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Center for Computational Systems Medicine
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FusionGeneSummary

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FusionProtFeature

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FusionGeneSequence

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FusionGenePPI

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RelatedDrugs

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RelatedDiseases

Fusion gene ID: 29435

FusionGeneSummary for PTPN1_PRR11

check button Fusion gene summary
Fusion gene informationFusion gene name: PTPN1_PRR11
Fusion gene ID: 29435
HgeneTgene
Gene symbol

PTPN1

PRR11

Gene ID

5770

55771

Gene nameprotein tyrosine phosphatase, non-receptor type 1proline rich 11
SynonymsPTP1B-
Cytomap

20q13.13

17q22

Type of geneprotein-codingprotein-coding
Descriptiontyrosine-protein phosphatase non-receptor type 1protein tyrosine phosphatase, placentalprotein-tyrosine phosphatase 1Bproline-rich protein 11transcription repressor of MHCII
Modification date2018052220180523
UniProtAcc

P18031

Q96HE9

Ensembl transtripts involved in fusion geneENST00000371621, ENST00000541713, 
ENST00000262293, 
Fusion gene scores* DoF score7 X 4 X 5=1406 X 1 X 4=24
# samples 86
** MAII scorelog2(8/140*10)=-0.807354922057604
possibly effective Gene in Pan-Cancer Fusion Genes (peGinPCFGs).
DoF>8 and MAII<0
log2(6/24*10)=1.32192809488736
effective Gene in Pan-Cancer Fusion Genes (eGinPCFGs).
DoF>8 and MAII>0
Context

PubMed: PTPN1 [Title/Abstract] AND PRR11 [Title/Abstract] AND fusion [Title/Abstract]

Functional or gene categories assigned by FusionGDB annotation
* 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
HgenePTPN1

GO:0030100

regulation of endocytosis

21135139

HgenePTPN1

GO:0030968

endoplasmic reticulum unfolded protein response

22169477

HgenePTPN1

GO:0035335

peptidyl-tyrosine dephosphorylation

21135139

HgenePTPN1

GO:0061098

positive regulation of protein tyrosine kinase activity

21216966

HgenePTPN1

GO:1903898

negative regulation of PERK-mediated unfolded protein response

21216966

TgenePRR11

GO:0051726

regulation of cell cycle

23246489


check button Fusion gene information from three resources
(ChiTars (NAR, 2018), tumorfusions (NAR, 2018), Gao et al. (Cell, 2018))
* 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.
Data typeSourceCancer typeSampleHgeneHchrHbpHstrandTgeneTchrTbpTstrand
TCGARVSTADTCGA-D7-A6EZ-01APTPN1chr20

49185015

+PRR11chr17

57247109

+
* LD: Li Ding group's fusion gene list
  RV: Roel Verhaak group's fusion gene list
  ChiTaRs fusion database

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
5CDS-5UTRENST00000371621ENST00000262293PTPN1chr20

49185015

+PRR11chr17

57247109

+
5CDS-5UTRENST00000541713ENST00000262293PTPN1chr20

49185015

+PRR11chr17

57247109

+

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FusionProtFeatures for PTPN1_PRR11


check buttonMain function of each fusion partner protein. (from UniProt)
HgeneTgene
PTPN1

P18031

PRR11

Q96HE9

Tyrosine-protein phosphatase which acts as a regulatorof endoplasmic reticulum unfolded protein response. Mediatesdephosphorylation of EIF2AK3/PERK; inactivating the protein kinaseactivity of EIF2AK3/PERK. May play an important role in CKII- andp60c-src-induced signal transduction cascades. May regulate theEFNA5-EPHA3 signaling pathway which modulates cell reorganizationand cell-cell repulsion. May also regulate the hepatocyte growthfactor receptor signaling pathway through dephosphorylation ofMET. {ECO:0000269|PubMed:18819921, ECO:0000269|PubMed:21135139,ECO:0000269|PubMed:22169477}. Plays a critical role in cell cycle progression.{ECO:0000269|PubMed:23246489}.

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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FusionGeneSequence for PTPN1_PRR11


check button For in-frame fusion transcripts, we provide the fusion transcript sequences and fusion amino acid sequences.
(nt: nucleotides, aa: amino acids)

* Fusion amino acid sequences.

* Fusion transcript sequences (only coding sequence (CDS) region).

* Fusion transcript sequences (Full-length transcript).

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FusionGenePPI for PTPN1_PRR11


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
PTPN1GSK3B, GRB2, IRS1, CAV1, EGFR, CRK, BCAR1, CTNNB1, STAT5A, STAT5B, NTRK1, NTRK2, NTRK3, LTK, TYK2, JAK2, INSR, IGF1R, GHR, STAM2, ILF3, SLC25A3, MCAT, MARCKSL1, LAMTOR3, HNRNPU, ZMPSTE24, STAT3, ATF2, CSNK2A1, SRC, ATP4A, ASS1, RFWD2, IL1B, ASGR2, HMOX2, SLC39A4, LYPD3, ENPP6, ZACN, PLTP, LYPD6, KRAS, AGR3, BCAS3, CASC3, CASZ1, CCL5, CDH13, DIRAS3, FAM84B, KLK7, MRC2, RHOBTB2, SNAI1, THRSP, VPS45, HERC2, TCTN2, TCTN3, EVC2, TMEM17, TMEM216, ATP6V1B2, ATP6V0A1, COL5A1, STOM, FLOT2, GALNT2, MSN, PHB, ABCD3, SMARCD2, ATP6V0D1, GOSR1, MVP, FLOT1, PHB2, LTN1, GOLIM4, BCOR, WRAP53, MREG, PCNP, KIDINS220, RNF213, ARHGAP39, PTRF, CDH1, ACTB, APLP2, CASC4, SNRPD2, TOMM70A, CTDNEP1, C5AR2, TMEM63A, C3AR1, GPR21, GHITM, SLCO6A1, TMPRSS3, AMTN, MRAP2, GPR114, KIAA1467, SLC39A12, APLNR, DUSP1, DCUN1D5, PISD, COX11, NDUFAF4, NARS, PTRH2, TBC1D15, NPPC, PFN2, ARL1, DHCR24, AIP, RAB5C, PGRMC1, SEC61A1, CDIPT, SLC27A4, ILVBL, DHCR7, TRIP13, ARF4, HEATR3, PCMT1, ARF1, CCDC47, CDK4, FLAD1, RMDN3, CLK2, LATPRR11NIP7, KNOP1, RBM28, SF3B1, POP1, DDX24, FTSJ3, SF3B2, ZNF668, RPL3, UPF1, ZNF512, RPL10A, DKC1, PABPC4, DHX30, ELAVL2, DDX27, HIST1H1A, GLYR1, SORD, HP1BP3, REXO4, DDX31, MYBBP1A, NOP16, RPL26L1, RPS3A, KRI1, WHSC1, C7orf50, ZCRB1, EBNA1BP2, UTP23, ZCCHC3, RRP12, RSBN1, TTF1, SURF6, LARP1, LYAR, RRP8, STAU2, STAU1, CTCF, NVL, GLTSCR2, LLPH, RPS15, GPATCH4, CCDC86, RBM34, LIN28B, NOC4L, NOC3L, BRIX1, NOP2, RSL24D1, TSR1, MOV10, PWP1, RRS1, KRR1, RPL15, KIAA0020, PAK1IP1, RPL23A, GNL2, RPS13, ZBTB24, ZNF771, ZBTB11, RPL13A, PRDM15, RPL7L1, RPF2, ZNF800, PES1, CASC3, PURA, PPAN-P2RY11, NSA2, ZNF22, NOL12, ZNF189, MRPL38, ZNF689, DUSP11, OSBPL5, IL4R, RPL18A, RPS3, RPL4, BOP1


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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RelatedDrugs for PTPN1_PRR11


check button Drugs targeting genes involved in this fusion gene.
(DrugBank Version 5.1.0 2018-04-02)
PartnerGeneUniProtAccDrugBank IDDrug nameDrug activityDrug typeDrug status
HgenePTPN1P18031DB01133Tiludronic acidTyrosine-protein phosphatase non-receptor type 1small moleculeapproved|investigational|vet_approved

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RelatedDiseases for PTPN1_PRR11


check button Diseases associated with fusion partners.
(DisGeNet 4.0)
PartnerGeneDisease IDDisease name# pubmedsSource
HgenePTPN1C0019829Hodgkin Disease1CTD_human
HgenePTPN1C0021655Insulin Resistance1CTD_human
HgenePTPN1C0023893Liver Cirrhosis, Experimental1CTD_human
HgenePTPN1C0025063Mediastinal Neoplasms1CTD_human
HgenePTPN1C0028754Obesity1CTD_human
HgenePTPN1C0035372Rett Syndrome1CTD_human
HgenePTPN1C0036341Schizophrenia1PSYGENET
HgenePTPN1C0079731B-Cell Lymphomas1CTD_human