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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: 10514

FusionGeneSummary for DPY19L2_NUP107

check button Fusion gene summary
Fusion gene informationFusion gene name: DPY19L2_NUP107
Fusion gene ID: 10514
HgeneTgene
Gene symbol

DPY19L2

NUP107

Gene ID

283417

57122

Gene namedpy-19 like 2nucleoporin 107
SynonymsSPATA34|SPGF9NPHS11|NUP84
Cytomap

12q14.2

12q15

Type of geneprotein-codingprotein-coding
Descriptionprobable C-mannosyltransferase DPY19L2protein dpy-19 homolog 2spermatogenesis associated 34nuclear pore complex protein Nup107nucleoporin 107kDa
Modification date2018052320180523
UniProtAcc

Q6NUT2

P57740

Ensembl transtripts involved in fusion geneENST00000324472, ENST00000413230, 
ENST00000229179, ENST00000378905, 
ENST00000539906, ENST00000401003, 
Fusion gene scores* DoF score2 X 2 X 2=823 X 12 X 9=2484
# samples 226
** MAII scorelog2(2/8*10)=1.32192809488736log2(26/2484*10)=-3.25608164519203
possibly effective Gene in Pan-Cancer Fusion Genes (peGinPCFGs).
DoF>8 and MAII<0
Context

PubMed: DPY19L2 [Title/Abstract] AND NUP107 [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
TgeneNUP107

GO:0006406

mRNA export from nucleus

11684705


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
TCGARVSARCTCGA-DX-AB35-01ADPY19L2chr12

64059615

-NUP107chr12

69124890

+
* 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-shiftENST00000324472ENST00000229179DPY19L2chr12

64059615

-NUP107chr12

69124890

+
5CDS-intronENST00000324472ENST00000378905DPY19L2chr12

64059615

-NUP107chr12

69124890

+
5CDS-intronENST00000324472ENST00000539906DPY19L2chr12

64059615

-NUP107chr12

69124890

+
5CDS-intronENST00000324472ENST00000401003DPY19L2chr12

64059615

-NUP107chr12

69124890

+
intron-3CDSENST00000413230ENST00000229179DPY19L2chr12

64059615

-NUP107chr12

69124890

+
intron-intronENST00000413230ENST00000378905DPY19L2chr12

64059615

-NUP107chr12

69124890

+
intron-intronENST00000413230ENST00000539906DPY19L2chr12

64059615

-NUP107chr12

69124890

+
intron-intronENST00000413230ENST00000401003DPY19L2chr12

64059615

-NUP107chr12

69124890

+

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FusionProtFeatures for DPY19L2_NUP107


check buttonMain function of each fusion partner protein. (from UniProt)
HgeneTgene
DPY19L2

Q6NUT2

NUP107

P57740

Probable C-mannosyltransferase that mediates C-mannosylation of tryptophan residues on target proteins (Bysimilarity). Required during spermatogenesis for sperm headelongation and acrosome formation. {ECO:0000250,ECO:0000269|PubMed:21397063, ECO:0000269|PubMed:21397064}. Plays a role in the nuclear pore complex (NPC) assemblyand/or maintenance (PubMed:12552102, PubMed:15229283). Requiredfor the assembly of peripheral proteins into the NPC(PubMed:15229283, PubMed:12552102). May anchor NUP62 to the NPC(PubMed:15229283). {ECO:0000269|PubMed:12552102,ECO:0000269|PubMed:15229283}.

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 DPY19L2_NUP107


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 DPY19L2_NUP107


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
DPY19L2GUK1NUP107SEH1L, NUP133, NUP85, NUP160, NUP43, NUP37, SEC13, TPR, NUP214, KPNB1, SIRT7, NUP98, WRNIP1, CUL3, CENPF, NUP153, TP53BP1, PNPT1, EIF4B, CORO1B, MYL1, C1QBP, CPSF6, VCP, PYCARD, CUL7, OBSL1, SUZ12, EED, PNKD, NTRK1, IFI16, SYNE1, APC, PRKDC, RRP1B, NALCN, CD1E, ACTBL2, HSP90AB1, XPO1, SENP1, SENP2, AHCTF1, RANGAP1, H2AFV, NUP50, RANBP2, B9D2, ACLY, RCC1, GLE1, ITPR2, KPNA4, NUP88, RAN, UBE2I, SUMO1, AAAS, RAE1, NUP155, NUP93, NUPL1, WDR1, NXF1, IPO7, NUPL2, NUP205, NUP210, NUP188, NUP62, NXT1, SEC61A1, NUP54, TMEM214, SMPD4, NDC1, KRAS, IP6K3, TMEM209, NUP35, RPUSD3, RGPD8, POM121C, FOXA3, FOXI2, FOXK2, FOXL1, FOXP3, FOXQ1, CDC5L, ZNF746, DUSP13, SPAST, UXS1, SIGLECL1, CD70, RAF1, PDHA1, TRIM25, BRCA1


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 DPY19L2_NUP107


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 DPY19L2_NUP107


check button Diseases associated with fusion partners.
(DisGeNet 4.0)
PartnerGeneDisease IDDisease name# pubmedsSource
TgeneNUP107C4225228NEPHROTIC SYNDROME, TYPE 111UNIPROT