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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: 11623

FusionGeneSummary for ENO1_UVRAG

check button Fusion gene summary
Fusion gene informationFusion gene name: ENO1_UVRAG
Fusion gene ID: 11623
HgeneTgene
Gene symbol

ENO1

UVRAG

Gene ID

2023

7405

Gene nameenolase 1UV radiation resistance associated
SynonymsENO1L1|HEL-S-17|MPB1|NNE|PPHDHTX|VPS38|p63
Cytomap

1p36.23

11q13.5

Type of geneprotein-codingprotein-coding
Descriptionalpha-enolasec-myc promoter-binding protein-12-phospho-D-glycerate hydro-lyaseMYC promoter-binding protein 1alpha enolase like 1enolase 1, (alpha)enolase-alphaepididymis secretory protein Li 17non-neural enolasephosphopyruvate hydrataseplasminogUV radiation resistance-associated gene proteinbeclin 1 binding proteindisrupted in heterotaxy
Modification date2018052320180523
UniProtAcc

P06733

Q9P2Y5

Ensembl transtripts involved in fusion geneENST00000234590, ENST00000356136, 
ENST00000528420, ENST00000533454, 
ENST00000531818, ENST00000532130, 
ENST00000539288, ENST00000525872, 
ENST00000538870, 
Fusion gene scores* DoF score14 X 15 X 7=147024 X 13 X 11=3432
# samples 2125
** MAII scorelog2(21/1470*10)=-2.8073549220576
possibly effective Gene in Pan-Cancer Fusion Genes (peGinPCFGs).
DoF>8 and MAII<0
log2(25/3432*10)=-3.77904955283746
possibly effective Gene in Pan-Cancer Fusion Genes (peGinPCFGs).
DoF>8 and MAII<0
Context

PubMed: ENO1 [Title/Abstract] AND UVRAG [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
HgeneENO1

GO:0000122

negative regulation of transcription by RNA polymerase II

2005901

HgeneENO1

GO:0030308

negative regulation of cell growth

10082554

HgeneENO1

GO:0045892

negative regulation of transcription, DNA-templated

10082554

HgeneENO1

GO:1903298

negative regulation of hypoxia-induced intrinsic apoptotic signaling pathway

15459207

HgeneENO1

GO:2001171

positive regulation of ATP biosynthetic process

15459207

TgeneUVRAG

GO:0071900

regulation of protein serine/threonine kinase activity

22542840

TgeneUVRAG

GO:0097680

double-strand break repair via classical nonhomologous end joining

22542840


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
TCGARVLUSCTCGA-77-8009-01AENO1chr1

8921061

-UVRAGchr11

75694431

+
* 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
Frame-shiftENST00000234590ENST00000356136ENO1chr1

8921061

-UVRAGchr11

75694431

+
Frame-shiftENST00000234590ENST00000528420ENO1chr1

8921061

-UVRAGchr11

75694431

+
5CDS-5UTRENST00000234590ENST00000533454ENO1chr1

8921061

-UVRAGchr11

75694431

+
5CDS-5UTRENST00000234590ENST00000531818ENO1chr1

8921061

-UVRAGchr11

75694431

+
5CDS-5UTRENST00000234590ENST00000532130ENO1chr1

8921061

-UVRAGchr11

75694431

+
5CDS-intronENST00000234590ENST00000539288ENO1chr1

8921061

-UVRAGchr11

75694431

+
5CDS-intronENST00000234590ENST00000525872ENO1chr1

8921061

-UVRAGchr11

75694431

+
5CDS-intronENST00000234590ENST00000538870ENO1chr1

8921061

-UVRAGchr11

75694431

+

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FusionProtFeatures for ENO1_UVRAG


check buttonMain function of each fusion partner protein. (from UniProt)
HgeneTgene
ENO1

P06733

UVRAG

Q9P2Y5

Versatile protein that is involved in regulation ofdifferent cellular pathways implicated in membrane trafficking.Involved in regulation of the COPI-dependent retrograde transportfrom Golgi and the endoplasmic reticulum by associating with theNRZ complex; the function is dependent on its binding tophosphatidylinositol 3-phosphate (PtdIns(3)P) (PubMed:24056303).During autophagy acts as regulatory subunit of the alternativePI3K complex II (PI3KC3-C2) that mediates formation ofphosphatidylinositol 3-phosphate and is believed to be involved inmaturation of autophagosomes and endocytosis. Activates lipidkinase activity of PIK3C3. Involved in the regulation ofdegradative endocytic trafficking and cytokinesis, and inregulation of ATG9A transport from the Golgi to the autophagosome;the functions seems to implicate its association with PI3KC3-C2(PubMed:16799551, PubMed:20643123, PubMed:24056303). Involved inmaturation of autophagosomes and degradative endocytic traffickingindependently of BECN1 but depending on its association with aclass C Vps complex (possibly the HOPS complex); the associationis also proposed to promote autophagosome recruitment andactivation of Rab7 and endosome-endosome fusion events(PubMed:18552835). Enhances class C Vps complex (possibly HOPScomplex) association with a SNARE complex and promotes fusogenicSNARE complex formation during late endocytic membrane fusion(PubMed:24550300). In case of negative-strand RNA virus infectionis required for efficient virus entry, promotes endocytictransport of virions and is implicated in a VAMP8-specificfusogenic SNARE complex assembly (PubMed:24550300).{ECO:0000269|PubMed:18552835, ECO:0000269|PubMed:20643123,ECO:0000269|PubMed:24056303, ECO:0000305}. Involved in maintaining chromosomal stability. PromotesDNA double-strand break (DSB) repair by association with DNA-dependent protein kinase complex DNA-PK and activating it in non-homologous end joining (NHEJ) (PubMed:22542840). Required forcentrosome stability and proper chromosome segregation(PubMed:22542840). {ECO:0000269|PubMed:22542840}.

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 ENO1_UVRAG


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 ENO1_UVRAG


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
ENO1FANCA, PLG, TRAPPC2, ISG15, MAP2K5, HDAC1, H2AFX, CD4, YWHAZ, INSIG2, PCNA, GRB2, PSMA3, FBXO25, CUL3, CUL4A, CUL4B, CUL5, CUL2, CDK2, CUL1, COPS5, CAND1, MYOC, IVNS1ABP, AGTPBP1, AKT1, FYN, SRC, PGK1, GAPDH, TPI1, FLNC, PPIA, ITPA, ENO3, BRCA1, LIG4, MDC1, VCAM1, FN1, ATF2, ITGA4, NPM1, RAD52, TERT, AMBP, SERPING1, BHLHE40, UPF2, YWHAQ, FBXO6, WWOX, STAU1, HUWE1, FUS, SZRD1, NUDC, RCC1, YARS, LRRC42, MRPL37, DPH5, GSTM3, STRIP1, HIST2H2AB, CDC42SE1, POGZ, LMNA, HDGF, DEDD, TOMM40L, STX6, SRSF7, EFEMP1, CCT7, POLR1A, BIN1, IWS1, NAB1, ABI2, EEF1B2, ARPC4, SNORA6, DHX30, QRICH1, IFRD2, THOC7, DHX15, HNRNPD, FAT4, DCLK2, ERAP1, RAPGEF6, HSPA9, STK10, FARS2, HIST1H2BG, HIST1H4I, KLHDC3, MYO6, ASCC3, HDAC2, FBXO5, SCAF8, OSBPL3, OGDH, TNS3, GATAD1, PMPCB, NUP205, XPO7, SCARA3, MTFR1, C8orf33, KANK1, MPDZ, ACO1, UBAP1, ANXA1, POLE3, HNRNPH3, BTRC, NAP1L4, COPB1, CAT, PRPF19, CPSF7, SYT12, CPT1A, NUMA1, ENDOD1, YAP1, DCPS, NCAPD3, VPS26B, M6PR, PPFIBP1, LETMD1, RBMS2, NTN4, MVK, RNF10, RHOF, STX2, MPHOSPH8, DIAPH3, MBNL2, CARKD, PNP, IPO4, RBM25, C14orf1, KNSTRN, TP53BP1, MYO1E, KIF23, PTPN9, SNRNP25, STUB1, TXNDC11, VPS35, E2F4, NFATC3, CYB5B, PDPR, AARS, WDR81, CHD3, RAB34, MYO18A, ACACA, THRA, SMARCE1, DHX8, SLC25A39, ANKRD40, LUC7L3, NPLOC4, CEP192, GIPC3, HNRNPM, CRLF1, MED29, SUPT5H, FBL, PPP5C, ISOC2, NOP56, XRN2, POFUT1, CEP250, ZNFX1, ATP5J, SUMO3, CLTCL1, PITPNB, NIPSNAP1, SF3A1, XRCC6, CYB5R3, TXLNG, SH3KBP1, PRDX4, POLA1, EBP, MORC4, BCAP31, CUL7, OBSL1, CCDC8, EED, EMC1, TXNDC16, FAF2, SUMO2, ENO2, HNRNPA1, AKR1B1, AKR1B15, CALR, DUT, EEF2, ABAT, ACAA2, ALDH4A1, ALDOA, CFL1, EZR, FH, FKBP2, GPX4, HINT1, HSD17B10, LDHA, LDHB, MSN, NME1-NME2, NME2, PARK7, PCMT1, PDCD6IP, PGK2, PGM1, PPIB, RCN1, RDX, SOD1, TAGLN, TAGLN2, TAGLN3, TKT, WDR1, FABP5, FKBP1A, FKBP1B, FKBP7, GPI, MIF, NIT2, P4HB, PEF1, PGAM1, PMP2, PUS7, SRI, TALDO1, TXN, UCHL3, NTRK1, HSPB2, CHEK2, CLK1, AHSA1, ATP6AP2, HEMGN, MCM2, MCM5, FBXW7, CDC73, ATOH1, WWP2, CDH1, SLC9A1, TRIM25, MCPH1, HDAC6UVRAGBECN1, PIK3C3, VPS33A, VPS18, PIK3R4, PTPRA, KIAA0226, TGFBRAP1, VPS16, VPS11, VPS33B, VPS39, YWHAE, RALB, USP18, XPO1, MYO1C, DDB1, DDB2, CUL4A, RBX1, KIAA0226L


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 ENO1_UVRAG


check button Drugs targeting genes involved in this fusion gene.
(DrugBank Version 5.1.0 2018-04-02)
PartnerGeneUniProtAccDrugBank IDDrug nameDrug activityDrug typeDrug status
HgeneENO1P06733DB01593ZincAlpha-enolasesmall moleculeapproved|investigational
HgeneENO1P06733DB11638ArtenimolAlpha-enolasesmall moleculeapproved|investigational

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RelatedDiseases for ENO1_UVRAG


check button Diseases associated with fusion partners.
(DisGeNet 4.0)
PartnerGeneDisease IDDisease name# pubmedsSource
HgeneENO1C0001418Adenocarcinoma1CTD_human
HgeneENO1C0002395Alzheimer's Disease1CTD_human
HgeneENO1C0003873Rheumatoid Arthritis1CTD_human
HgeneENO1C0007131Non-Small Cell Lung Carcinoma1CTD_human
HgeneENO1C0007137Squamous cell carcinoma1CTD_human
HgeneENO1C0014859Esophageal Neoplasms1CTD_human
HgeneENO1C0021364Male infertility1CTD_human
HgeneENO1C0024667Animal Mammary Neoplasms1CTD_human
HgeneENO1C0024668Mammary Neoplasms, Experimental1CTD_human
HgeneENO1C0026640Mouth Neoplasms1CTD_human
HgeneENO1C0027626Neoplasm Invasiveness1CTD_human
HgeneENO1C0029408Degenerative polyarthritis1CTD_human
HgeneENO1C0029456Osteoporosis1CTD_human
HgeneENO1C0036341Schizophrenia1PSYGENET
HgeneENO1C0038356Stomach Neoplasms1CTD_human
HgeneENO1C0152013Adenocarcinoma of lung (disorder)1CTD_human
HgeneENO1C0520459Necrotizing Enterocolitis1CTD_human
HgeneENO1C0948089Acute Coronary Syndrome1CTD_human
HgeneENO1C1458155Mammary Neoplasms1CTD_human
HgeneENO1C2239176Liver carcinoma1CTD_human
HgeneENO1C4277682Chemical and Drug Induced Liver Injury1CTD_human