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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: 24046

FusionGeneSummary for NEMF_WWOX

check button Fusion gene summary
Fusion gene informationFusion gene name: NEMF_WWOX
Fusion gene ID: 24046
HgeneTgene
Gene symbol

NEMF

WWOX

Gene ID

9147

51741

Gene namenuclear export mediator factorWW domain containing oxidoreductase
SynonymsNY-CO-1|SDCCAG1D16S432E|EIEE28|FOR|FRA16D|HHCMA56|PRO0128|SCAR12|SDR41C1|WOX1
Cytomap

14q21.3

16q23.1-q23.2

Type of geneprotein-codingprotein-coding
Descriptionnuclear export mediator factor NEMFantigen NY-CO-1serologically defined colon cancer antigen 1WW domain-containing oxidoreductaseWW domain-containing protein WWOXfragile site FRA16D oxidoreductaseshort chain dehydrogenase/reductase family 41C member 1
Modification date2018052320180523
UniProtAcc

O60524

Q9NZC7

Ensembl transtripts involved in fusion geneENST00000298310, ENST00000382135, 
ENST00000545773, ENST00000556925, 
ENST00000546046, ENST00000556672, 
ENST00000566780, ENST00000406884, 
ENST00000539474, ENST00000402655, 
ENST00000408984, ENST00000355860, 
ENST00000565791, ENST00000569818, 
Fusion gene scores* DoF score11 X 16 X 5=88014 X 7 X 7=686
# samples 1816
** MAII scorelog2(18/880*10)=-2.28950661719499
possibly effective Gene in Pan-Cancer Fusion Genes (peGinPCFGs).
DoF>8 and MAII<0
log2(16/686*10)=-2.10013667128545
possibly effective Gene in Pan-Cancer Fusion Genes (peGinPCFGs).
DoF>8 and MAII<0
Context

PubMed: NEMF [Title/Abstract] AND WWOX [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
TgeneWWOX

GO:0030178

negative regulation of Wnt signaling pathway

19465938

TgeneWWOX

GO:0071560

cellular response to transforming growth factor beta stimulus

19366691


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
ChiTaRS3.1BX092681NEMFchr14

50096467

-WWOXchr16

78272007

-
ChiTaRS3.1AW874698NEMFchr14

50096467

-WWOXchr16

78272007

-
* 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
intron-intronENST00000298310ENST00000566780NEMFchr14

50096467

-WWOXchr16

78272007

-
intron-intronENST00000298310ENST00000406884NEMFchr14

50096467

-WWOXchr16

78272007

-
intron-intronENST00000298310ENST00000539474NEMFchr14

50096467

-WWOXchr16

78272007

-
intron-intronENST00000298310ENST00000402655NEMFchr14

50096467

-WWOXchr16

78272007

-
intron-intronENST00000298310ENST00000408984NEMFchr14

50096467

-WWOXchr16

78272007

-
intron-intronENST00000298310ENST00000355860NEMFchr14

50096467

-WWOXchr16

78272007

-
intron-intronENST00000298310ENST00000565791NEMFchr14

50096467

-WWOXchr16

78272007

-
intron-intronENST00000298310ENST00000569818NEMFchr14

50096467

-WWOXchr16

78272007

-
intron-intronENST00000382135ENST00000566780NEMFchr14

50096467

-WWOXchr16

78272007

-
intron-intronENST00000382135ENST00000406884NEMFchr14

50096467

-WWOXchr16

78272007

-
intron-intronENST00000382135ENST00000539474NEMFchr14

50096467

-WWOXchr16

78272007

-
intron-intronENST00000382135ENST00000402655NEMFchr14

50096467

-WWOXchr16

78272007

-
intron-intronENST00000382135ENST00000408984NEMFchr14

50096467

-WWOXchr16

78272007

-
intron-intronENST00000382135ENST00000355860NEMFchr14

50096467

-WWOXchr16

78272007

-
intron-intronENST00000382135ENST00000565791NEMFchr14

50096467

-WWOXchr16

78272007

-
intron-intronENST00000382135ENST00000569818NEMFchr14

50096467

-WWOXchr16

78272007

-
intron-intronENST00000545773ENST00000566780NEMFchr14

50096467

-WWOXchr16

78272007

-
intron-intronENST00000545773ENST00000406884NEMFchr14

50096467

-WWOXchr16

78272007

-
intron-intronENST00000545773ENST00000539474NEMFchr14

50096467

-WWOXchr16

78272007

-
intron-intronENST00000545773ENST00000402655NEMFchr14

50096467

-WWOXchr16

78272007

-
intron-intronENST00000545773ENST00000408984NEMFchr14

50096467

-WWOXchr16

78272007

-
intron-intronENST00000545773ENST00000355860NEMFchr14

50096467

-WWOXchr16

78272007

-
intron-intronENST00000545773ENST00000565791NEMFchr14

50096467

-WWOXchr16

78272007

-
intron-intronENST00000545773ENST00000569818NEMFchr14

50096467

-WWOXchr16

78272007

-
intron-intronENST00000556925ENST00000566780NEMFchr14

50096467

-WWOXchr16

78272007

-
intron-intronENST00000556925ENST00000406884NEMFchr14

50096467

-WWOXchr16

78272007

-
intron-intronENST00000556925ENST00000539474NEMFchr14

50096467

-WWOXchr16

78272007

-
intron-intronENST00000556925ENST00000402655NEMFchr14

50096467

-WWOXchr16

78272007

-
intron-intronENST00000556925ENST00000408984NEMFchr14

50096467

-WWOXchr16

78272007

-
intron-intronENST00000556925ENST00000355860NEMFchr14

50096467

-WWOXchr16

78272007

-
intron-intronENST00000556925ENST00000565791NEMFchr14

50096467

-WWOXchr16

78272007

-
intron-intronENST00000556925ENST00000569818NEMFchr14

50096467

-WWOXchr16

78272007

-
intron-intronENST00000546046ENST00000566780NEMFchr14

50096467

-WWOXchr16

78272007

-
intron-intronENST00000546046ENST00000406884NEMFchr14

50096467

-WWOXchr16

78272007

-
intron-intronENST00000546046ENST00000539474NEMFchr14

50096467

-WWOXchr16

78272007

-
intron-intronENST00000546046ENST00000402655NEMFchr14

50096467

-WWOXchr16

78272007

-
intron-intronENST00000546046ENST00000408984NEMFchr14

50096467

-WWOXchr16

78272007

-
intron-intronENST00000546046ENST00000355860NEMFchr14

50096467

-WWOXchr16

78272007

-
intron-intronENST00000546046ENST00000565791NEMFchr14

50096467

-WWOXchr16

78272007

-
intron-intronENST00000546046ENST00000569818NEMFchr14

50096467

-WWOXchr16

78272007

-
intron-intronENST00000556672ENST00000566780NEMFchr14

50096467

-WWOXchr16

78272007

-
intron-intronENST00000556672ENST00000406884NEMFchr14

50096467

-WWOXchr16

78272007

-
intron-intronENST00000556672ENST00000539474NEMFchr14

50096467

-WWOXchr16

78272007

-
intron-intronENST00000556672ENST00000402655NEMFchr14

50096467

-WWOXchr16

78272007

-
intron-intronENST00000556672ENST00000408984NEMFchr14

50096467

-WWOXchr16

78272007

-
intron-intronENST00000556672ENST00000355860NEMFchr14

50096467

-WWOXchr16

78272007

-
intron-intronENST00000556672ENST00000565791NEMFchr14

50096467

-WWOXchr16

78272007

-
intron-intronENST00000556672ENST00000569818NEMFchr14

50096467

-WWOXchr16

78272007

-

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FusionProtFeatures for NEMF_WWOX


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

O60524

WWOX

Q9NZC7


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 NEMF_WWOX


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 NEMF_WWOX


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


Top

RelatedDrugs for NEMF_WWOX


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 NEMF_WWOX


check button Diseases associated with fusion partners.
(DisGeNet 4.0)
PartnerGeneDisease IDDisease name# pubmedsSource
TgeneWWOXC0007137Squamous cell carcinoma1CTD_human
TgeneWWOXC0038356Stomach Neoplasms1CTD_human
TgeneWWOXC0042076Urologic Neoplasms1CTD_human
TgeneWWOXC0279626Squamous cell carcinoma of esophagus1CTD_human
TgeneWWOXC1458155Mammary Neoplasms1CTD_human
TgeneWWOXC3280452SPINOCEREBELLAR ATAXIA, AUTOSOMAL RECESSIVE 121ORPHANET;UNIPROT
TgeneWWOXC3495559Juvenile arthritis1CTD_human
TgeneWWOXC4015519EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 281UNIPROT