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Center for Computational Systems Medicine level1
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Fusion Gene Summary

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Fusion Gene Sample Information

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Fusion ORF Analysis

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Fusion Amino Acid Sequences

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Fusion Protein Functional Features

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Fusion Protein-Protein Interaction

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Related drugs with this fusion protein

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Related disease with this fusion protein

Fusion Protein:UBE2D2-SND1

Fusion Protein Summary

check button Fusion gene summary
Fusion partner gene informationFusion gene name: UBE2D2-SND1
FusionPDB ID: 96022
FusionGDB2.0 ID: 96022
HgeneTgene
Gene symbol

UBE2D2

SND1

Gene ID

7322

27044

Gene nameubiquitin conjugating enzyme E2 D2staphylococcal nuclease and tudor domain containing 1
SynonymsE2(17)KB2|PUBC1|UBC4|UBC4/5|UBCH4|UBCH5BTDRD11|Tudor-SN|p100
Cytomap

5q31.2

7q32.1

Type of geneprotein-codingprotein-coding
Descriptionubiquitin-conjugating enzyme E2 D2(E3-independent) E2 ubiquitin-conjugating enzyme D2E2 ubiquitin-conjugating enzyme D2p53-regulated ubiquitin-conjugating enzyme 1ubiquitin carrier protein D2ubiquitin conjugating enzyme E2D 2ubiquitin-conjugating enstaphylococcal nuclease domain-containing protein 1EBNA2 coactivator p100testis tissue sperm-binding protein Li 82Ptudor domain-containing protein 11
Modification date2020031320200313
UniProtAcc.

Q7KZF4

Ensembl transtripts involved in fusion geneENST idsENST00000398733, ENST00000253815, 
ENST00000505548, ENST00000511725, 
ENST00000467238, ENST00000354725, 
Fusion gene scores for assessment (based on all fusion genes of FusionGDB 2.0)* DoF score18 X 9 X 11=178229 X 24 X 11=7656
# samples 2333
** MAII scorelog2(23/1782*10)=-2.95379157057755
possibly effective Gene in Pan-Cancer Fusion Genes (peGinPCFGs).
DoF>8 and MAII<0
log2(33/7656*10)=-4.53605290024021
possibly effective Gene in Pan-Cancer Fusion Genes (peGinPCFGs).
DoF>8 and MAII<0
Context (manual curation of fusion genes in FusionPDB)

PubMed: UBE2D2 [Title/Abstract] AND SND1 [Title/Abstract] AND fusion [Title/Abstract]

Most frequent breakpoint (based on all fusion genes of FusionGDB 2.0)UBE2D2(138941400)-SND1(127714554), # samples:3
Anticipated loss of major functional domain due to fusion event.UBE2D2-SND1 seems lost the major protein functional domain in Hgene partner, which is a CGC by not retaining the major functional domain in the partially deleted in-frame ORF.
UBE2D2-SND1 seems lost the major protein functional domain in Hgene partner, which is a CGC by not retaining the major functional domain in the partially deleted in-frame ORF.
UBE2D2-SND1 seems lost the major protein functional domain in Hgene partner, which is a essential gene by not retaining the major functional domain in the partially deleted in-frame ORF.
UBE2D2-SND1 seems lost the major protein functional domain in Hgene partner, which is a essential gene by not retaining the major functional domain in the partially deleted in-frame ORF.
* 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
HgeneUBE2D2

GO:0000209

protein polyubiquitination

15247280

HgeneUBE2D2

GO:0016567

protein ubiquitination

9990509|14593114

HgeneUBE2D2

GO:0051865

protein autoubiquitination

21068390

HgeneUBE2D2

GO:0070936

protein K48-linked ubiquitination

20061386

TgeneSND1

GO:0010587

miRNA catabolic process

28546213


check buttonFusion gene breakpoints across UBE2D2 (5'-gene)
* Click on the image to open the UCSC genome browser with custom track showing this image in a new window.
all structure

check buttonFusion gene breakpoints across SND1 (3'-gene)
* Click on the image to open the UCSC genome browser with custom track showing this image in a new window.
all structure


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Fusion Gene Sample Information

check buttonFusion gene information from FusionGDB2.0.
check button Fusion gene information from two resources (ChiTars 5.0 and ChimerDB 4.0)
* 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.
SourceDiseaseSampleHgeneHchrHbpHstrandTgeneTchrTbpTstrand
ChimerDB4LUADTCGA-95-7562-01AUBE2D2chr5

138941400

-SND1chr7

127714554

+
ChimerDB4LUADTCGA-95-7562-01AUBE2D2chr5

138941400

+SND1chr7

127714554

+


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Fusion ORF Analysis


check buttonFusion information from ORFfinder translation from full-length transcript sequence from FusionPDB.
HenstTenstHgeneHchrHbpHstrandTgeneTchrTbpTstrandSeq length
(transcript)
BP loci
(transcript)
Predicted start
(transcript)
Predicted stop
(transcript)
Seq length
(amino acids)
ENST00000398733UBE2D2chr5138941400+ENST00000354725SND1chr7127714554+21536505211603360

check buttonDeepORF prediction of the coding potential based on the fusion transcript sequence of in-frame fusion genes. DeepORF is a coding potential classifier based on convolutional neural network by comparing the real Ribo-seq data. If the no-coding score < 0.5 and coding score > 0.5, then the in-frame fusion transcript is predicted as being likely translated.
HenstTenstHgeneHchrHbpHstrandTgeneTchrTbpTstrandNo-coding scoreCoding score
ENST00000398733ENST00000354725UBE2D2chr5138941400+SND1chr7127714554+0.0022887260.9977113

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Fusion Amino Acid Sequences


check button For individual full-length fusion transcript sequence from FusionPDB, we ran ORFfinder and chose the longest ORF among the all predicted ones.
>FusionGDB ID_FusionGDB isoform ID_FGname_Hgene_Hchr_Hbp_Henst_Tgene_Tchr_Tbp_Tenst_length(fusion AA) seq_BP

>96022_96022_1_UBE2D2-SND1_UBE2D2_chr5_138941400_ENST00000398733_SND1_chr7_127714554_ENST00000354725_length(amino acids)=360AA_BP=43
MPTEIAEAASGSLAPSPSLPRPRPRPGGRRHPPPTMALKRIHKVEVEVESMDKAGNFIGWLHIDGANLSVLLVEHALSKVHFTAERSSYY
KSLLSAEEAAKQKKEKVWAHYEEQPVEEVMPVLEEKERSASYKPVFVTEITDDLHFYVQDVETGTQLEKLMENMRNDIASHPPVEGSYAP
RRGEFCIAKFVDGEWYRARVEKVESPAKIHVFYIDYGNREVLPSTRLGTLSPAFSTRVLPAQATEYAFAFIQVPQDDDARTDAVDSVVRD
IQNTQCLLNVEHLSAGCPHVTLQFADSKGDVGLGLVKEGLVMVEVRKEKQFQKVITEYLNAQESAKSARLNLWRYGDFRADDADEFGYSR

--------------------------------------------------------------

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Fusion Protein Functional Features


check button Four levels of functional features of fusion genes
Go to FGviewer search page for the most frequent breakpoint (https://ccsmweb.uth.edu/FGviewer/chr5:138941400/chr7:127714554)
- FGviewer provides the online visualization of the retention search of the protein functional features across DNA, RNA, protein, and pathological levels.
- How to search
1. Put your fusion gene symbol.
2. Press the tab key until there will be shown the breakpoint information filled.
4. Go down and press 'Search' tab twice.
4. Go down to have the hyperlink of the search result.
5. Click the hyperlink.
6. See the FGviewer result for your fusion gene.
FGviewer

check buttonMain function of each fusion partner protein. (from UniProt)
HgeneTgene
.SND1

Q7KZF4

FUNCTION: Might normally function as a transcriptional repressor. EWS-fusion-proteins (EFPS) may play a role in the tumorigenic process. They may disturb gene expression by mimicking, or interfering with the normal function of CTD-POLII within the transcription initiation complex. They may also contribute to an aberrant activation of the fusion protein target genes.FUNCTION: Endonuclease that mediates miRNA decay of both protein-free and AGO2-loaded miRNAs (PubMed:28546213, PubMed:18453631). As part of its function in miRNA decay, regulates mRNAs involved in G1-to-S phase transition (PubMed:28546213). Functions as a bridging factor between STAT6 and the basal transcription factor (PubMed:12234934). Plays a role in PIM1 regulation of MYB activity (PubMed:9809063). Functions as a transcriptional coactivator for STAT5 (By similarity). {ECO:0000250|UniProtKB:Q78PY7, ECO:0000269|PubMed:12234934, ECO:0000269|PubMed:18453631, ECO:0000269|PubMed:28546213, ECO:0000269|PubMed:9809063}.; FUNCTION: (Microbial infection) Functions as a transcriptional coactivator for the Epstein-Barr virus nuclear antigen 2 (EBNA2). {ECO:0000269|PubMed:7651391}.

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.
- Retained protein feature among the 13 regional features.
PartnerGeneHbpTbpENSTStrandBPexonTotalExonProtein feature loci*BPlociTotalLenProtein featureProtein feature note
TgeneSND1chr5:138941400chr7:127714554ENST000003547251524729_787593.0911.0DomainTudor

- Not-retained protein feature among the 13 regional features.
PartnerGeneHbpTbpENSTStrandBPexonTotalExonProtein feature loci*BPlociTotalLenProtein featureProtein feature note
HgeneUBE2D2chr5:138941400chr7:127714554ENST00000253815+181_1470119.0DomainUBC core
HgeneUBE2D2chr5:138941400chr7:127714554ENST00000398733+171_1478.0148.0DomainUBC core
HgeneUBE2D2chr5:138941400chr7:127714554ENST00000505548+171_1470119.0DomainUBC core
HgeneUBE2D2chr5:138941400chr7:127714554ENST00000511725+171_1470119.0DomainUBC core
TgeneSND1chr5:138941400chr7:127714554ENST00000354725152418_166593.0911.0DomainTNase-like 1
TgeneSND1chr5:138941400chr7:127714554ENST000003547251524193_328593.0911.0DomainTNase-like 2
TgeneSND1chr5:138941400chr7:127714554ENST000003547251524341_496593.0911.0DomainTNase-like 3
TgeneSND1chr5:138941400chr7:127714554ENST000003547251524525_660593.0911.0DomainTNase-like 4
TgeneSND1chr5:138941400chr7:127714554ENST000003547251524321_325593.0911.0MotifNuclear localization signal
TgeneSND1chr5:138941400chr7:127714554ENST000003547251524388_392593.0911.0MotifNuclear localization signal


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Fusion Protein-Protein Interaction


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 from validated records (BIOGRID-3.4.160)
GenePPI interactors
SND1IKBKE, SNW1, RBPJ, GTF2E2, GTF2E1, MYB, PIM1, STAT6, POLR2A, USP22, PDPK1, PRKAA1, UBA5, LZTR1, DHX9, CREBBP, RBM39, SIRT7, HHV8GK18_gp81, CUL3, CDK2, CAND1, APP, RPS3, HNRNPM, TOMM22, RPL19, MYBBP1A, SMNDC1, RPS20, NENF, RPL4, VDAC2, ILF2, SRSF3, HNRNPU, RPN1, HNRNPR, SSR3, FN1, VCAM1, CSNK2A1, ITGA4, G3BP1, PRPF8, RNU1-1, RNU2-1, RNU4-1, RNU6-1, RNU5A-1, MAK, TARDBP, EIF3CL, RPS11, RPS2, RPS6, RPS9, DDX3X, RPL23A, RPL35, RPS16, RPS26, RPS27, RPS3A, SHFM1, LIN28A, HUWE1, RAPGEF2, MDM2, CUL7, OBSL1, CCDC8, UBE2I, ESR1, MMP28, TDRD3, TXNDC5, NTRK1, NPM1, RPL10, CNOT1, Eif3a, Pabpc1, Rpl35, Srp72, Rrbp1, MCM2, U2AF2, CDH1, PTP4A1, MTDH, PA2G4, TRAP1, ANXA5, SNRPB2, EIF5B, GPI, IDH2, PDIA3, UBE2N, MRPL12, CRNN, ZNF207, CPNE3, CS, PYGL, SF3A3, DNAJC8, PLS3, CPSF6, NANS, SF3A1, ECHS1, SRP68, MYL12B, AIMP1, CYLD, DLD, DLST, PDHA1, SOD1, TRIM25, BRCA1, YAP1, EFTUD2, AAR2, PIH1D1, CHD3, ESR2, HEXIM1, AGR2, RECQL4, WWP1, MYC, CANX, GRWD1, KIAA1429, ATG16L1, NR2C2, AGRN, BMH2, BMH1, BRF1, AASS, P4HA1, HSP90AA1, HSP90AB1, LRPPRC, HADHA, ATP5C1, SHMT2, MCFD2, ATP5F1, VCP, CTNNB1, BCAP31, DLAT, EPRS, ILF3, PARP1, SFPQ, ALDH16A1, BCL2L13, CCT7, CORO1C, GFM1, PNPT1, SQSTM1, MAB21L2, SNRNP70, GSK3B, ANO7, BIRC3, STAU1, LMBR1L, NFX1, WWP2, Hsp22, TRIM28, PLEKHA4, PINK1, HCVgp1, ZC3H18, FGFR1, EMC4, HNRNPC, M, nsp4, nsp6, nsp8, ORF7b, CAPRIN1, LARP4B, MEX3B, SYNCRIP, TOP3B, UNK, USP10, SDCCAG3, CIT, ANLN, PTGER4, KIF14, FKBP8, PTPN1, ORF9b, LRRC59, SUMO2, NDN, HULC, NUPR1, BRD4, Apc2, LGALS9, IFI16, BKRF1, ASXL1, DNAJC1, DNAJC25, SEC63, H2AFX, TFDP1, MAX, LINC00624, CD274, ISG15, UFL1, DDRGK1, TP53, CKAP4, ELOVL5, EMD, GORASP1, MAPRE1, METTL7A, RPS24, SEC61B, SEC62, SERBP1, SSR1, STIM1, STX4, TMPO, FZR1, HOXA1, NAA40, BGLT3, PSMC3, ARFGAP1, PRPS2, SPINT2, FAM221B, BDH2, SYT6, EP300, CTIF, RCHY1, CCNF, MAP1LC3B, SLFN11, PDE4B, SIRT6,


check button Protein-protein interactors based on sequence similarity (STRING)
GeneSTRING network
UBE2D2
SND1all structure


check button - Retained interactions in fusion protein (protein functional feature from UniProt).
PartnerGeneHbpTbpENSTStrandBPexonTotalExonProtein feature loci*BPlociTotalLenStill interaction with


check button - Lost interactions due to fusion (protein functional feature from UniProt).
PartnerGeneHbpTbpENSTStrandBPexonTotalExonProtein feature loci*BPlociTotalLenInteraction lost with


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Related Drugs to UBE2D2-SND1


check button Drugs used for this fusion-positive patient.
(Manual curation of PubMed, 04-30-2022 + MyCancerGenome)
HgeneTgeneDrugSourcePMID

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Related Diseases to UBE2D2-SND1


check button Diseases that have this fusion gene.
(Manual curation of PubMed, 04-30-2022 + MyCancerGenome)
HgeneTgeneDiseaseSourcePMID

check button Diseases associated with fusion partners.
(DisGeNet 4.0)
PartnerGeneDisease IDDisease name# pubmedsSource
TgeneSND1C0004352Autistic Disorder1CTD_human
TgeneSND1C0024121Lung Neoplasms1CTD_human
TgeneSND1C0242379Malignant neoplasm of lung1CTD_human