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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:CABIN1-SLC2A11 (FusionGDB2 ID:HG23523TG66035)

Fusion Gene Summary for CABIN1-SLC2A11

check button Fusion gene summary
Fusion gene informationFusion gene name: CABIN1-SLC2A11
Fusion gene ID: hg23523tg66035
HgeneTgene
Gene symbol

CABIN1

SLC2A11

Gene ID

23523

66035

Gene namecalcineurin binding protein 1solute carrier family 2 member 11
SynonymsCAIN|KB-318B8.7|PPP3INGLUT10|GLUT11
Cytomap('CABIN1')('SLC2A11')

22q11.23

22q11.23

Type of geneprotein-codingprotein-coding
Descriptioncalcineurin-binding protein cabin-1calcineurin binding protein cabin 1calcineurin inhibitorsolute carrier family 2, facilitated glucose transporter member 11facilitative glucose transporter GLUT11glucose transporter protein 10glucose transporter protein 11glucose transporter type 10glucose transporter type 11glucose transporter-like prote
Modification date2020031320200313
UniProtAcc

Q9Y6J0

.
Ensembl transtripts involved in fusion geneENST00000263119, ENST00000398319, 
ENST00000405822, ENST00000337989, 
ENST00000485008, 
Fusion gene scores* DoF score16 X 15 X 8=19202 X 2 X 2=8
# samples 182
** MAII scorelog2(18/1920*10)=-3.41503749927884
possibly effective Gene in Pan-Cancer Fusion Genes (peGinPCFGs).
DoF>8 and MAII<0
log2(2/8*10)=1.32192809488736
Context

PubMed: CABIN1 [Title/Abstract] AND SLC2A11 [Title/Abstract] AND fusion [Title/Abstract]

Most frequent breakpointCABIN1(24515665)-SLC2A11(24224646), # samples:2
Anticipated loss of major functional domain due to fusion event.CABIN1-SLC2A11 seems lost the major protein functional domain in Hgene partner, which is a essential gene due to the frame-shifted ORF.
CABIN1-SLC2A11 seems lost the major protein functional domain in Tgene partner, which is a IUPHAR drug target due to the frame-shifted ORF.
* 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
HgeneCABIN1

GO:0006336

DNA replication-independent nucleosome assembly

14718166

TgeneSLC2A11

GO:1904659

glucose transmembrane transport

12175779



check button Fusion gene information
* 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
ChimerDB4UCSTCGA-N8-A4PL-01ACABIN1chr22

24515665

+SLC2A11chr22

24224646

+
ChimerDB4UCSTCGA-N8-A4PLCABIN1chr22

24515665

+SLC2A11chr22

24224646

+


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Fusion Gene ORF analysis for CABIN1-SLC2A11

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-3UTRENST00000263119ENST00000316185CABIN1chr22

24515665

+SLC2A11chr22

24224646

+
5CDS-3UTRENST00000263119ENST00000467660CABIN1chr22

24515665

+SLC2A11chr22

24224646

+
5CDS-3UTRENST00000398319ENST00000316185CABIN1chr22

24515665

+SLC2A11chr22

24224646

+
5CDS-3UTRENST00000398319ENST00000467660CABIN1chr22

24515665

+SLC2A11chr22

24224646

+
5CDS-3UTRENST00000405822ENST00000316185CABIN1chr22

24515665

+SLC2A11chr22

24224646

+
5CDS-3UTRENST00000405822ENST00000467660CABIN1chr22

24515665

+SLC2A11chr22

24224646

+
5CDS-intronENST00000263119ENST00000398356CABIN1chr22

24515665

+SLC2A11chr22

24224646

+
5CDS-intronENST00000263119ENST00000403208CABIN1chr22

24515665

+SLC2A11chr22

24224646

+
5CDS-intronENST00000263119ENST00000405847CABIN1chr22

24515665

+SLC2A11chr22

24224646

+
5CDS-intronENST00000398319ENST00000398356CABIN1chr22

24515665

+SLC2A11chr22

24224646

+
5CDS-intronENST00000398319ENST00000403208CABIN1chr22

24515665

+SLC2A11chr22

24224646

+
5CDS-intronENST00000398319ENST00000405847CABIN1chr22

24515665

+SLC2A11chr22

24224646

+
5CDS-intronENST00000405822ENST00000398356CABIN1chr22

24515665

+SLC2A11chr22

24224646

+
5CDS-intronENST00000405822ENST00000403208CABIN1chr22

24515665

+SLC2A11chr22

24224646

+
5CDS-intronENST00000405822ENST00000405847CABIN1chr22

24515665

+SLC2A11chr22

24224646

+
Frame-shiftENST00000263119ENST00000345044CABIN1chr22

24515665

+SLC2A11chr22

24224646

+
Frame-shiftENST00000398319ENST00000345044CABIN1chr22

24515665

+SLC2A11chr22

24224646

+
Frame-shiftENST00000405822ENST00000345044CABIN1chr22

24515665

+SLC2A11chr22

24224646

+
intron-3CDSENST00000337989ENST00000345044CABIN1chr22

24515665

+SLC2A11chr22

24224646

+
intron-3CDSENST00000485008ENST00000345044CABIN1chr22

24515665

+SLC2A11chr22

24224646

+
intron-3UTRENST00000337989ENST00000316185CABIN1chr22

24515665

+SLC2A11chr22

24224646

+
intron-3UTRENST00000337989ENST00000467660CABIN1chr22

24515665

+SLC2A11chr22

24224646

+
intron-3UTRENST00000485008ENST00000316185CABIN1chr22

24515665

+SLC2A11chr22

24224646

+
intron-3UTRENST00000485008ENST00000467660CABIN1chr22

24515665

+SLC2A11chr22

24224646

+
intron-intronENST00000337989ENST00000398356CABIN1chr22

24515665

+SLC2A11chr22

24224646

+
intron-intronENST00000337989ENST00000403208CABIN1chr22

24515665

+SLC2A11chr22

24224646

+
intron-intronENST00000337989ENST00000405847CABIN1chr22

24515665

+SLC2A11chr22

24224646

+
intron-intronENST00000485008ENST00000398356CABIN1chr22

24515665

+SLC2A11chr22

24224646

+
intron-intronENST00000485008ENST00000403208CABIN1chr22

24515665

+SLC2A11chr22

24224646

+
intron-intronENST00000485008ENST00000405847CABIN1chr22

24515665

+SLC2A11chr22

24224646

+

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 CABIN1-SLC2A11


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)
CABIN1chr2224515665+SLC2A11chr2224224645+1.84E-070.99999976
CABIN1chr2224515665+SLC2A11chr2224224645+1.84E-070.99999976
CABIN1chr2224515665+SLC2A11chr2224224645+1.84E-070.99999976
CABIN1chr2224515665+SLC2A11chr2224224645+1.84E-070.99999976


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.
genomic feature of top 1%

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Fusion Protein Features for CABIN1-SLC2A11


check button Four levels of functional features of fusion genes
Go to FGviewer search page for the most frequent breakpoint (https://ccsmweb.uth.edu/FGviewer/:24515665/:24224646)
- FGviewer provides the online visualization of the retention search of the protein functional features across DNA, RNA, protein, and pathological levels.
- How to search
1. Put your fusion gene symbol.
2. Press the tab key until there will be shown the breakpoint information filled.
4. Go down and press 'Search' tab twice.
4. Go down to have the hyperlink of the search result.
5. Click the hyperlink.
6. See the FGviewer result for your fusion gene.
FGviewer

check buttonMain function of each fusion partner protein. (from UniProt)
HgeneTgene
CABIN1

Q9Y6J0

.
FUNCTION: May be required for replication-independent chromatin assembly. May serve as a negative regulator of T-cell receptor (TCR) signaling via inhibition of calcineurin. Inhibition of activated calcineurin is dependent on both PKC and calcium signals. Acts as a negative regulator of p53/TP53 by keeping p53 in an inactive state on chromatin at promoters of a subset of it's target genes. {ECO:0000269|PubMed:14718166, ECO:0000269|PubMed:9655484}.FUNCTION: Transcriptional activator which is required for calcium-dependent dendritic growth and branching in cortical neurons. Recruits CREB-binding protein (CREBBP) to nuclear bodies. Component of the CREST-BRG1 complex, a multiprotein complex that regulates promoter activation by orchestrating a calcium-dependent release of a repressor complex and a recruitment of an activator complex. In resting neurons, transcription of the c-FOS promoter is inhibited by BRG1-dependent recruitment of a phospho-RB1-HDAC1 repressor complex. Upon calcium influx, RB1 is dephosphorylated by calcineurin, which leads to release of the repressor complex. At the same time, there is increased recruitment of CREBBP to the promoter by a CREST-dependent mechanism, which leads to transcriptional activation. The CREST-BRG1 complex also binds to the NR2B promoter, and activity-dependent induction of NR2B expression involves a release of HDAC1 and recruitment of CREBBP (By similarity). {ECO:0000250}.

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 CABIN1-SLC2A11


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 CABIN1-SLC2A11


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 CABIN1-SLC2A11


check button Drugs targeting genes involved in this fusion gene.
(DrugBank Version 5.1.8 2021-05-08)
PartnerGeneUniProtAccDrugBank IDDrug nameDrug activityDrug typeDrug status

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Related Diseases for CABIN1-SLC2A11


check button Diseases associated with fusion partners.
(DisGeNet 4.0)
PartnerGeneDisease IDDisease name# pubmedsSource
HgeneCABIN1C0018800Cardiomegaly1CTD_human
HgeneCABIN1C1383860Cardiac Hypertrophy1CTD_human