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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:IGFBP3-SLC2A3 (FusionGDB2 ID:38413)

Fusion Gene Summary for IGFBP3-SLC2A3

check button Fusion gene summary
Fusion gene informationFusion gene name: IGFBP3-SLC2A3
Fusion gene ID: 38413
HgeneTgene
Gene symbol

IGFBP3

SLC2A3

Gene ID

3486

6515

Gene nameinsulin like growth factor binding protein 3solute carrier family 2 member 3
SynonymsBP-53|IBP3GLUT3
Cytomap

7p12.3

12p13.31

Type of geneprotein-codingprotein-coding
Descriptioninsulin-like growth factor-binding protein 3IBP-3IGF-binding protein 3IGFBP-3acid stable subunit of the 140 K IGF complexbinding protein 29binding protein 53growth hormone-dependent binding proteinsolute carrier family 2, facilitated glucose transporter member 3GLUT-3glucose transporter type 3, brainsolute carrier family 2 (facilitated glucose transporter), member 3
Modification date2020031520200320
UniProtAcc

P17936

.
Ensembl transtripts involved in fusion geneENST00000381086, ENST00000275521, 
ENST00000381083, ENST00000465642, 
ENST00000075120, ENST00000543435, 
Fusion gene scores* DoF score9 X 9 X 4=3242 X 2 X 1=4
# samples 92
** MAII scorelog2(9/324*10)=-1.84799690655495
possibly effective Gene in Pan-Cancer Fusion Genes (peGinPCFGs).
DoF>8 and MAII<0
log2(2/4*10)=2.32192809488736
Context

PubMed: IGFBP3 [Title/Abstract] AND SLC2A3 [Title/Abstract] AND fusion [Title/Abstract]

Most frequent breakpointIGFBP3(45960766)-SLC2A3(8083114), # samples:1
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
HgeneIGFBP3

GO:0001933

negative regulation of protein phosphorylation

17591901

HgeneIGFBP3

GO:0006468

protein phosphorylation

17434920

HgeneIGFBP3

GO:0014912

negative regulation of smooth muscle cell migration

10766744

HgeneIGFBP3

GO:0045663

positive regulation of myoblast differentiation

12599210

HgeneIGFBP3

GO:0048662

negative regulation of smooth muscle cell proliferation

10766744

TgeneSLC2A3

GO:1904659

glucose transmembrane transport

26176916


check buttonFusion gene breakpoints across IGFBP3 (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 SLC2A3 (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/ADA576628IGFBP3chr7

45960766

-SLC2A3chr12

8083114

-


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Fusion Gene ORF analysis for IGFBP3-SLC2A3

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-3CDSENST00000381086ENST00000075120IGFBP3chr7

45960766

-SLC2A3chr12

8083114

-
intron-intronENST00000381086ENST00000543435IGFBP3chr7

45960766

-SLC2A3chr12

8083114

-
intron-3CDSENST00000275521ENST00000075120IGFBP3chr7

45960766

-SLC2A3chr12

8083114

-
intron-intronENST00000275521ENST00000543435IGFBP3chr7

45960766

-SLC2A3chr12

8083114

-
intron-3CDSENST00000381083ENST00000075120IGFBP3chr7

45960766

-SLC2A3chr12

8083114

-
intron-intronENST00000381083ENST00000543435IGFBP3chr7

45960766

-SLC2A3chr12

8083114

-
intron-3CDSENST00000465642ENST00000075120IGFBP3chr7

45960766

-SLC2A3chr12

8083114

-
intron-intronENST00000465642ENST00000543435IGFBP3chr7

45960766

-SLC2A3chr12

8083114

-

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 IGFBP3-SLC2A3


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 IGFBP3-SLC2A3


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
IGFBP3

P17936

.
FUNCTION: IGF-binding proteins prolong the half-life of the IGFs and have been shown to either inhibit or stimulate the growth promoting effects of the IGFs on cell culture. They alter the interaction of IGFs with their cell surface receptors. Also exhibits IGF-independent antiproliferative and apoptotic effects mediated by its receptor TMEM219/IGFBP-3R. {ECO:0000269|PubMed:20353938}.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.

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 IGFBP3-SLC2A3


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 IGFBP3-SLC2A3


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 IGFBP3-SLC2A3


check button Drugs targeting genes involved in this fusion gene.
(DrugBank Version 5.1.8 2021-05-08)
PartnerGeneUniProtAccDrugBank IDDrug nameDrug activityDrug typeDrug status
HgeneIGFBP3P17936DB00523AlitretinoinSmall moleculeApproved|Investigational
HgeneIGFBP3P17936DB00523AlitretinoinSmall moleculeApproved|Investigational
HgeneIGFBP3P17936DB01277MecaserminBiotechApproved|Investigational
HgeneIGFBP3P17936DB01277MecaserminBiotechApproved|Investigational

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Related Diseases for IGFBP3-SLC2A3


check button Diseases associated with fusion partners.
(DisGeNet 4.0)
PartnerGeneDisease IDDisease name# pubmedsSource
HgeneIGFBP3C0033578Prostatic Neoplasms3CTD_human
HgeneIGFBP3C0376358Malignant neoplasm of prostate3CTD_human
HgeneIGFBP3C0000786Spontaneous abortion1CTD_human
HgeneIGFBP3C0000822Abortion, Tubal1CTD_human
HgeneIGFBP3C0003873Rheumatoid Arthritis1CTD_human
HgeneIGFBP3C0004352Autistic Disorder1CTD_human
HgeneIGFBP3C0005684Malignant neoplasm of urinary bladder1CTD_human
HgeneIGFBP3C0005695Bladder Neoplasm1CTD_human
HgeneIGFBP3C0007138Carcinoma, Transitional Cell1CTD_human
HgeneIGFBP3C0009402Colorectal Carcinoma1CTD_human;UNIPROT
HgeneIGFBP3C0009404Colorectal Neoplasms1CTD_human
HgeneIGFBP3C0023893Liver Cirrhosis, Experimental1CTD_human
HgeneIGFBP3C0024623Malignant neoplasm of stomach1CTD_human
HgeneIGFBP3C0038356Stomach Neoplasms1CTD_human
HgeneIGFBP3C0151744Myocardial Ischemia1CTD_human
HgeneIGFBP3C0175693Russell-Silver syndrome1GENOMICS_ENGLAND
HgeneIGFBP3C1708349Hereditary Diffuse Gastric Cancer1CTD_human
HgeneIGFBP3C3830362Early Pregnancy Loss1CTD_human
HgeneIGFBP3C4552766Miscarriage1CTD_human
TgeneSLC2A3C0023794Lipoidosis2CTD_human
TgeneSLC2A3C0020179Huntington Disease1ORPHANET
TgeneSLC2A3C0027654Embryonal Neoplasm1CTD_human
TgeneSLC2A3C0027658Neoplasms, Germ Cell and Embryonal1CTD_human
TgeneSLC2A3C0087031Juvenile-Onset Still Disease1CTD_human
TgeneSLC2A3C0162820Dermatitis, Allergic Contact1CTD_human
TgeneSLC2A3C0205851Germ cell tumor1CTD_human
TgeneSLC2A3C0205852Neoplasms, Embryonal and Mixed1CTD_human
TgeneSLC2A3C0740345Germ Cell Cancer1CTD_human
TgeneSLC2A3C0751364Cancer, Embryonal1CTD_human
TgeneSLC2A3C0751365Cancer, Embryonal and Mixed1CTD_human
TgeneSLC2A3C3495559Juvenile arthritis1CTD_human
TgeneSLC2A3C3714758Juvenile psoriatic arthritis1CTD_human
TgeneSLC2A3C4552091Polyarthritis, Juvenile, Rheumatoid Factor Negative1CTD_human
TgeneSLC2A3C4704862Polyarthritis, Juvenile, Rheumatoid Factor Positive1CTD_human