FusionGDB Logo

Home

Download

Statistics

Examples

Help

Contact

Center for Computational Systems Medicine
leaf

Fusion Gene Summary

leaf

Fusion Gene ORF analysis

leaf

Fusion Genomic Features

leaf

Fusion Protein Features

leaf

Fusion Gene Sequence

leaf

Fusion Gene PPI analysis

leaf

Related Drugs

leaf

Related Diseases

Fusion gene:IGF2R-ACVR2A (FusionGDB2 ID:38371)

Fusion Gene Summary for IGF2R-ACVR2A

check button Fusion gene summary
Fusion gene informationFusion gene name: IGF2R-ACVR2A
Fusion gene ID: 38371
HgeneTgene
Gene symbol

IGF2R

ACVR2A

Gene ID

3482

92

Gene nameinsulin like growth factor 2 receptoractivin A receptor type 2A
SynonymsCD222|CI-M6PR|CIMPR|M6P-R|M6P/IGF2R|MPR 300|MPR1|MPR300|MPRIACTRII|ACVR2
Cytomap

6q25.3

2q22.3-q23.1

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 receptoractivin receptor type-2Aactivin A receptor, type IIA
Modification date2020031520200313
UniProtAcc

P11717

P27037

Ensembl transtripts involved in fusion geneENST00000356956, ENST00000475584, 
ENST00000535787, ENST00000241416, 
ENST00000404590, ENST00000495775, 
Fusion gene scores* DoF score23 X 16 X 11=40485 X 6 X 5=150
# samples 256
** MAII scorelog2(25/4048*10)=-4.01720929003222
possibly effective Gene in Pan-Cancer Fusion Genes (peGinPCFGs).
DoF>8 and MAII<0
log2(6/150*10)=-1.32192809488736
possibly effective Gene in Pan-Cancer Fusion Genes (peGinPCFGs).
DoF>8 and MAII<0
Context

PubMed: IGF2R [Title/Abstract] AND ACVR2A [Title/Abstract] AND fusion [Title/Abstract]

Most frequent breakpointIGF2R(160390427)-ACVR2A(148672760), # samples:3
Anticipated loss of major functional domain due to fusion event.IGF2R-ACVR2A seems lost the major protein functional domain in Hgene partner, which is a tumor suppressor due to the frame-shifted ORF.
IGF2R-ACVR2A seems lost the major protein functional domain in Tgene partner, which is a kinase due to the frame-shifted ORF.
IGF2R-ACVR2A seems lost the major protein functional domain in Tgene partner, which is a CGC due to the frame-shifted ORF.
IGF2R-ACVR2A 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
TgeneACVR2A

GO:0030509

BMP signaling pathway

18436533

TgeneACVR2A

GO:0032927

positive regulation of activin receptor signaling pathway

12665502

TgeneACVR2A

GO:0045648

positive regulation of erythrocyte differentiation

9032295


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 ACVR2A (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-BH-A0BL-01AIGF2Rchr6

160390427

+ACVR2Achr2

148672760

+
ChimerDB4BRCATCGA-BH-A0BLIGF2Rchr6

160390427

+ACVR2Achr2

148672759

+
ChimerDB4BRCATCGA-BH-A0BL-01AIGF2Rchr6

160390427

+ACVR2Achr2

148672760

+
ChimerDB4BRCATCGA-BH-A0BL-01AIGF2Rchr6

160390427

-ACVR2Achr2

148672760

+


Top

Fusion Gene ORF analysis for IGF2R-ACVR2A

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-shiftENST00000356956ENST00000535787IGF2Rchr6

160390427

+ACVR2Achr2

148672760

+
Frame-shiftENST00000356956ENST00000241416IGF2Rchr6

160390427

+ACVR2Achr2

148672760

+
Frame-shiftENST00000356956ENST00000404590IGF2Rchr6

160390427

+ACVR2Achr2

148672760

+
5CDS-intronENST00000356956ENST00000495775IGF2Rchr6

160390427

+ACVR2Achr2

148672760

+
intron-3CDSENST00000475584ENST00000535787IGF2Rchr6

160390427

+ACVR2Achr2

148672760

+
intron-3CDSENST00000475584ENST00000241416IGF2Rchr6

160390427

+ACVR2Achr2

148672760

+
intron-3CDSENST00000475584ENST00000404590IGF2Rchr6

160390427

+ACVR2Achr2

148672760

+
intron-intronENST00000475584ENST00000495775IGF2Rchr6

160390427

+ACVR2Achr2

148672760

+
Frame-shiftENST00000356956ENST00000535787IGF2Rchr6

160390427

+ACVR2Achr2

148672759

+
Frame-shiftENST00000356956ENST00000241416IGF2Rchr6

160390427

+ACVR2Achr2

148672759

+
Frame-shiftENST00000356956ENST00000404590IGF2Rchr6

160390427

+ACVR2Achr2

148672759

+
5CDS-intronENST00000356956ENST00000495775IGF2Rchr6

160390427

+ACVR2Achr2

148672759

+
intron-3CDSENST00000475584ENST00000535787IGF2Rchr6

160390427

+ACVR2Achr2

148672759

+
intron-3CDSENST00000475584ENST00000241416IGF2Rchr6

160390427

+ACVR2Achr2

148672759

+
intron-3CDSENST00000475584ENST00000404590IGF2Rchr6

160390427

+ACVR2Achr2

148672759

+
intron-intronENST00000475584ENST00000495775IGF2Rchr6

160390427

+ACVR2Achr2

148672759

+

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

Top

Fusion Genomic Features for IGF2R-ACVR2A


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)
IGF2Rchr6160390427+ACVR2Achr2148672759+1.23E-050.9999877
IGF2Rchr6160390427+ACVR2Achr2148672759+1.23E-050.9999877
IGF2Rchr6160390427+ACVR2Achr2148672759+1.23E-050.9999877
IGF2Rchr6160390427+ACVR2Achr2148672759+1.23E-050.9999877

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.

Top

Fusion Protein Features for IGF2R-ACVR2A


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

ACVR2A

P27037

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}.FUNCTION: On ligand binding, forms a receptor complex consisting of two type II and two type I transmembrane serine/threonine kinases. Type II receptors phosphorylate and activate type I receptors which autophosphorylate, then bind and activate SMAD transcriptional regulators. Receptor for activin A, activin B and inhibin A. Mediates induction of adipogenesis by GDF6 (By similarity). {ECO:0000250|UniProtKB:P27038, ECO:0000269|PubMed:1314589}.

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


Top

Fusion Gene Sequence for IGF2R-ACVR2A


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.

Top

Fusion Gene PPI Analysis for IGF2R-ACVR2A


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


Top

Related Drugs for IGF2R-ACVR2A


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

Top

Related Diseases for IGF2R-ACVR2A


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
TgeneACVR2AC0920269Microsatellite Instability1CTD_human
TgeneACVR2AC1721098Replication Error Phenotype1CTD_human