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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:IGF2R-PREP (FusionGDB2 ID:38385)

Fusion Gene Summary for IGF2R-PREP

check button Fusion gene summary
Fusion gene informationFusion gene name: IGF2R-PREP
Fusion gene ID: 38385
HgeneTgene
Gene symbol

IGF2R

PREP

Gene ID

3482

5550

Gene nameinsulin like growth factor 2 receptorprolyl endopeptidase
SynonymsCD222|CI-M6PR|CIMPR|M6P-R|M6P/IGF2R|MPR 300|MPR1|MPR300|MPRIPE|PEP
Cytomap

6q25.3

6q21

Type of geneprotein-codingprotein-coding
Descriptioncation-independent mannose-6-phosphate receptor300 kDa mannose 6-phosphate receptorCI Man-6-P receptorIGF-II receptorM6P/IGF2 receptorinsulin-like growth factor II receptorprolyl endopeptidasedJ355L5.1 (prolyl endopeptidase)post-proline cleaving enzymeprolyl oligopeptidase
Modification date2020031520200313
UniProtAcc

P11717

PNOC

Ensembl transtripts involved in fusion geneENST00000356956, ENST00000475584, 
ENST00000369110, 
Fusion gene scores* DoF score23 X 16 X 11=40488 X 4 X 8=256
# samples 259
** MAII scorelog2(25/4048*10)=-4.01720929003222
possibly effective Gene in Pan-Cancer Fusion Genes (peGinPCFGs).
DoF>8 and MAII<0
log2(9/256*10)=-1.50814690367033
possibly effective Gene in Pan-Cancer Fusion Genes (peGinPCFGs).
DoF>8 and MAII<0
Context

PubMed: IGF2R [Title/Abstract] AND PREP [Title/Abstract] AND fusion [Title/Abstract]

Most frequent breakpointIGF2R(160461756)-PREP(105845802), # samples:1
Anticipated loss of major functional domain due to fusion event.IGF2R-PREP seems lost the major protein functional domain in Hgene partner, which is a tumor suppressor due to the frame-shifted ORF.
IGF2R-PREP seems lost the major protein functional domain in Tgene partner, which is a essential gene due to the frame-shifted ORF.
IGF2R-PREP 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

check buttonFusion gene breakpoints across IGF2R (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 PREP (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
ChimerDB4BRCATCGA-E9-A248-01AIGF2Rchr6

160461756

-PREPchr6

105845802

-


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Fusion Gene ORF analysis for IGF2R-PREP

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-shiftENST00000356956ENST00000369110IGF2Rchr6

160461756

-PREPchr6

105845802

-
intron-3CDSENST00000475584ENST00000369110IGF2Rchr6

160461756

-PREPchr6

105845802

-

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 IGF2R-PREP


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 IGF2R-PREP


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
IGF2R

P11717

PREP

PNOC

FUNCTION: Mediates the transport of phosphorylated lysosomal enzymes from the Golgi complex and the cell surface to lysosomes (PubMed:2963003, PubMed:18817523). Lysosomal enzymes bearing phosphomannosyl residues bind specifically to mannose-6-phosphate receptors in the Golgi apparatus and the resulting receptor-ligand complex is transported to an acidic prelysosomal compartment where the low pH mediates the dissociation of the complex (PubMed:2963003, PubMed:18817523). The receptor is then recycled back to the Golgi for another round of trafficking through its binding to the retromer (PubMed:18817523). This receptor also binds IGF2 (PubMed:18046459). Acts as a positive regulator of T-cell coactivation by binding DPP4 (PubMed:10900005). {ECO:0000269|PubMed:10900005, ECO:0000269|PubMed:18046459, ECO:0000269|PubMed:18817523, ECO:0000269|PubMed:2963003}.176

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 IGF2R-PREP


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 IGF2R-PREP


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 IGF2R-PREP


check button Drugs targeting genes involved in this fusion gene.
(DrugBank Version 5.1.8 2021-05-08)
PartnerGeneUniProtAccDrugBank IDDrug nameDrug activityDrug typeDrug status
HgeneIGF2RP11717DB14751Mecasermin rinfabateBiotechApproved
HgeneIGF2RP11717DB14751Mecasermin rinfabateBiotechApproved
HgeneIGF2RP11717DB01277MecaserminBiotechApproved|Investigational
HgeneIGF2RP11717DB01277MecaserminBiotechApproved|Investigational
HgeneIGF2RP11717DB13173Cerliponase alfaLigandBiotechApproved|Investigational
HgeneIGF2RP11717DB13173Cerliponase alfaLigandBiotechApproved|Investigational

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Related Diseases for IGF2R-PREP


check button Diseases associated with fusion partners.
(DisGeNet 4.0)
PartnerGeneDisease IDDisease name# pubmedsSource
HgeneIGF2RC0024115Lung diseases2CTD_human
HgeneIGF2RC0235833Congenital diaphragmatic hernia2CTD_human
HgeneIGF2RC0265699Congenital hernia of foramen of Morgagni2CTD_human
HgeneIGF2RC0265700Congenital hernia of foramen of Bochdalek2CTD_human
HgeneIGF2RC0002395Alzheimer's Disease1CTD_human
HgeneIGF2RC0011265Presenile dementia1CTD_human
HgeneIGF2RC0023893Liver Cirrhosis, Experimental1CTD_human
HgeneIGF2RC0030567Parkinson Disease1CTD_human
HgeneIGF2RC0033578Prostatic Neoplasms1CTD_human
HgeneIGF2RC0242973Ventricular Dysfunction1CTD_human
HgeneIGF2RC0276496Familial Alzheimer Disease (FAD)1CTD_human
HgeneIGF2RC0376358Malignant neoplasm of prostate1CTD_human
HgeneIGF2RC0494463Alzheimer Disease, Late Onset1CTD_human
HgeneIGF2RC0546126Acute Confusional Senile Dementia1CTD_human
HgeneIGF2RC0553980Endomyocardial Fibrosis1CTD_human
HgeneIGF2RC0750900Alzheimer's Disease, Focal Onset1CTD_human
HgeneIGF2RC0750901Alzheimer Disease, Early Onset1CTD_human
HgeneIGF2RC0752347Lewy Body Disease1CTD_human
HgeneIGF2RC2239176Liver carcinoma1CGI;CTD_human
TgenePREPC0002622Amnesia1CTD_human
TgenePREPC0002624Retrograde amnesia1CTD_human
TgenePREPC0024623Malignant neoplasm of stomach1CTD_human
TgenePREPC0038356Stomach Neoplasms1CTD_human
TgenePREPC0233750Hysterical amnesia1CTD_human
TgenePREPC0233796Temporary Amnesia1CTD_human
TgenePREPC0235874Disease Exacerbation1CTD_human
TgenePREPC0236795Dissociative Amnesia1CTD_human
TgenePREPC0262497Global Amnesia1CTD_human
TgenePREPC0338831Manic1PSYGENET
TgenePREPC0750906Tactile Amnesia1CTD_human
TgenePREPC0750907Amnestic State1CTD_human
TgenePREPC0750908Pre-Ictal Amnesia1CTD_human
TgenePREPC0750909Retrograde Memory Loss1CTD_human
TgenePREPC0750910Pre-Ictal Memory Loss1CTD_human
TgenePREPC1708349Hereditary Diffuse Gastric Cancer1CTD_human