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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: 2249

FusionGeneSummary for APPBP2_WISP2

check button Fusion gene summary
Fusion gene informationFusion gene name: APPBP2_WISP2
Fusion gene ID: 2249
HgeneTgene
Gene symbol

APPBP2

WISP2

Gene ID

10513

8839

Gene nameamyloid beta precursor protein binding protein 2WNT1 inducible signaling pathway protein 2
SynonymsAPP-BP2|HS.84084|PAT1CCN5|CT58|CTGF-L
Cytomap

17q23.2

20q13.12

Type of geneprotein-codingprotein-coding
Descriptionamyloid protein-binding protein 2amyloid beta precursor protein (cytoplasmic tail) binding protein 2protein interacting with APP tail 1WNT1-inducible-signaling pathway protein 2CCN family member 5connective tissue growth factor-like proteinconnective tissue growth factor-related protein 58
Modification date2018051920180523
UniProtAcc

Q92624

O76076

Ensembl transtripts involved in fusion geneENST00000083182, ENST00000592995, 
ENST00000372868, ENST00000372865, 
ENST00000190983, ENST00000471629, 
Fusion gene scores* DoF score8 X 5 X 4=1602 X 2 X 2=8
# samples 82
** MAII scorelog2(8/160*10)=-1
possibly effective Gene in Pan-Cancer Fusion Genes (peGinPCFGs).
DoF>8 and MAII<0
log2(2/8*10)=1.32192809488736
Context

PubMed: APPBP2 [Title/Abstract] AND WISP2 [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
HgeneAPPBP2

GO:0046907

intracellular transport

9843960


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-AC-A62V-01AAPPBP2chr17

58556509

-WISP2chr20

43348538

+
* 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-shiftENST00000083182ENST00000372868APPBP2chr17

58556509

-WISP2chr20

43348538

+
Frame-shiftENST00000083182ENST00000372865APPBP2chr17

58556509

-WISP2chr20

43348538

+
Frame-shiftENST00000083182ENST00000190983APPBP2chr17

58556509

-WISP2chr20

43348538

+
5CDS-intronENST00000083182ENST00000471629APPBP2chr17

58556509

-WISP2chr20

43348538

+
intron-3CDSENST00000592995ENST00000372868APPBP2chr17

58556509

-WISP2chr20

43348538

+
intron-3CDSENST00000592995ENST00000372865APPBP2chr17

58556509

-WISP2chr20

43348538

+
intron-3CDSENST00000592995ENST00000190983APPBP2chr17

58556509

-WISP2chr20

43348538

+
intron-intronENST00000592995ENST00000471629APPBP2chr17

58556509

-WISP2chr20

43348538

+

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FusionProtFeatures for APPBP2_WISP2


check buttonMain function of each fusion partner protein. (from UniProt)
HgeneTgene
APPBP2

Q92624

WISP2

O76076

May play a role in intracellular protein transport. Maybe involved in the translocation of APP along microtubules towardthe cell surface. {ECO:0000269|PubMed:9843960}. May play an important role in modulating bone turnover.Promotes the adhesion of osteoblast cells and inhibits the bindingof fibrinogen to integrin receptors. In addition, inhibitsosteocalcin production.

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 APPBP2_WISP2


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 APPBP2_WISP2


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
APPBP2APP, CNTFR, MUL1, EID3, MFSD3, CREB3, WDR24, ZCCHC12, WNT5B, RRS1, SLC22A6, MLLT3, TBL3, KIF6, PCSK5, CHMP5, SYT11, NFYA, SCFD1, UBC, TCEB2, TCEB1, CUL2, COPS6, FAM92A1, RASSF5, GP9, FSTL1, AHCY, CALM3, CLCN1, CSNK1G2, DPEP1, GALNT3, GSTP1, HSPA4, CDK16, PPP1R8, PRKAA2, PRKACB, TAF11, WAS, NPRL3, HIST1H2AK, KLF11, AIM2, DHRS2, CORO2B, SYNRG, TCF25, SNX5, ST8SIA5, ERO1L, AK3, LUZP4, LUC7L2, FXYD7, UBE2R2, ANKRD10, UGGT2, LANCL2, CCNL1, ARMCX5, ZNF747, C1orf50, SLC25A23, RNF128, LONRF3, CTC1, RNF34, PYROXD2, ZC3H10, EPT1, DCD, HIPK4, FAM19A4, COL24A1, GCSAM, KLHL35, CCDC85C, SELV, PI4KAP2, MGC34796, C6orf226, IKBKE, C1QTNF2, XRCC4, SKAP1, COPS2, COPS3, AP4S1, RASSF8, SLAIN2, KBTBD7, COPS8, GLMN, COPS7B, DOCK8, INTU, ZNF232, MYCL, IKZF1, THOC3, NPRL2, FBXL5, GNA15, ZNF785, DQX1, ZIM2, GATAD2A, USP25, THSD4, ZNF408, FAM107AWISP2HDAC1, HDAC3, PRKRIR, CTU2, AMZ2, TRIM68, PITHD1, ICAM1


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 APPBP2_WISP2


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 APPBP2_WISP2


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