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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: 11624

FusionGeneSummary for ENO2_PIANP

check button Fusion gene summary
Fusion gene informationFusion gene name: ENO2_PIANP
Fusion gene ID: 11624
HgeneTgene
Gene symbol

ENO2

PIANP

Gene ID

2026

196500

Gene nameenolase 2PILR alpha associated neural protein
SynonymsHEL-S-279|NSEC12orf53|LEDA1|PANP|leda-1
Cytomap

12p13.31

12p13.31

Type of geneprotein-codingprotein-coding
Descriptiongamma-enolase2-phospho-D-glycerate hydro-lyase2-phospho-D-glycerate hydrolyaseenolase 2 (gamma, neuronal)epididymis secretory protein Li 279neural enolaseneuron specific gamma enolaseneuron-specific enolaseneuronal enriched enolaseneurone-specifiPILR alpha-associated neural proteinPILR-associating neural proteinliver endothelial differentiation-associated protein-1paired immunoglobin-like type 2 receptor-associating neural protein
Modification date2018051920180519
UniProtAcc

P09104

Q8IYJ0

Ensembl transtripts involved in fusion geneENST00000541477, ENST00000229277, 
ENST00000538763, ENST00000544774, 
ENST00000545045, ENST00000535366, 
ENST00000534977, 
ENST00000540656, 
ENST00000320591, ENST00000534837, 
Fusion gene scores* DoF score2 X 2 X 2=82 X 1 X 2=4
# samples 22
** MAII scorelog2(2/8*10)=1.32192809488736log2(2/4*10)=2.32192809488736
Context

PubMed: ENO2 [Title/Abstract] AND PIANP [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

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
TCGALDCOADTCGA-G4-6626-01AENO2chr12

7023823

+PIANPchr12

6807270

-
* 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
5UTR-5UTRENST00000541477ENST00000540656ENO2chr12

7023823

+PIANPchr12

6807270

-
5UTR-5UTRENST00000541477ENST00000320591ENO2chr12

7023823

+PIANPchr12

6807270

-
5UTR-5UTRENST00000541477ENST00000534837ENO2chr12

7023823

+PIANPchr12

6807270

-
5UTR-5UTRENST00000229277ENST00000540656ENO2chr12

7023823

+PIANPchr12

6807270

-
5UTR-5UTRENST00000229277ENST00000320591ENO2chr12

7023823

+PIANPchr12

6807270

-
5UTR-5UTRENST00000229277ENST00000534837ENO2chr12

7023823

+PIANPchr12

6807270

-
5UTR-5UTRENST00000538763ENST00000540656ENO2chr12

7023823

+PIANPchr12

6807270

-
5UTR-5UTRENST00000538763ENST00000320591ENO2chr12

7023823

+PIANPchr12

6807270

-
5UTR-5UTRENST00000538763ENST00000534837ENO2chr12

7023823

+PIANPchr12

6807270

-
5UTR-5UTRENST00000544774ENST00000540656ENO2chr12

7023823

+PIANPchr12

6807270

-
5UTR-5UTRENST00000544774ENST00000320591ENO2chr12

7023823

+PIANPchr12

6807270

-
5UTR-5UTRENST00000544774ENST00000534837ENO2chr12

7023823

+PIANPchr12

6807270

-
5UTR-5UTRENST00000545045ENST00000540656ENO2chr12

7023823

+PIANPchr12

6807270

-
5UTR-5UTRENST00000545045ENST00000320591ENO2chr12

7023823

+PIANPchr12

6807270

-
5UTR-5UTRENST00000545045ENST00000534837ENO2chr12

7023823

+PIANPchr12

6807270

-
intron-5UTRENST00000535366ENST00000540656ENO2chr12

7023823

+PIANPchr12

6807270

-
intron-5UTRENST00000535366ENST00000320591ENO2chr12

7023823

+PIANPchr12

6807270

-
intron-5UTRENST00000535366ENST00000534837ENO2chr12

7023823

+PIANPchr12

6807270

-
intron-5UTRENST00000534977ENST00000540656ENO2chr12

7023823

+PIANPchr12

6807270

-
intron-5UTRENST00000534977ENST00000320591ENO2chr12

7023823

+PIANPchr12

6807270

-
intron-5UTRENST00000534977ENST00000534837ENO2chr12

7023823

+PIANPchr12

6807270

-

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FusionProtFeatures for ENO2_PIANP


check buttonMain function of each fusion partner protein. (from UniProt)
HgeneTgene
ENO2

P09104

PIANP

Q8IYJ0

Has neurotrophic and neuroprotective properties on abroad spectrum of central nervous system (CNS) neurons. Binds, ina calcium-dependent manner, to cultured neocortical neurons andpromotes cell survival (By similarity). {ECO:0000250}. Acts as a ligand for PILRA in neural tissues, where itmay be involved in immune regulation.{ECO:0000269|PubMed:21241660}.

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 ENO2_PIANP


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 ENO2_PIANP


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
ENO2C16orf45, C6orf47, HSF1, IL17B, NDUFS7, ST3GAL2, SIGIRR, UBE2C, ANXA11, ENSA, HABP4, MAP4, SNUPN, NAT9, HK1, TUBA4A, TERF1, TINF2, ACD, POT1, PPP1CC, CUL3, CUL4B, CUL2, CDK2, CUL1, CAND1, AKT1, A2M, COASY, EFHD2, GMPS, PNP, RAB1A, RCN1, ASB5, ASB9, EXOC5, ENO1, ENO3, NTRK1, AKR1B1, AKR1B15, ARHGDIA, CALR, DUT, EEF1A1, CTH, EZR, FKBP2, GAPDH, GPX4, HINT1, HSD17B10, MSN, NME1-NME2, NME2, PCMT1, PGK1, PLS3, PPIB, SEC31A, SOD1, STIP1, TAGLN, TAGLN2, TAGLN3, TKT, TPD52, WDR1, FABP5, FKBP1A, FKBP1B, FKBP7, HSPE1, PGAM1, PUS7, SUMO2, SUMO3, TPI1, TXN, UCHL3, PTEN, POC1A, CENPJ, MTNR1APIANPGALNT4, ADCY9, GALNT12, PRUNE, AKT3, LRRC16A, PTPRD, FAM115C, GALNT2, PTPRF, GHITM


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 ENO2_PIANP


check button Drugs targeting genes involved in this fusion gene.
(DrugBank Version 5.1.0 2018-04-02)
PartnerGeneUniProtAccDrugBank IDDrug nameDrug activityDrug typeDrug status

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RelatedDiseases for ENO2_PIANP


check button Diseases associated with fusion partners.
(DisGeNet 4.0)
PartnerGeneDisease IDDisease name# pubmedsSource
HgeneENO2C0005695Bladder Neoplasm1CTD_human
HgeneENO2C0007131Non-Small Cell Lung Carcinoma1CTD_human
HgeneENO2C0007621Neoplastic Cell Transformation1CTD_human
HgeneENO2C0023467Leukemia, Myelocytic, Acute1CTD_human
HgeneENO2C0023904Liver Neoplasms, Experimental1CTD_human
HgeneENO2C0027659Neoplasms, Experimental1CTD_human
HgeneENO2C0036341Schizophrenia1PSYGENET