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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: 25177

FusionGeneSummary for NUP107_SHD

check button Fusion gene summary
Fusion gene informationFusion gene name: NUP107_SHD
Fusion gene ID: 25177
HgeneTgene
Gene symbol

NUP107

SHD

Gene ID

57122

56961

Gene namenucleoporin 107Src homology 2 domain containing transforming protein D
SynonymsNPHS11|NUP84-
Cytomap

12q15

19p13.3

Type of geneprotein-codingprotein-coding
Descriptionnuclear pore complex protein Nup107nucleoporin 107kDaSH2 domain-containing adapter protein Dsrc homology 2 domain-containing transforming protein D
Modification date2018052320180523
UniProtAcc

P57740

Q96IW2

Ensembl transtripts involved in fusion geneENST00000229179, ENST00000378905, 
ENST00000539906, ENST00000401003, 
ENST00000543264, ENST00000599689, 
ENST00000600475, 
Fusion gene scores* DoF score5 X 4 X 4=802 X 2 X 1=4
# samples 52
** MAII scorelog2(5/80*10)=-0.678071905112638
possibly effective Gene in Pan-Cancer Fusion Genes (peGinPCFGs).
DoF>8 and MAII<0
log2(2/4*10)=2.32192809488736
Context

PubMed: NUP107 [Title/Abstract] AND SHD [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
HgeneNUP107

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
TCGARVLUADTCGA-55-8506-01ANUP107chr12

69109520

+SHDchr19

4290444

+
* 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-shiftENST00000229179ENST00000543264NUP107chr12

69109520

+SHDchr19

4290444

+
Frame-shiftENST00000229179ENST00000599689NUP107chr12

69109520

+SHDchr19

4290444

+
5CDS-intronENST00000229179ENST00000600475NUP107chr12

69109520

+SHDchr19

4290444

+
Frame-shiftENST00000378905ENST00000543264NUP107chr12

69109520

+SHDchr19

4290444

+
Frame-shiftENST00000378905ENST00000599689NUP107chr12

69109520

+SHDchr19

4290444

+
5CDS-intronENST00000378905ENST00000600475NUP107chr12

69109520

+SHDchr19

4290444

+
Frame-shiftENST00000539906ENST00000543264NUP107chr12

69109520

+SHDchr19

4290444

+
Frame-shiftENST00000539906ENST00000599689NUP107chr12

69109520

+SHDchr19

4290444

+
5CDS-intronENST00000539906ENST00000600475NUP107chr12

69109520

+SHDchr19

4290444

+
intron-3CDSENST00000401003ENST00000543264NUP107chr12

69109520

+SHDchr19

4290444

+
intron-3CDSENST00000401003ENST00000599689NUP107chr12

69109520

+SHDchr19

4290444

+
intron-intronENST00000401003ENST00000600475NUP107chr12

69109520

+SHDchr19

4290444

+

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FusionProtFeatures for NUP107_SHD


check buttonMain function of each fusion partner protein. (from UniProt)
HgeneTgene
NUP107

P57740

SHD

Q96IW2

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}. May function as an adapter protein. {ECO:0000250}.

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 NUP107_SHD


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 NUP107_SHD


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
NUP107SEH1L, 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, BRCA1SHDABL1, CAPN10, PSG11, KRTCAP2, OLIG1, OSBPL6, BECN1, MRPS22


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 NUP107_SHD


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 NUP107_SHD


check button Diseases associated with fusion partners.
(DisGeNet 4.0)
PartnerGeneDisease IDDisease name# pubmedsSource
HgeneNUP107C4225228NEPHROTIC SYNDROME, TYPE 111UNIPROT