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:CSMD2-IL2RA (FusionGDB2 ID:19773)

Fusion Gene Summary for CSMD2-IL2RA

check button Fusion gene summary
Fusion gene informationFusion gene name: CSMD2-IL2RA
Fusion gene ID: 19773
HgeneTgene
Gene symbol

CSMD2

IL2RA

Gene ID

114784

3559

Gene nameCUB and Sushi multiple domains 2interleukin 2 receptor subunit alpha
SynonymsdJ1007G16.1|dJ1007G16.2|dJ947L8.1CD25|IDDM10|IL2R|IMD41|TCGFR|p55
Cytomap

1p35.1

10p15.1

Type of geneprotein-codingprotein-coding
DescriptionCUB and sushi domain-containing protein 2CUB and Sushi (SCR repeat) domainCUB and sushi multiple domains protein 2interleukin-2 receptor subunit alphaIL-2 receptor subunit alphaIL-2R subunit alphaTAC antigeninterleukin 2 receptor, alpha
Modification date2020031320200322
UniProtAcc

Q7Z408

.
Ensembl transtripts involved in fusion geneENST00000373381, ENST00000373380, 
ENST00000373377, ENST00000373388, 
ENST00000489419, ENST00000338325, 
ENST00000379959, ENST00000379954, 
ENST00000256876, 
Fusion gene scores* DoF score13 X 12 X 7=10924 X 4 X 4=64
# samples 135
** MAII scorelog2(13/1092*10)=-3.0703893278914
possibly effective Gene in Pan-Cancer Fusion Genes (peGinPCFGs).
DoF>8 and MAII<0
log2(5/64*10)=-0.356143810225275
possibly effective Gene in Pan-Cancer Fusion Genes (peGinPCFGs).
DoF>8 and MAII<0
Context

PubMed: CSMD2 [Title/Abstract] AND IL2RA [Title/Abstract] AND fusion [Title/Abstract]

Most frequent breakpointCSMD2(34312485)-IL2RA(6060082), # samples:2
Anticipated loss of major functional domain due to fusion event.CSMD2-IL2RA 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 CSMD2 (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 IL2RA (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
ChimerDB4GBMTCGA-02-2486-01ACSMD2chr1

34312485

-IL2RAchr10

6060082

-
ChimerDB4GBMTCGA-02-2486-01ACSMD2chr1

34312485

-IL2RAchr10

6060082

-


Top

Fusion Gene ORF analysis for CSMD2-IL2RA

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-shiftENST00000373381ENST00000379959CSMD2chr1

34312485

-IL2RAchr10

6060082

-
Frame-shiftENST00000373381ENST00000379954CSMD2chr1

34312485

-IL2RAchr10

6060082

-
Frame-shiftENST00000373381ENST00000256876CSMD2chr1

34312485

-IL2RAchr10

6060082

-
intron-3CDSENST00000373380ENST00000379959CSMD2chr1

34312485

-IL2RAchr10

6060082

-
intron-3CDSENST00000373380ENST00000379954CSMD2chr1

34312485

-IL2RAchr10

6060082

-
intron-3CDSENST00000373380ENST00000256876CSMD2chr1

34312485

-IL2RAchr10

6060082

-
intron-3CDSENST00000373377ENST00000379959CSMD2chr1

34312485

-IL2RAchr10

6060082

-
intron-3CDSENST00000373377ENST00000379954CSMD2chr1

34312485

-IL2RAchr10

6060082

-
intron-3CDSENST00000373377ENST00000256876CSMD2chr1

34312485

-IL2RAchr10

6060082

-
intron-3CDSENST00000373388ENST00000379959CSMD2chr1

34312485

-IL2RAchr10

6060082

-
intron-3CDSENST00000373388ENST00000379954CSMD2chr1

34312485

-IL2RAchr10

6060082

-
intron-3CDSENST00000373388ENST00000256876CSMD2chr1

34312485

-IL2RAchr10

6060082

-
intron-3CDSENST00000489419ENST00000379959CSMD2chr1

34312485

-IL2RAchr10

6060082

-
intron-3CDSENST00000489419ENST00000379954CSMD2chr1

34312485

-IL2RAchr10

6060082

-
intron-3CDSENST00000489419ENST00000256876CSMD2chr1

34312485

-IL2RAchr10

6060082

-
intron-3CDSENST00000338325ENST00000379959CSMD2chr1

34312485

-IL2RAchr10

6060082

-
intron-3CDSENST00000338325ENST00000379954CSMD2chr1

34312485

-IL2RAchr10

6060082

-
intron-3CDSENST00000338325ENST00000256876CSMD2chr1

34312485

-IL2RAchr10

6060082

-

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 CSMD2-IL2RA


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.

Top

Fusion Protein Features for CSMD2-IL2RA


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
CSMD2

Q7Z408

.
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


Top

Fusion Gene Sequence for CSMD2-IL2RA


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 CSMD2-IL2RA


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 CSMD2-IL2RA


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

Top

Related Diseases for CSMD2-IL2RA


check button Diseases associated with fusion partners.
(DisGeNet 4.0)
PartnerGeneDisease IDDisease name# pubmedsSource
HgeneCSMD2C0011570Mental Depression1PSYGENET
HgeneCSMD2C0011581Depressive disorder1PSYGENET
HgeneCSMD2C0036341Schizophrenia1PSYGENET
TgeneIL2RAC0011854Diabetes Mellitus, Insulin-Dependent4CTD_human
TgeneIL2RAC0026769Multiple Sclerosis4CTD_human
TgeneIL2RAC0205734Diabetes, Autoimmune4CTD_human
TgeneIL2RAC0342302Brittle diabetes4CTD_human
TgeneIL2RAC0751324Multiple Sclerosis, Acute Fulminating4CTD_human
TgeneIL2RAC1853392Interleukin 2 Receptor, Alpha, Deficiency of4CTD_human;GENOMICS_ENGLAND;ORPHANET;UNIPROT
TgeneIL2RAC3837958Diabetes Mellitus, Ketosis-Prone4CTD_human
TgeneIL2RAC4554117Diabetes Mellitus, Sudden-Onset4CTD_human
TgeneIL2RAC0003873Rheumatoid Arthritis3CTD_human
TgeneIL2RAC0002171Alopecia Areata1CTD_human
TgeneIL2RAC0005138Berylliosis1CTD_human
TgeneIL2RAC0010346Crohn Disease1CTD_human
TgeneIL2RAC0017658Glomerulonephritis1CTD_human
TgeneIL2RAC0019693HIV Infections1CTD_human
TgeneIL2RAC0036341Schizophrenia1CTD_human
TgeneIL2RAC0041696Unipolar Depression1PSYGENET
TgeneIL2RAC0156147Crohn's disease of large bowel1CTD_human
TgeneIL2RAC0158981Neonatal diabetes mellitus1GENOMICS_ENGLAND
TgeneIL2RAC0162820Dermatitis, Allergic Contact1CTD_human
TgeneIL2RAC0267380Crohn's disease of the ileum1CTD_human
TgeneIL2RAC0345967Malignant mesothelioma1CTD_human
TgeneIL2RAC0494261Combined immunodeficiency1GENOMICS_ENGLAND
TgeneIL2RAC0678202Regional enteritis1CTD_human
TgeneIL2RAC0949272IIeocolitis1CTD_human
TgeneIL2RAC1269683Major Depressive Disorder1PSYGENET
TgeneIL2RAC1704377Bright Disease1CTD_human
TgeneIL2RAC1866040DIABETES MELLITUS, INSULIN-DEPENDENT, 101CTD_human;GENOMICS_ENGLAND
TgeneIL2RAC2350873Beryllium Disease1CTD_human
TgeneIL2RAC2700553Omenn Syndrome1GENOMICS_ENGLAND
TgeneIL2RAC2931171Juvenile pauciarticular chronic arthritis1ORPHANET
TgeneIL2RAC4505456HIV Coinfection1CTD_human