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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: 12867

FusionGeneSummary for FAM83D_SF3B3

check button Fusion gene summary
Fusion gene informationFusion gene name: FAM83D_SF3B3
Fusion gene ID: 12867
HgeneTgene
Gene symbol

FAM83D

SF3B3

Gene ID

81610

23450

Gene namefamily with sequence similarity 83 member Dsplicing factor 3b subunit 3
SynonymsC20orf129|CHICA|dJ616B8.3RSE1|SAP130|SF3b130|STAF130
Cytomap

20q11.23

16q22.1

Type of geneprotein-codingprotein-coding
Descriptionprotein FAM83Dspindle protein CHICAsplicing factor 3B subunit 3SAP 130pre-mRNA splicing factor SF3b, 130 kDa subunitspliceosome-associated protein 130
Modification date2018051920180523
UniProtAcc

Q9H4H8

Q15393

Ensembl transtripts involved in fusion geneENST00000217429, ENST00000302516, 
Fusion gene scores* DoF score2 X 2 X 1=43 X 4 X 2=24
# samples 24
** MAII scorelog2(2/4*10)=2.32192809488736log2(4/24*10)=0.736965594166206
effective Gene in Pan-Cancer Fusion Genes (eGinPCFGs).
DoF>8 and MAII>0
Context

PubMed: FAM83D [Title/Abstract] AND SF3B3 [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
HgeneFAM83D

GO:0001837

epithelial to mesenchymal transition

24344117

HgeneFAM83D

GO:0008283

cell proliferation

24344117|25646692

HgeneFAM83D

GO:0016477

cell migration

24344117

HgeneFAM83D

GO:0032006

regulation of TOR signaling

24344117

HgeneFAM83D

GO:0042176

regulation of protein catabolic process

24344117

TgeneSF3B3

GO:0000398

mRNA splicing, via spliceosome

28781166

TgeneSF3B3

GO:0042177

negative regulation of protein catabolic process

23951410


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
TCGARVBRCATCGA-AN-A0FJ-01AFAM83Dchr20

37570769

+SF3B3chr16

70597779

+
* 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-shiftENST00000217429ENST00000302516FAM83Dchr20

37570769

+SF3B3chr16

70597779

+

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FusionProtFeatures for FAM83D_SF3B3


check buttonMain function of each fusion partner protein. (from UniProt)
HgeneTgene
FAM83D

Q9H4H8

SF3B3

Q15393

Involved in pre-mRNA splicing as a component of thesplicing factor SF3B complex, a constituent of the spliceosome(PubMed:10490618, PubMed:10882114, PubMed:27720643,PubMed:28781166). SF3B complex is required for 'A' complexassembly formed by the stable binding of U2 snRNP to thebranchpoint sequence (BPS) in pre-mRNA. Sequence independentbinding of SF3A/SF3B complex upstream of the branch site isessential, it may anchor U2 snRNP to the pre-mRNA(PubMed:12234937). May also be involved in the assembly of the 'E'complex (PubMed:10882114). Belongs also to the minor U12-dependentspliceosome, which is involved in the splicing of rare class ofnuclear pre-mRNA intron (PubMed:15146077).{ECO:0000269|PubMed:10490618, ECO:0000269|PubMed:10882114,ECO:0000269|PubMed:12234937, ECO:0000269|PubMed:15146077,ECO:0000269|PubMed:27720643, ECO:0000269|PubMed:28781166}.

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 FAM83D_SF3B3


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 FAM83D_SF3B3


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
FAM83DCSNK1E, GSK3B, DYNC1I1, GADD45A, PRMT1, CSNK1A1, TRAK2, PSMC3, CRYAB, CEP170, DCTN1, BACH1, KRAS, DYNLL1, SEC16A, FBXW7, HMMR, CCDC40, GMNN, BBS7, NMD3, POTEB3, CSNK1D, NPAS1SF3B3SMNDC1, CFLAR, TNFRSF10D, RNPS1, RNU11, NCOR1, SF3B2, SF3B1, SF3A2, SUPT3H, TAF9, HGS, TCEA1, SRRM1, SRRM2, KAT2A, HDAC5, TOP1, YWHAG, SMAD5, KLF10, OSGEP, RUFY2, RAD9A, ZNF579, NAGK, SMARCAD1, SREK1, TAF10, ARRB2, CUL3, CUL2, CDK2, CUL1, COPS5, CAND1, SF3A1, SNRPD1, HNRNPK, SNRPD2, SF3A3, SNRPA1, SF3B4, SF3B5, SF3B6, PHF5A, SNRNP200, PRPF8, SNRPB2, SRSF1, HNRNPR, TCERG1, EFTUD2, PRPF6, RBMX, YBX1, SNRPA, SRSF7, HNRNPM, U2AF1, U2AF2, SRSF2, DDX5, PRPF31, SFPQ, SMC1A, PRPF19, SART1, SMU1, LMNA, TUBB, WDR18, STOML2, CCT2, TPBG, LAMP2, TRA2A, TXNRD1, ZC3H18, TJAP1, UBE3A, SPDL1, UTP14A, VTN, VPS33B, AGMAT, THRAP3, MTHFD1, TMOD2, STOM, TRIM55, SSR3, MAGOH, EIF4A3, PPIL1, HSPB1, TOE1, HSP90AA1, IFIT3, CD81, IGSF8, SKP1, SKP2, CUL4A, EPS8, RBM6, FBXO6, PRPF40A, WBP4, APBB1, WWOX, RPA3, RPA2, RPA1, ERG, LGR4, NUDCD3, HUWE1, FUS, MDM2, CCDC101, CUL7, OBSL1, CCDC8, EZH2, SUZ12, EED, RNF2, USP7, UNK, BCAS2, CCAR1, CCAR2, DCTN1, ISY1-RAB43, ISY1, LUC7L, PRPF3, PRPF4, CCDC97, CDC40, CDC5L, COPA, COPE, COPG1, DHX15, EIF4G1, ELP4, KPNB1, LMNB1, LSM4, LUC7L2, PLRG1, PSME3, RPL18A, SRRT, USP10, XAB2, SMC3, SNRPD3, SPTAN1, SSSCA1, SYNCRIP, RNU12, NTRK1, SCARNA22, TAF4, HIST1H3E, MCM5, SNW1, AIRE, ZNF746, FLCN, SNRPE, PLK1, CYLD, CD2BP2, TRIM25, BRCA1, YAP1


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 FAM83D_SF3B3


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 FAM83D_SF3B3


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