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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: 35131

FusionGeneSummary for SNHG3_CUL2

check button Fusion gene summary
Fusion gene informationFusion gene name: SNHG3_CUL2
Fusion gene ID: 35131
HgeneTgene
Gene symbol

SNHG3

CUL2

Gene ID

8420

8453

Gene namesmall nucleolar RNA host gene 3cullin 2
SynonymsNCRNA00014|RNU17C|RNU17D|U17HG|U17HG-A|U17HG-AB-
Cytomap

1p35.3

10p11.21

Type of genencRNAprotein-coding
DescriptionU17 small nucleolar RNA hostsmall nucleolar RNA host gene (non-protein coding) 3small nucleolar RNA host gene 3 (non-protein coding)cullin-2CUL-2testis secretory sperm-binding protein Li 238E
Modification date2018051920180523
UniProtAcc

Q13617

Ensembl transtripts involved in fusion geneENST00000364938, ENST00000374746, 
ENST00000374748, ENST00000374749, 
ENST00000374751, ENST00000602371, 
ENST00000374742, ENST00000537177, 
ENST00000478044, 
Fusion gene scores* DoF score15 X 7 X 4=4204 X 4 X 4=64
# samples 155
** MAII scorelog2(15/420*10)=-1.48542682717024
possibly effective Gene in Pan-Cancer Fusion Genes (peGinPCFGs).
DoF>8 and MAII<0
log2(5/64*10)=-0.356143810225275
possibly effective Gene in Pan-Cancer Fusion Genes (peGinPCFGs).
DoF>8 and MAII<0
Context

PubMed: SNHG3 [Title/Abstract] AND CUL2 [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
ChiTaRS3.1BG256861SNHG3chr1

28834672

+CUL2chr10

35360268

-
* 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-3CDSENST00000364938ENST00000374746SNHG3chr1

28834672

+CUL2chr10

35360268

-
intron-5UTRENST00000364938ENST00000374748SNHG3chr1

28834672

+CUL2chr10

35360268

-
intron-5UTRENST00000364938ENST00000374749SNHG3chr1

28834672

+CUL2chr10

35360268

-
intron-5UTRENST00000364938ENST00000374751SNHG3chr1

28834672

+CUL2chr10

35360268

-
intron-5UTRENST00000364938ENST00000602371SNHG3chr1

28834672

+CUL2chr10

35360268

-
intron-5UTRENST00000364938ENST00000374742SNHG3chr1

28834672

+CUL2chr10

35360268

-
intron-5UTRENST00000364938ENST00000537177SNHG3chr1

28834672

+CUL2chr10

35360268

-
intron-5UTRENST00000364938ENST00000478044SNHG3chr1

28834672

+CUL2chr10

35360268

-

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FusionProtFeatures for SNHG3_CUL2


check buttonMain function of each fusion partner protein. (from UniProt)
HgeneTgene
SNHG3

CUL2

Q13617

Lectin that binds to various sugars: galactose > mannose= fucose > N-acetylglucosamine > N-acetylgalactosamine(PubMed:10224141). Acts as a chemoattractant, probably involved inthe regulation of cell migration (PubMed:28301481).{ECO:0000269|PubMed:10224141, ECO:0000269|PubMed:28301481}. Core component of multiple cullin-RING-based ECS(ElonginB/C-CUL2/5-SOCS-box protein) E3 ubiquitin-protein ligasecomplexes, which mediate the ubiquitination of target proteins.ECS complexes and ARIH1 collaborate in tandem to mediateubiquitination of target proteins (PubMed:27565346). May serve asa rigid scaffold in the complex and may contribute to catalysisthrough positioning of the substrate and the ubiquitin-conjugatingenzyme. The E3 ubiquitin-protein ligase activity of the complex isdependent on the neddylation of the cullin subunit and isinhibited by the association of the deneddylated cullin subunitwith TIP120A/CAND1. The functional specificity of the ECS complexdepends on the substrate recognition component. ECS(VHL) mediatesthe ubiquitination of hypoxia-inducible factor (HIF).{ECO:0000269|PubMed:10973499, ECO:0000269|PubMed:11384984,ECO:0000269|PubMed:27565346, ECO:0000269|PubMed:9122164}.

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 SNHG3_CUL2


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 SNHG3_CUL2


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
SNHG3UTP23, TRIM25CUL2RNF7, VHL, P4HB, CAB39, TFE3, TIMM13, STOM, RPL35P5, PFKFB3, RNMTL1, KCTD5, CMBL, DLG3, CAND1, RBX1, TCEB2, TCEB1, DCUN1D1, SAP130, ASB4, COPS5, COPS6, TCEAL1, HIF1A, COMMD1, KLHDC10, SH3GLB1, COPS3, KEAP1, ARID1B, ARID1A, COPS2, UBE2D1, RELA, DNMT3B, ARNT, NSFL1C, FAF2, FAF1, UBXN7, UBXN1, VCP, KAT2A, ADRB2, ASB2, MED8, FBXW8, GLMN, PFDN5, SKP2, SQSTM1, NEDD8, PRAME, BCL2L11, TOP2A, ZYG11B, ZER1, FEM1B, APPBP2, KLHDC2, KLHDC3, PCMTD2, CUL5, ABCF1, ACLY, ACTA2, ACTB, ACTBL2, AGL, AIFM1, AKAP8L, FBF1, ALDOA, ANKRD39, ANXA2, ANXA2P2, APOD, ASPRV1, BAG4, BOLA2, BOLA2B, BRAP, BTG3, EDRF1, C11orf70, C14orf166, C1QBP, RTCB, VWA7, YAE1D1, DFFB, CARM1, CASP14, CDKN2A, CEP152, CIRBP, CLTC, COPS4, COPS7A, COPS7B, COPS8, LUC7L3, YBX3, CSTA, CTPS1, CTSD, CUL4B, DAZAP1, DCD, DDX1, DDX17, DDX56, DDX3X, DDX5, DERL2, DHX15, DHX9, DNAJA1, DNAJB6, DNAJC10, DSG1, DSP, EEF1A1, EEF1A2, EEF1B2, EEF1D, EEF1G, EGFLAM, AGO2, EIF5A, ELAVL1, EMD, ENO1, ENO2, EWSR1, FAM103A1, FAM98A, FEM1A, FEM1C, FLG, FLG2, FUS, GAPDH, GDPD3, GLDC, GPS1, GRSF1, GSTP1, HIST1H1C, HIST2H2BE, HNRNPA0, HNRNPA1, HNRNPA2B1, HNRNPA3, HNRNPAB, HNRNPC, HNRNPCL1, HNRNPD, HNRNPF, HNRNPH1, HNRNPH3, HNRNPK, HNRNPM, HNRNPR, HNRNPU, HNRNPUL1, HNRNPDL, HRNR, HSP90AA1, HSP90AA2P, HSP90AB1, HSP90AB2P, HSP90B1, HSPA1A, HSPA1B, HSPA1L, HSPA5, HSPA7, HSPA8, HSPA9, TRMT112, HSPD1, IGF2BP1, IGKV4-1, ILF2, ILF3, IRS4, JUP, KDELC1, KHSRP, KLC3, PPP1R21, KRT1, KRT10, KRT13, KRT14, KRT16, KRT2, KRT24, KRT5, KRT6A, KRT6C, KRT71, KRT75, KRT76, KRT78, KRT9, LARP1, LGALS3BP, IGHV3OR15-7, LOXL1, LRRC14, MCM3, MLPH, MORC2, MRTO4, MTHFD1, MTHFSD, MYEOV2, NAP1L1, NCL, NFRKB, NKAPL, NONO, NPM1, NUCB2, NUDT1, NUP214, NUP88, PABPC1, PABPC4, PABPN1, PARP14, PCBP1, PCBP2, PCMT1, PCNA, PDCD6, PEPD, PHGDH, PKM, PLOD1, POLR2A, POP7, PPFIA1, LRR1, PRDX1, PRDX2, PRDX3, PRDX4, PRMT1, PRPF39, PSMD4, PTOV1, QPCT, RANBP2, RBM14, RBM4, RBM3, RCBTB1, RNF187, RNMT, RNPS1, RPL10P16, RPL11, RPL12, RPL13, RPL13P12, RPL14, RPL15, RPL18, RPL19, RPL21P19, RPL21, RPL21P16, RPL22, RPL23, RPL23A, RPL24, RPL27, RPL27A, RPL28, RPL29P11, RPL29P30, RPL3, RPL31, RPL36, HNRNPH2, RPL36AP37, RPL38, RPL4, RPL5, RPL6, RPL7, RPL7P32, RPL7AP9, RPL7AP27, RPL8, RPL9, RPLP0, RPLP1, RPLP2, RPS13, RPS14, RPS15A, RPS16, RPS18, RPS2, RPS20, RPS23, RPS24, RPS25, RPS27, RPS3, RPS3A, RPS4X, RPS6, RPS8, RPS9, RPSAP12, RPSAP55, S100A9, SAMHD1, SDHA, SDHB, SEC23A, SERPINB12, SERPINB3, SERPINB4, SF3B3, SRSF1, SRSF2, SRSF3, SRSF6, SRSF7, SLC16A1, SLC25A3, SLC25A5, SMAD6, SMC3, SMPD4, SNRNP200, SNRNP70, SNRPA, SNRPB, SNRPC, SNRPD1, SNRPD2, SNRPD3, SNRPE, SNRPF, SNW1, SSB, SYNCRIP, TAF15, TBC1D15, TBC1D17, TBC1D4, TCEB1P3, TFG, ALYREF, TIA1, TIAL1, TMCC3, TNRC6B, TRA2B, TRIM28, TRIM44, TRIM9, TTN, TUBA1C, TUBA4A, TUBB, TUBB1, TUBB2A, TUBB4B, TUFM, TXN, UBC, UBE2M, UBR1, USP25, WDR77, YBX1, YWHAQ, YWHAZ, ZCCHC11, ZRANB3, HIST1H4J, HIST4H4, HIST1H4E, HIST1H4H, HIST1H4K, HIST2H4A, HIST1H4D, HIST1H4F, HIST2H4B, HIST1H4C, HIST1H4B, HIST1H4I, HIST1H4L, HIST1H4A, PTPN14, LAGE3, OSGEP, CISH, GNB2L1, KLF4, MKNK2, RFWD2, DCUN1D2, DCUN1D3, DCUN1D4, DCUN1D5, PLK1, FBXL2, CCDC22, AR, DLC1, ATP6V1B2, CTNNA1, DPYSL3, MSH2, NARS, ST13, XRCC5, XRCC6, KPNB1, NDRG1, CSNK1E, SHFM1, SHMT2, MOV10, NXF1, CDC34, SENP8, ARIH1, MRM1, SKAP1, TSGA10IP, RHOB, UNK, ATP6V1D, CIAPIN1, CUL3, NTRK1, TARDBP, EPOR, SLBP, PYCARD, OXT, PRAMEF17, IKZF1, AVP, SYCE3, RGS20, 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 SNHG3_CUL2


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 SNHG3_CUL2


check button Diseases associated with fusion partners.
(DisGeNet 4.0)
PartnerGeneDisease IDDisease name# pubmedsSource
TgeneCUL2C0021390Inflammatory Bowel Diseases1CTD_human