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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: 29956

FusionGeneSummary for RAB28_STAP1

check button Fusion gene summary
Fusion gene informationFusion gene name: RAB28_STAP1
Fusion gene ID: 29956
HgeneTgene
Gene symbol

RAB28

STAP1

Gene ID

9364

26228

Gene nameRAB28, member RAS oncogene familysignal transducing adaptor family member 1
SynonymsCORD18BRDG1|STAP-1
Cytomap

4p15.33

4q13.2

Type of geneprotein-codingprotein-coding
Descriptionras-related protein Rab-28signal-transducing adaptor protein 1BCR downstream-signaling protein 1docking protein BRDG1stem cell adaptor protein 1
Modification date2018052620180519
UniProtAcc

P51157

Q9ULZ2

Ensembl transtripts involved in fusion geneENST00000330852, ENST00000288723, 
ENST00000338176, 
ENST00000265404, 
ENST00000396225, 
Fusion gene scores* DoF score3 X 2 X 3=184 X 4 X 3=48
# samples 34
** MAII scorelog2(3/18*10)=0.736965594166206
effective Gene in Pan-Cancer Fusion Genes (eGinPCFGs).
DoF>8 and MAII>0
log2(4/48*10)=-0.263034405833794
possibly effective Gene in Pan-Cancer Fusion Genes (peGinPCFGs).
DoF>8 and MAII<0
Context

PubMed: RAB28 [Title/Abstract] AND STAP1 [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
TgeneSTAP1

GO:0050861

positive regulation of B cell receptor signaling pathway

10518561

TgeneSTAP1

GO:1903997

positive regulation of non-membrane spanning protein tyrosine kinase activity

10518561


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
TCGARVHNSCTCGA-QK-A8Z8-01ARAB28chr4

13462323

-STAP1chr4

68456602

+
* 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-shiftENST00000330852ENST00000265404RAB28chr4

13462323

-STAP1chr4

68456602

+
Frame-shiftENST00000330852ENST00000396225RAB28chr4

13462323

-STAP1chr4

68456602

+
Frame-shiftENST00000288723ENST00000265404RAB28chr4

13462323

-STAP1chr4

68456602

+
Frame-shiftENST00000288723ENST00000396225RAB28chr4

13462323

-STAP1chr4

68456602

+
Frame-shiftENST00000338176ENST00000265404RAB28chr4

13462323

-STAP1chr4

68456602

+
Frame-shiftENST00000338176ENST00000396225RAB28chr4

13462323

-STAP1chr4

68456602

+

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FusionProtFeatures for RAB28_STAP1


check buttonMain function of each fusion partner protein. (from UniProt)
HgeneTgene
RAB28

P51157

STAP1

Q9ULZ2

In BCR signaling, appears to function as a dockingprotein acting downstream of TEC and participates in a positivefeedback loop by increasing the activity of TEC.{ECO:0000269|PubMed:10518561}.

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 RAB28_STAP1


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 RAB28_STAP1


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
RAB28APP, DUSP12, DUSP23, FBXO42, PDE6D, NCOA3, CTSV, CCDC144A, HMMR, KIF7, HSF1, MNS1STAP1SH3KBP1, FAM134C, CD2AP, SULT1A1, CAPZA2, CAPZB, CCND3


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 RAB28_STAP1


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 RAB28_STAP1


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