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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: 25285

FusionGeneSummary for NVL_WDR26

check button Fusion gene summary
Fusion gene informationFusion gene name: NVL_WDR26
Fusion gene ID: 25285
HgeneTgene
Gene symbol

NVL

WDR26

Gene ID

4931

80232

Gene namenuclear VCP-likeWD repeat domain 26
SynonymsNVL2CDW2|GID7|MIP2|SKDEAS
Cytomap

1q42.11

1q42.11-q42.12

Type of geneprotein-codingprotein-coding
Descriptionnuclear valosin-containing protein-likeNVLpWD repeat-containing protein 26CUL4- and DDB1-associated WDR protein 2GID complex subunit 7 homologmyocardial ischemic preconditioning upregulated protein 2
Modification date2018052320180522
UniProtAcc

O15381

Q9H7D7

Ensembl transtripts involved in fusion geneENST00000391875, ENST00000281701, 
ENST00000469075, ENST00000482491, 
ENST00000340871, ENST00000361463, 
ENST00000468673, 
ENST00000414423, 
ENST00000295024, ENST00000366852, 
ENST00000479727, 
Fusion gene scores* DoF score8 X 6 X 6=2885 X 6 X 4=120
# samples 76
** MAII scorelog2(7/288*10)=-2.04064198449735
possibly effective Gene in Pan-Cancer Fusion Genes (peGinPCFGs).
DoF>8 and MAII<0
log2(6/120*10)=-1
possibly effective Gene in Pan-Cancer Fusion Genes (peGinPCFGs).
DoF>8 and MAII<0
Context

PubMed: NVL [Title/Abstract] AND WDR26 [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
TCGALDBRCATCGA-C8-A12K-01ANVLchr1

224499502

-WDR26chr1

224574204

-
TCGARVUCSTCGA-N6-A4VG-01ANVLchr1

224499502

-WDR26chr1

224577562

-
* 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-3UTRENST00000391875ENST00000414423NVLchr1

224499502

-WDR26chr1

224574204

-
5CDS-3UTRENST00000391875ENST00000295024NVLchr1

224499502

-WDR26chr1

224574204

-
5CDS-intronENST00000391875ENST00000366852NVLchr1

224499502

-WDR26chr1

224574204

-
5CDS-intronENST00000391875ENST00000479727NVLchr1

224499502

-WDR26chr1

224574204

-
5CDS-3UTRENST00000281701ENST00000414423NVLchr1

224499502

-WDR26chr1

224574204

-
5CDS-3UTRENST00000281701ENST00000295024NVLchr1

224499502

-WDR26chr1

224574204

-
5CDS-intronENST00000281701ENST00000366852NVLchr1

224499502

-WDR26chr1

224574204

-
5CDS-intronENST00000281701ENST00000479727NVLchr1

224499502

-WDR26chr1

224574204

-
5CDS-3UTRENST00000469075ENST00000414423NVLchr1

224499502

-WDR26chr1

224574204

-
5CDS-3UTRENST00000469075ENST00000295024NVLchr1

224499502

-WDR26chr1

224574204

-
5CDS-intronENST00000469075ENST00000366852NVLchr1

224499502

-WDR26chr1

224574204

-
5CDS-intronENST00000469075ENST00000479727NVLchr1

224499502

-WDR26chr1

224574204

-
intron-3UTRENST00000482491ENST00000414423NVLchr1

224499502

-WDR26chr1

224574204

-
intron-3UTRENST00000482491ENST00000295024NVLchr1

224499502

-WDR26chr1

224574204

-
intron-intronENST00000482491ENST00000366852NVLchr1

224499502

-WDR26chr1

224574204

-
intron-intronENST00000482491ENST00000479727NVLchr1

224499502

-WDR26chr1

224574204

-
intron-3UTRENST00000340871ENST00000414423NVLchr1

224499502

-WDR26chr1

224574204

-
intron-3UTRENST00000340871ENST00000295024NVLchr1

224499502

-WDR26chr1

224574204

-
intron-intronENST00000340871ENST00000366852NVLchr1

224499502

-WDR26chr1

224574204

-
intron-intronENST00000340871ENST00000479727NVLchr1

224499502

-WDR26chr1

224574204

-
5CDS-3UTRENST00000361463ENST00000414423NVLchr1

224499502

-WDR26chr1

224574204

-
5CDS-3UTRENST00000361463ENST00000295024NVLchr1

224499502

-WDR26chr1

224574204

-
5CDS-intronENST00000361463ENST00000366852NVLchr1

224499502

-WDR26chr1

224574204

-
5CDS-intronENST00000361463ENST00000479727NVLchr1

224499502

-WDR26chr1

224574204

-
intron-3UTRENST00000468673ENST00000414423NVLchr1

224499502

-WDR26chr1

224574204

-
intron-3UTRENST00000468673ENST00000295024NVLchr1

224499502

-WDR26chr1

224574204

-
intron-intronENST00000468673ENST00000366852NVLchr1

224499502

-WDR26chr1

224574204

-
intron-intronENST00000468673ENST00000479727NVLchr1

224499502

-WDR26chr1

224574204

-
Frame-shiftENST00000391875ENST00000414423NVLchr1

224499502

-WDR26chr1

224577562

-
Frame-shiftENST00000391875ENST00000295024NVLchr1

224499502

-WDR26chr1

224577562

-
5CDS-3UTRENST00000391875ENST00000366852NVLchr1

224499502

-WDR26chr1

224577562

-
5CDS-intronENST00000391875ENST00000479727NVLchr1

224499502

-WDR26chr1

224577562

-
Frame-shiftENST00000281701ENST00000414423NVLchr1

224499502

-WDR26chr1

224577562

-
Frame-shiftENST00000281701ENST00000295024NVLchr1

224499502

-WDR26chr1

224577562

-
5CDS-3UTRENST00000281701ENST00000366852NVLchr1

224499502

-WDR26chr1

224577562

-
5CDS-intronENST00000281701ENST00000479727NVLchr1

224499502

-WDR26chr1

224577562

-
Frame-shiftENST00000469075ENST00000414423NVLchr1

224499502

-WDR26chr1

224577562

-
Frame-shiftENST00000469075ENST00000295024NVLchr1

224499502

-WDR26chr1

224577562

-
5CDS-3UTRENST00000469075ENST00000366852NVLchr1

224499502

-WDR26chr1

224577562

-
5CDS-intronENST00000469075ENST00000479727NVLchr1

224499502

-WDR26chr1

224577562

-
intron-3CDSENST00000482491ENST00000414423NVLchr1

224499502

-WDR26chr1

224577562

-
intron-3CDSENST00000482491ENST00000295024NVLchr1

224499502

-WDR26chr1

224577562

-
intron-3UTRENST00000482491ENST00000366852NVLchr1

224499502

-WDR26chr1

224577562

-
intron-intronENST00000482491ENST00000479727NVLchr1

224499502

-WDR26chr1

224577562

-
intron-3CDSENST00000340871ENST00000414423NVLchr1

224499502

-WDR26chr1

224577562

-
intron-3CDSENST00000340871ENST00000295024NVLchr1

224499502

-WDR26chr1

224577562

-
intron-3UTRENST00000340871ENST00000366852NVLchr1

224499502

-WDR26chr1

224577562

-
intron-intronENST00000340871ENST00000479727NVLchr1

224499502

-WDR26chr1

224577562

-
In-frameENST00000361463ENST00000414423NVLchr1

224499502

-WDR26chr1

224577562

-
In-frameENST00000361463ENST00000295024NVLchr1

224499502

-WDR26chr1

224577562

-
5CDS-3UTRENST00000361463ENST00000366852NVLchr1

224499502

-WDR26chr1

224577562

-
5CDS-intronENST00000361463ENST00000479727NVLchr1

224499502

-WDR26chr1

224577562

-
intron-3CDSENST00000468673ENST00000414423NVLchr1

224499502

-WDR26chr1

224577562

-
intron-3CDSENST00000468673ENST00000295024NVLchr1

224499502

-WDR26chr1

224577562

-
intron-3UTRENST00000468673ENST00000366852NVLchr1

224499502

-WDR26chr1

224577562

-
intron-intronENST00000468673ENST00000479727NVLchr1

224499502

-WDR26chr1

224577562

-

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FusionProtFeatures for NVL_WDR26


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

O15381

WDR26

Q9H7D7

Participates in the assembly of the telomeraseholoenzyme and effecting of telomerase activity via itsinteraction with TERT (PubMed:22226966). May play a role in 60Sribosomal subunit biogenesis (PubMed:15469983, PubMed:16782053).{ECO:0000269|PubMed:15469983, ECO:0000269|PubMed:16782053,ECO:0000269|PubMed:22226966}. G-beta-like protein involved in cell signal transduction(PubMed:15378603, PubMed:19446606, PubMed:22065575,PubMed:23625927, PubMed:27098453, PubMed:26895380). Acts as anegative regulator in MAPK signaling pathway (PubMed:15378603).Functions as a scaffolding protein to promote G beta:gamma-mediated PLCB2 plasma membrane translocation and subsequentactivation in leukocytes (PubMed:22065575, PubMed:23625927). Actsas a negative regulator of the canonical Wnt signaling pathwaythrough preventing ubiquitination of beta-catenin CTNNB1 by thebeta-catenin destruction complex, thus negatively regulatingCTNNB1 degradation (PubMed:27098453). Serves as a scaffold tocoordinate PI3K/AKT pathway-driven cell growth and migration(PubMed:26895380). Protects cells from oxidative stress-inducedapoptosis via the down-regulation of AP-1 transcriptional activityas well as by inhibiting cytochrome c release from mitochondria(PubMed:19446606). Protects also cells by promoting hypoxia-mediated autophagy and mitophagy (By similarity).{ECO:0000250|UniProtKB:F1LTR1, ECO:0000269|PubMed:15378603,ECO:0000269|PubMed:19446606, ECO:0000269|PubMed:23625927,ECO:0000269|PubMed:26895380, ECO:0000269|PubMed:27098453}.

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 NVL_WDR26


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 NVL_WDR26


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
NVLTTF2, CRMP1, OSGEP, SIRT7, CUL3, MOV10, RPL14, NPM1, PRR11, ILF2, HSPB1, IFI16, CEP164, CEP19, UBE2I, RHOA, CLCN2, HNRNPU, RPL10, UBA1, KIF21A, GPATCH4, RRP8, PES1, MAK16, ZNF512, PLEKHO1, FGF8, MECP2, RBM34, DGCR8, ZNF71, RBM4, PPANWDR26RAE1, CUL4B, CUL4A, WDR5, UBC, UBXN7, FAF2, FAF1, USP12, USP46, MAPK6, ARRB2, TSG101, GNB1, GNG2, RANBP10, ZNF131, UBE2O, ZNF687, BARD1, NPM1, SOX2, EGFR, GID8, PNO1, RANBP9, RPS15A, RPS24, RPS26, RPS6, RPS7, RPS8, TSR1, KIAA0368, KCMF1, PLCB2, MAGEA1, TDGF1, MRPL4, RMND5A, PRG2, EPB41L3, NTRK1, CNOT2, KIAA1107, SKI, AXIN1, NFATC2, BMP1, INSL6, PRICKLE3, PIP4K2A, CCDC120, IKZF1, JPH4, PRG3, TIGD5, PIGT, HTRA4, PTPN14, PTPN21, ARMC8, YPEL5, MAEA, UBE2H, HTRA2, RMND5B, GID4, MKLN1, NDUFAF4, NDUFA5, RAB8A, EFHC2, PIK3CB, AKT2, PIK3R1


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 NVL_WDR26


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 NVL_WDR26


check button Diseases associated with fusion partners.
(DisGeNet 4.0)
PartnerGeneDisease IDDisease name# pubmedsSource