWPDEGSNLYHIYE
VNLVSEHIWCEDFLVRSFYLKNLQTNETRTVTQFHFLSWYDRGVPSSSRSLLDFRRKVNKCYRGRSCPIIVHCSDGAGRSGTYVLIDMVL

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

>59480_59480_2_NNAT-PTPRN2_NNAT_chr20_36149805_ENST00000062104_PTPRN2_chr7_157388013_ENST00000389416_length(amino acids)=233AA_BP=22
MAAVAAASAELLIIGWYIFRVLLQMDHDPRNPAYIATQGPLPATVADFWQMVWESGCVVIVMLTPLAENGVRQCYHYWPDEGSNLYHIYE
VNLVSEHIWCEDFLVRSFYLKNLQTNETRTVTQFHFLSWYDRGVPSSSRSLLDFRRKVNKCYRGRSCPIIVHCSDGAGRSGTYVLIDMVL

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

>59480_59480_3_NNAT-PTPRN2_NNAT_chr20_36149805_ENST00000062104_PTPRN2_chr7_157388013_ENST00000389418_length(amino acids)=233AA_BP=22
MAAVAAASAELLIIGWYIFRVLLQMDHDPRNPAYIATQGPLPATVADFWQMVWESGCVVIVMLTPLAENGVRQCYHYWPDEGSNLYHIYE
VNLVSEHIWCEDFLVRSFYLKNLQTNETRTVTQFHFLSWYDRGVPSSSRSLLDFRRKVNKCYRGRSCPIIVHCSDGAGRSGTYVLIDMVL

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

>59480_59480_4_NNAT-PTPRN2_NNAT_chr20_36149805_ENST00000062104_PTPRN2_chr7_157388013_ENST00000404321_length(amino acids)=233AA_BP=22
MAAVAAASAELLIIGWYIFRVLLQMDHDPRNPAYIATQGPLPATVADFWQMVWESGCVVIVMLTPLAENGVRQCYHYWPDEGSNLYHIYE
VNLVSEHIWCEDFLVRSFYLKNLQTNETRTVTQFHFLSWYDRGVPSSSRSLLDFRRKVNKCYRGRSCPIIVHCSDGAGRSGTYVLIDMVL

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

>59480_59480_5_NNAT-PTPRN2_NNAT_chr20_36149805_ENST00000062104_PTPRN2_chr7_157388013_ENST00000409483_length(amino acids)=233AA_BP=22
MAAVAAASAELLIIGWYIFRVLLQMDHDPRNPAYIATQGPLPATVADFWQMVWESGCVVIVMLTPLAENGVRQCYHYWPDEGSNLYHIYE
VNLVSEHIWCEDFLVRSFYLKNLQTNETRTVTQFHFLSWYDRGVPSSSRSLLDFRRKVNKCYRGRSCPIIVHCSDGAGRSGTYVLIDMVL

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

>59480_59480_6_NNAT-PTPRN2_NNAT_chr20_36149805_ENST00000346199_PTPRN2_chr7_157388013_ENST00000389413_length(amino acids)=233AA_BP=22
MAAVAAASAELLIIGWYIFRVLLQMDHDPRNPAYIATQGPLPATVADFWQMVWESGCVVIVMLTPLAENGVRQCYHYWPDEGSNLYHIYE
VNLVSEHIWCEDFLVRSFYLKNLQTNETRTVTQFHFLSWYDRGVPSSSRSLLDFRRKVNKCYRGRSCPIIVHCSDGAGRSGTYVLIDMVL

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

>59480_59480_7_NNAT-PTPRN2_NNAT_chr20_36149805_ENST00000346199_PTPRN2_chr7_157388013_ENST00000389416_length(amino acids)=233AA_BP=22
MAAVAAASAELLIIGWYIFRVLLQMDHDPRNPAYIATQGPLPATVADFWQMVWESGCVVIVMLTPLAENGVRQCYHYWPDEGSNLYHIYE
VNLVSEHIWCEDFLVRSFYLKNLQTNETRTVTQFHFLSWYDRGVPSSSRSLLDFRRKVNKCYRGRSCPIIVHCSDGAGRSGTYVLIDMVL

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

>59480_59480_8_NNAT-PTPRN2_NNAT_chr20_36149805_ENST00000346199_PTPRN2_chr7_157388013_ENST00000389418_length(amino acids)=233AA_BP=22
MAAVAAASAELLIIGWYIFRVLLQMDHDPRNPAYIATQGPLPATVADFWQMVWESGCVVIVMLTPLAENGVRQCYHYWPDEGSNLYHIYE
VNLVSEHIWCEDFLVRSFYLKNLQTNETRTVTQFHFLSWYDRGVPSSSRSLLDFRRKVNKCYRGRSCPIIVHCSDGAGRSGTYVLIDMVL

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

>59480_59480_9_NNAT-PTPRN2_NNAT_chr20_36149805_ENST00000346199_PTPRN2_chr7_157388013_ENST00000404321_length(amino acids)=234AA_BP=22
MAAVAAASAELLIIGWYIFRVLLQMDHDPRNPAYIATQGPLPATVADFWQMVWESGCVVIVMLTPLAENGVRQCYHYWPDEGSNLYHIYE
VNLVSEHIWCEDFLVRSFYLKNLQTNETRTVTQFHFLSWYDRGVPSSSRSLLDFRRKVNKCYRGRSCPIIVHCSDGAGRSGTYVLIDMVL

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

>59480_59480_10_NNAT-PTPRN2_NNAT_chr20_36149805_ENST00000346199_PTPRN2_chr7_157388013_ENST00000409483_length(amino acids)=233AA_BP=22
MAAVAAASAELLIIGWYIFRVLLQMDHDPRNPAYIATQGPLPATVADFWQMVWESGCVVIVMLTPLAENGVRQCYHYWPDEGSNLYHIYE
VNLVSEHIWCEDFLVRSFYLKNLQTNETRTVTQFHFLSWYDRGVPSSSRSLLDFRRKVNKCYRGRSCPIIVHCSDGAGRSGTYVLIDMVL

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

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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/chr20:36149805/chr7:157388013)
- 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
NNAT

Q16517

.
FUNCTION: May participate in the maintenance of segment identity in the hindbrain and pituitary development, and maturation or maintenance of the overall structure of the nervous system. May function as a regulatory subunit of ion channels.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.
- Retained protein feature among the 13 regional features.
PartnerGeneHbpTbpENSTStrandBPexonTotalExonProtein feature loci*BPlociTotalLenProtein featureProtein feature note
TgenePTPRN2chr20:36149805chr7:157388013ENST0000038941314221004_1010777.0987.0MotifLeucine-based sorting signal
TgenePTPRN2chr20:36149805chr7:157388013ENST0000038941614221004_1010789.0999.0MotifLeucine-based sorting signal
TgenePTPRN2chr20:36149805chr7:157388013ENST0000038941815231004_1010806.01016.0MotifLeucine-based sorting signal
TgenePTPRN2chr20:36149805chr7:157388013ENST0000040432115231004_1010829.01039.0MotifLeucine-based sorting signal
TgenePTPRN2chr20:36149805chr7:157388013ENST000003894131422945_951777.0987.0RegionSubstrate binding
TgenePTPRN2chr20:36149805chr7:157388013ENST000003894161422945_951789.0999.0RegionSubstrate binding
TgenePTPRN2chr20:36149805chr7:157388013ENST000003894181523945_951806.01016.0RegionSubstrate binding
TgenePTPRN2chr20:36149805chr7:157388013ENST000004043211523945_951829.01039.0RegionSubstrate binding

- Not-retained protein feature among the 13 regional features.
PartnerGeneHbpTbpENSTStrandBPexonTotalExonProtein feature loci*BPlociTotalLenProtein featureProtein feature note
TgenePTPRN2chr20:36149805chr7:157388013ENST000003894131422745_1005777.0987.0DomainTyrosine-protein phosphatase
TgenePTPRN2chr20:36149805chr7:157388013ENST000003894161422745_1005789.0999.0DomainTyrosine-protein phosphatase
TgenePTPRN2chr20:36149805chr7:157388013ENST000003894181523745_1005806.01016.0DomainTyrosine-protein phosphatase
TgenePTPRN2chr20:36149805chr7:157388013ENST000004043211523745_1005829.01039.0DomainTyrosine-protein phosphatase
TgenePTPRN2chr20:36149805chr7:157388013ENST000003894131422666_675777.0987.0MotifTyrosine-based internalization motif
TgenePTPRN2chr20:36149805chr7:157388013ENST000003894161422666_675789.0999.0MotifTyrosine-based internalization motif
TgenePTPRN2chr20:36149805chr7:157388013ENST000003894181523666_675806.01016.0MotifTyrosine-based internalization motif
TgenePTPRN2chr20:36149805chr7:157388013ENST000004043211523666_675829.01039.0MotifTyrosine-based internalization motif
TgenePTPRN2chr20:36149805chr7:157388013ENST00000389413142222_615777.0987.0Topological domainExtracellular
TgenePTPRN2chr20:36149805chr7:157388013ENST000003894131422637_1015777.0987.0Topological domainCytoplasmic
TgenePTPRN2chr20:36149805chr7:157388013ENST00000389416142222_615789.0999.0Topological domainExtracellular
TgenePTPRN2chr20:36149805chr7:157388013ENST000003894161422637_1015789.0999.0Topological domainCytoplasmic
TgenePTPRN2chr20:36149805chr7:157388013ENST00000389418152322_615806.01016.0Topological domainExtracellular
TgenePTPRN2chr20:36149805chr7:157388013ENST000003894181523637_1015806.01016.0Topological domainCytoplasmic
TgenePTPRN2chr20:36149805chr7:157388013ENST00000404321152322_615829.01039.0Topological domainExtracellular
TgenePTPRN2chr20:36149805chr7:157388013ENST000004043211523637_1015829.01039.0Topological domainCytoplasmic
TgenePTPRN2chr20:36149805chr7:157388013ENST000003894131422616_636777.0987.0TransmembraneHelical
TgenePTPRN2chr20:36149805chr7:157388013ENST000003894161422616_636789.0999.0TransmembraneHelical
TgenePTPRN2chr20:36149805chr7:157388013ENST000003894181523616_636806.01016.0TransmembraneHelical
TgenePTPRN2chr20:36149805chr7:157388013ENST000004043211523616_636829.01039.0TransmembraneHelical


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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
NNAT
PTPRN2


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 NNAT-PTPRN2


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 NNAT-PTPRN2


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