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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: 33463

FusionGeneSummary for SF3B3_CDH3

check button Fusion gene summary
Fusion gene informationFusion gene name: SF3B3_CDH3
Fusion gene ID: 33463
HgeneTgene
Gene symbol

SF3B3

CDH3

Gene ID

23450

1013

Gene namesplicing factor 3b subunit 3cadherin 15
SynonymsRSE1|SAP130|SF3b130|STAF130CDH14|CDH3|CDHM|MCAD|MRD3
Cytomap

16q22.1

16q24.3

Type of geneprotein-codingprotein-coding
Descriptionsplicing factor 3B subunit 3SAP 130pre-mRNA splicing factor SF3b, 130 kDa subunitspliceosome-associated protein 130cadherin-15cadherin 15, type 1, M-cadherin (myotubule)cadherin-14cadherin-3muscle-cadherin
Modification date2018052320180523
UniProtAcc

Q15393

P22223

Ensembl transtripts involved in fusion geneENST00000302516, ENST00000264012, 
ENST00000429102, ENST00000581171, 
ENST00000569117, 
Fusion gene scores* DoF score10 X 10 X 7=7006 X 6 X 4=144
# samples 126
** MAII scorelog2(12/700*10)=-2.54432051622381
possibly effective Gene in Pan-Cancer Fusion Genes (peGinPCFGs).
DoF>8 and MAII<0
log2(6/144*10)=-1.26303440583379
possibly effective Gene in Pan-Cancer Fusion Genes (peGinPCFGs).
DoF>8 and MAII<0
Context

PubMed: SF3B3 [Title/Abstract] AND CDH3 [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
HgeneSF3B3

GO:0000398

mRNA splicing, via spliceosome

28781166

HgeneSF3B3

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
TCGALDLUADTCGA-44-7667-01ASF3B3chr16

70578436

+CDH3chr16

89245824

+
* 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
5CDS-intronENST00000302516ENST00000264012SF3B3chr16

70578436

+CDH3chr16

89245824

+
5CDS-intronENST00000302516ENST00000429102SF3B3chr16

70578436

+CDH3chr16

89245824

+
5CDS-intronENST00000302516ENST00000581171SF3B3chr16

70578436

+CDH3chr16

89245824

+
5CDS-intronENST00000302516ENST00000569117SF3B3chr16

70578436

+CDH3chr16

89245824

+

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FusionProtFeatures for SF3B3_CDH3


check buttonMain function of each fusion partner protein. (from UniProt)
HgeneTgene
SF3B3

Q15393

CDH3

P22223

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}. Cadherins are calcium-dependent cell adhesion proteins.They preferentially interact with themselves in a homophilicmanner in connecting cells; cadherins may thus contribute to thesorting of heterogeneous cell types.

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 SF3B3_CDH3


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 SF3B3_CDH3


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
SF3B3SMNDC1, 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, YAP1CDH3CDH1, CDH3, CTNNA1, CTNNB1, JUP, CTNND1, AP2M1, CTNNA3, PCDHGB1


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 SF3B3_CDH3


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 SF3B3_CDH3


check button Diseases associated with fusion partners.
(DisGeNet 4.0)
PartnerGeneDisease IDDisease name# pubmedsSource
TgeneCDH3C0009324Ulcerative Colitis1CTD_human
TgeneCDH3C0029927Ovarian Cysts1CTD_human
TgeneCDH3C1832162HYPOTRICHOSIS, CONGENITAL, WITH JUVENILE MACULAR DYSTROPHY1CTD_human;ORPHANET;UNIPROT
TgeneCDH3C1857041Ectodermal dysplasia, ectrodactyly, and macular dystrophy1CTD_human;ORPHANET;UNIPROT