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Center for Computational Systems Medicine
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Fusion Gene Summary

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Fusion Gene ORF analysis

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Fusion Genomic Features

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Fusion Protein Features

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Fusion Gene Sequence

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Fusion Gene PPI analysis

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Related Drugs

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Related Diseases

Fusion gene:SLU7-BCR (FusionGDB2 ID:83143)

Fusion Gene Summary for SLU7-BCR

check button Fusion gene summary
Fusion gene informationFusion gene name: SLU7-BCR
Fusion gene ID: 83143
HgeneTgene
Gene symbol

SLU7

BCR

Gene ID

10569

613

Gene nameSLU7 homolog, splicing factorBCR activator of RhoGEF and GTPase
Synonyms9G8|hSlu7ALL|BCR1|CML|D22S11|D22S662|PHL
Cytomap

5q33.3

22q11.23

Type of geneprotein-codingprotein-coding
Descriptionpre-mRNA-splicing factor SLU7SLU7 splicing factor homologsplicing factorstep II splicing factor SLU7zinc knuckle motif containingbreakpoint cluster region proteinBCR, RhoGEF and GTPase activating proteinBCR/FGFR1 chimera proteinFGFR1/BCR chimera proteinbreakpoint cluster regionrenal carcinoma antigen NY-REN-26
Modification date2020031320200313
UniProtAcc.

P11274

Ensembl transtripts involved in fusion geneENST00000297151, ENST00000305877, 
ENST00000359540, ENST00000398512, 
ENST00000436990, 
Fusion gene scores* DoF score5 X 5 X 2=5015 X 58 X 7=6090
# samples 561
** MAII scorelog2(5/50*10)=0log2(61/6090*10)=-3.31956108034345
possibly effective Gene in Pan-Cancer Fusion Genes (peGinPCFGs).
DoF>8 and MAII<0
Context

PubMed: SLU7 [Title/Abstract] AND BCR [Title/Abstract] AND fusion [Title/Abstract]

Most frequent breakpointSLU7(159835674)-BCR(23629344), # samples:2
Anticipated loss of major functional domain due to fusion event.
* 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
HgeneSLU7

GO:0000375

RNA splicing, via transesterification reactions

10197984

HgeneSLU7

GO:0000380

alternative mRNA splicing, via spliceosome

15728250

HgeneSLU7

GO:0000389

mRNA 3'-splice site recognition

15728250

HgeneSLU7

GO:0006886

intracellular protein transport

21122810

HgeneSLU7

GO:0034605

cellular response to heat

21122810

TgeneBCR

GO:0090630

activation of GTPase activity

7479768


check buttonFusion gene breakpoints across SLU7 (5'-gene)
* Click on the image to open the UCSC genome browser with custom track showing this image in a new window.

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

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
ChiTaRS5.0N/ABF094682SLU7chr5

159835674

-BCRchr22

23629344

+
ChiTaRS5.0N/ABF380221SLU7chr5

159835674

-BCRchr22

23629344

+


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Fusion Gene ORF analysis for SLU7-BCR

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
intron-3CDSENST00000297151ENST00000305877SLU7chr5

159835674

-BCRchr22

23629344

+
intron-3CDSENST00000297151ENST00000359540SLU7chr5

159835674

-BCRchr22

23629344

+
intron-intronENST00000297151ENST00000398512SLU7chr5

159835674

-BCRchr22

23629344

+
intron-intronENST00000297151ENST00000436990SLU7chr5

159835674

-BCRchr22

23629344

+

check buttonORFfinder result based on the fusion transcript sequence of in-frame fusion genes.
HenstTenstHgeneHchrHbpHstrandTgeneTchrTbpTstrandSeq length
(transcript)
BP loci
(transcript)
Predicted start
(transcript)
Predicted stop
(transcript)
Seq length
(amino acids)

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

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Fusion Genomic Features for SLU7-BCR


check buttonFusionAI prediction of the potential fusion gene breakpoint based on the pre-mature RNA sequence context (+/- 5kb of individual partner genes, total 20kb length sequence). FusionAI is a fusion gene breakpoint classifier based on convolutional neural network by comparing the fusion positive and negative sequence context of ~ 20K fusion gene data. From here, we can have the relative potentency of the 20K genomic sequence how individual sequnce will be likely used as the gene fusion breakpoints.
HgeneHchrHbpHstrandTgeneTchrTbpTstrand1-pp (fusion gene breakpoint)

check buttonDistribution of 44 human genomic features loci across 20kb length fusion breakpoint regions. We integrated a total of 44 different types of human genomic feature loci information across five big categories including virus integration sites, repeats, structural variants, chromatin states, and gene expression regulation. More details are in help page.

check buttonDistribution of 44 human genomic features loci across 20kb length fusion breakpoint regions that are ovelapped with the top 1% feature importance score regions. More details are in help page.

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Fusion Protein Features for SLU7-BCR


check button Go to

FGviewer for the breakpoints of :-:

.
- FGviewer provides the online visualization of the retention search of the protein functional features across DNA, RNA, protein, and pathological levels.
FGviewer

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

P11274

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: Protein with a unique structure having two opposing regulatory activities toward small GTP-binding proteins. The C-terminus is a GTPase-activating protein (GAP) domain which stimulates GTP hydrolysis by RAC1, RAC2 and CDC42. Accelerates the intrinsic rate of GTP hydrolysis of RAC1 or CDC42, leading to down-regulation of the active GTP-bound form (PubMed:7479768, PubMed:1903516, PubMed:17116687). The central Dbl homology (DH) domain functions as guanine nucleotide exchange factor (GEF) that modulates the GTPases CDC42, RHOA and RAC1. Promotes the conversion of CDC42, RHOA and RAC1 from the GDP-bound to the GTP-bound form (PubMed:7479768, PubMed:23940119). The amino terminus contains an intrinsic kinase activity (PubMed:1657398). Functions as an important negative regulator of neuronal RAC1 activity (By similarity). Regulates macrophage functions such as CSF1-directed motility and phagocytosis through the modulation of RAC1 activity (PubMed:17116687). Plays a major role as a RHOA GEF in keratinocytes being involved in focal adhesion formation and keratinocyte differentiation (PubMed:23940119). {ECO:0000250|UniProtKB:Q6PAJ1, ECO:0000269|PubMed:1657398, ECO:0000269|PubMed:17116687, ECO:0000269|PubMed:1903516, ECO:0000269|PubMed:23940119, ECO:0000269|PubMed:7479768}.

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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Fusion Gene Sequence for SLU7-BCR


check button For in-frame fusion transcripts, we provide the fusion transcript sequences and fusion amino acid sequences. To have fusion amino acid sequence, we ran ORFfinder and chose the longest ORF among the all predicted ones.

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Fusion Gene PPI Analysis for SLU7-BCR


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


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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Related Drugs for SLU7-BCR


check button Drugs targeting genes involved in this fusion gene.
(DrugBank Version 5.1.8 2021-05-08)
PartnerGeneUniProtAccDrugBank IDDrug nameDrug activityDrug typeDrug status
TgeneBCRP11274DB00619ImatinibInhibitorSmall moleculeApproved
TgeneBCRP11274DB00619ImatinibInhibitorSmall moleculeApproved
TgeneBCRP11274DB00619ImatinibInhibitorSmall moleculeApproved
TgeneBCRP11274DB06616BosutinibInhibitorSmall moleculeApproved
TgeneBCRP11274DB06616BosutinibInhibitorSmall moleculeApproved
TgeneBCRP11274DB06616BosutinibInhibitorSmall moleculeApproved
TgeneBCRP11274DB01254DasatinibSmall moleculeApproved|Investigational
TgeneBCRP11274DB01254DasatinibSmall moleculeApproved|Investigational
TgeneBCRP11274DB01254DasatinibSmall moleculeApproved|Investigational
TgeneBCRP11274DB08901PonatinibInhibitorSmall moleculeApproved|Investigational
TgeneBCRP11274DB08901PonatinibInhibitorSmall moleculeApproved|Investigational
TgeneBCRP11274DB08901PonatinibInhibitorSmall moleculeApproved|Investigational

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Related Diseases for SLU7-BCR


check button Diseases associated with fusion partners.
(DisGeNet 4.0)
PartnerGeneDisease IDDisease name# pubmedsSource
HgeneSLU7C0043094Weight Gain1CTD_human
TgeneBCRC0005586Bipolar Disorder4PSYGENET
TgeneBCRC0023473Myeloid Leukemia, Chronic3CTD_human;ORPHANET
TgeneBCRC0005699Blast Phase1CTD_human
TgeneBCRC0006413Burkitt Lymphoma1ORPHANET
TgeneBCRC0023893Liver Cirrhosis, Experimental1CTD_human
TgeneBCRC0027022Myeloproliferative disease1CTD_human
TgeneBCRC0027540Necrosis1CTD_human
TgeneBCRC0027659Neoplasms, Experimental1CTD_human
TgeneBCRC0041696Unipolar Depression1PSYGENET
TgeneBCRC1269683Major Depressive Disorder1PSYGENET
TgeneBCRC1292769Precursor B-cell lymphoblastic leukemia1ORPHANET