UTHEALTH HOME    ABOUT SBMI    A-Z    WEBMAIL    INSIDE THE UNIVERSITY
FusionGDB Logo

Home

Download

Statistics

Examples

Help

Contact

Terms of Use

Center for Computational Systems Medicine level1
leaf

Fusion Gene Summary

leaf

Fusion Gene Sample Information

leaf

Fusion ORF Analysis

leaf

Fusion Amino Acid Sequences

leaf

Fusion Protein Functional Features

leaf

Fusion Protein-Protein Interaction

leaf

Related drugs with this fusion protein

leaf

Related disease with this fusion protein

Fusion Protein:CNOT2-ERBB3

Fusion Protein Summary

check button Fusion gene summary
Fusion partner gene informationFusion gene name: CNOT2-ERBB3
FusionPDB ID: 17732
FusionGDB2.0 ID: 17732
HgeneTgene
Gene symbol

CNOT2

ERBB3

Gene ID

4848

2065

Gene nameCCR4-NOT transcription complex subunit 2erb-b2 receptor tyrosine kinase 3
SynonymsCDC36|HSPC131|IDNADFS|NOT2|NOT2HErbB-3|FERLK|HER3|LCCS2|MDA-BF-1|c-erbB-3|c-erbB3|erbB3-S|p180-ErbB3|p45-sErbB3|p85-sErbB3
Cytomap

12q15

12q13.2

Type of geneprotein-codingprotein-coding
DescriptionCCR4-NOT transcription complex subunit 2CCR4-associated factor 2negative regulator of transcription 2receptor tyrosine-protein kinase erbB-3human epidermal growth factor receptor 3proto-oncogene-like protein c-ErbB-3tyrosine kinase-type cell surface receptor HER3v-erb-b2 avian erythroblastic leukemia viral oncogene homolog 3
Modification date2020031320200327
UniProtAcc

Q9NZN8

P21860

Ensembl transtripts involved in fusion geneENST idsENST00000229195, ENST00000418359, 
ENST00000548230, ENST00000551483, 
ENST00000411731, ENST00000549832, 
ENST00000267101, ENST00000415288, 
ENST00000450146, ENST00000553131, 
Fusion gene scores for assessment (based on all fusion genes of FusionGDB 2.0)* DoF score41 X 13 X 11=586328 X 12 X 14=4704
# samples 4628
** MAII scorelog2(46/5863*10)=-3.6719332904521
possibly effective Gene in Pan-Cancer Fusion Genes (peGinPCFGs).
DoF>8 and MAII<0
log2(28/4704*10)=-4.0703893278914
possibly effective Gene in Pan-Cancer Fusion Genes (peGinPCFGs).
DoF>8 and MAII<0
Context (manual curation of fusion genes in FusionPDB)

PubMed: CNOT2 [Title/Abstract] AND ERBB3 [Title/Abstract] AND fusion [Title/Abstract]

Most frequent breakpoint (based on all fusion genes of FusionGDB 2.0)CNOT2(70672054)-ERBB3(56493958), # samples:2
Anticipated loss of major functional domain due to fusion event.CNOT2-ERBB3 seems lost the major protein functional domain in Hgene partner, which is a CGC by not retaining the major functional domain in the partially deleted in-frame ORF.
CNOT2-ERBB3 seems lost the major protein functional domain in Hgene partner, which is a CGC by not retaining the major functional domain in the partially deleted in-frame ORF.
CNOT2-ERBB3 seems lost the major protein functional domain in Hgene partner, which is a essential gene by not retaining the major functional domain in the partially deleted in-frame ORF.
CNOT2-ERBB3 seems lost the major protein functional domain in Hgene partner, which is a essential gene by not retaining the major functional domain in the partially deleted in-frame 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
HgeneCNOT2

GO:0000122

negative regulation of transcription by RNA polymerase II

14707134|16712523

TgeneERBB3

GO:0007162

negative regulation of cell adhesion

7556068

TgeneERBB3

GO:0007165

signal transduction

10572067

TgeneERBB3

GO:0009968

negative regulation of signal transduction

11389077

TgeneERBB3

GO:0014065

phosphatidylinositol 3-kinase signaling

7556068

TgeneERBB3

GO:0042127

regulation of cell proliferation

11389077

TgeneERBB3

GO:0051048

negative regulation of secretion

10559227


check buttonFusion gene breakpoints across CNOT2 (5'-gene)
* Click on the image to open the UCSC genome browser with custom track showing this image in a new window.
all structure

check buttonFusion gene breakpoints across ERBB3 (3'-gene)
* Click on the image to open the UCSC genome browser with custom track showing this image in a new window.
all structure


Top

Fusion Gene Sample Information

check buttonFusion gene information from FusionGDB2.0.
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-06-5856-01ACNOT2chr12

70672054

+ERBB3chr12

56493958

+


Top

Fusion ORF Analysis


check buttonFusion information from ORFfinder translation from full-length transcript sequence from FusionPDB.
HenstTenstHgeneHchrHbpHstrandTgeneTchrTbpTstrandSeq length
(transcript)
BP loci
(transcript)
Predicted start
(transcript)
Predicted stop
(transcript)
Seq length
(amino acids)
ENST00000229195CNOT2chr1270672054+ENST00000267101ERBB3chr1256493958+29776275401526328
ENST00000229195CNOT2chr1270672054+ENST00000450146ERBB3chr1256493958+18466275401526328
ENST00000229195CNOT2chr1270672054+ENST00000415288ERBB3chr1256493958+18086275401526328
ENST00000229195CNOT2chr1270672054+ENST00000553131ERBB3chr1256493958+22786275401526328
ENST00000418359CNOT2chr1270672054+ENST00000267101ERBB3chr1256493958+28494994121398328
ENST00000418359CNOT2chr1270672054+ENST00000450146ERBB3chr1256493958+17184994121398328
ENST00000418359CNOT2chr1270672054+ENST00000415288ERBB3chr1256493958+16804994121398328
ENST00000418359CNOT2chr1270672054+ENST00000553131ERBB3chr1256493958+21504994121398328

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
ENST00000229195ENST00000267101CNOT2chr1270672054+ERBB3chr1256493958+0.0044129770.995587
ENST00000229195ENST00000450146CNOT2chr1270672054+ERBB3chr1256493958+0.0085793790.9914206
ENST00000229195ENST00000415288CNOT2chr1270672054+ERBB3chr1256493958+0.0086856740.99131435
ENST00000229195ENST00000553131CNOT2chr1270672054+ERBB3chr1256493958+0.0074904610.9925095
ENST00000418359ENST00000267101CNOT2chr1270672054+ERBB3chr1256493958+0.0044641060.99553585
ENST00000418359ENST00000450146CNOT2chr1270672054+ERBB3chr1256493958+0.0097170750.9902829
ENST00000418359ENST00000415288CNOT2chr1270672054+ERBB3chr1256493958+0.009638530.99036145
ENST00000418359ENST00000553131CNOT2chr1270672054+ERBB3chr1256493958+0.0076405970.99235946

Top

Fusion Amino Acid Sequences


check button For individual full-length fusion transcript sequence from FusionPDB, we ran ORFfinder and chose the longest ORF among the all predicted ones.
>FusionGDB ID_FusionGDB isoform ID_FGname_Hgene_Hchr_Hbp_Henst_Tgene_Tchr_Tbp_Tenst_length(fusion AA) seq_BP

>17732_17732_1_CNOT2-ERBB3_CNOT2_chr12_70672054_ENST00000229195_ERBB3_chr12_56493958_ENST00000267101_length(amino acids)=328AA_BP=29
MIASGTVRKGHDSMVRTDGHTLSEKRNYQSQSLLSPSSGYMPMNQGNLGESCQESAVSGSSERCPRPVSLHPMPRGCLASESSEGHVTGS
EAELQEKVSMCRSRSRSRSPRPRGDSAYHSQRHSLLTPVTPLSPPGLEEEDVNGYVMPDTHLKGTPSSREGTLSSVGLSSVLGTEEEDED
EEYEYMNRRRRHSPPHPPRPSSLEELGYEYMDVGSDLSASLGSTQSCPLHPVPIMPTAGTTPDEDYEYMNRQRDGGGPGGDYAAMGACPA

--------------------------------------------------------------

>17732_17732_2_CNOT2-ERBB3_CNOT2_chr12_70672054_ENST00000229195_ERBB3_chr12_56493958_ENST00000415288_length(amino acids)=328AA_BP=29
MIASGTVRKGHDSMVRTDGHTLSEKRNYQSQSLLSPSSGYMPMNQGNLGESCQESAVSGSSERCPRPVSLHPMPRGCLASESSEGHVTGS
EAELQEKVSMCRSRSRSRSPRPRGDSAYHSQRHSLLTPVTPLSPPGLEEEDVNGYVMPDTHLKGTPSSREGTLSSVGLSSVLGTEEEDED
EEYEYMNRRRRHSPPHPPRPSSLEELGYEYMDVGSDLSASLGSTQSCPLHPVPIMPTAGTTPDEDYEYMNRQRDGGGPGGDYAAMGACPA

--------------------------------------------------------------

>17732_17732_3_CNOT2-ERBB3_CNOT2_chr12_70672054_ENST00000229195_ERBB3_chr12_56493958_ENST00000450146_length(amino acids)=328AA_BP=29
MIASGTVRKGHDSMVRTDGHTLSEKRNYQSQSLLSPSSGYMPMNQGNLGESCQESAVSGSSERCPRPVSLHPMPRGCLASESSEGHVTGS
EAELQEKVSMCRSRSRSRSPRPRGDSAYHSQRHSLLTPVTPLSPPGLEEEDVNGYVMPDTHLKGTPSSREGTLSSVGLSSVLGTEEEDED
EEYEYMNRRRRHSPPHPPRPSSLEELGYEYMDVGSDLSASLGSTQSCPLHPVPIMPTAGTTPDEDYEYMNRQRDGGGPGGDYAAMGACPA

--------------------------------------------------------------

>17732_17732_4_CNOT2-ERBB3_CNOT2_chr12_70672054_ENST00000229195_ERBB3_chr12_56493958_ENST00000553131_length(amino acids)=328AA_BP=29
MIASGTVRKGHDSMVRTDGHTLSEKRNYQSQSLLSPSSGYMPMNQGNLGESCQESAVSGSSERCPRPVSLHPMPRGCLASESSEGHVTGS
EAELQEKVSMCRSRSRSRSPRPRGDSAYHSQRHSLLTPVTPLSPPGLEEEDVNGYVMPDTHLKGTPSSREGTLSSVGLSSVLGTEEEDED
EEYEYMNRRRRHSPPHPPRPSSLEELGYEYMDVGSDLSASLGSTQSCPLHPVPIMPTAGTTPDEDYEYMNRQRDGGGPGGDYAAMGACPA

--------------------------------------------------------------

>17732_17732_5_CNOT2-ERBB3_CNOT2_chr12_70672054_ENST00000418359_ERBB3_chr12_56493958_ENST00000267101_length(amino acids)=328AA_BP=29
MIASGTVRKGHDSMVRTDGHTLSEKRNYQSQSLLSPSSGYMPMNQGNLGESCQESAVSGSSERCPRPVSLHPMPRGCLASESSEGHVTGS
EAELQEKVSMCRSRSRSRSPRPRGDSAYHSQRHSLLTPVTPLSPPGLEEEDVNGYVMPDTHLKGTPSSREGTLSSVGLSSVLGTEEEDED
EEYEYMNRRRRHSPPHPPRPSSLEELGYEYMDVGSDLSASLGSTQSCPLHPVPIMPTAGTTPDEDYEYMNRQRDGGGPGGDYAAMGACPA

--------------------------------------------------------------

>17732_17732_6_CNOT2-ERBB3_CNOT2_chr12_70672054_ENST00000418359_ERBB3_chr12_56493958_ENST00000415288_length(amino acids)=328AA_BP=29
MIASGTVRKGHDSMVRTDGHTLSEKRNYQSQSLLSPSSGYMPMNQGNLGESCQESAVSGSSERCPRPVSLHPMPRGCLASESSEGHVTGS
EAELQEKVSMCRSRSRSRSPRPRGDSAYHSQRHSLLTPVTPLSPPGLEEEDVNGYVMPDTHLKGTPSSREGTLSSVGLSSVLGTEEEDED
EEYEYMNRRRRHSPPHPPRPSSLEELGYEYMDVGSDLSASLGSTQSCPLHPVPIMPTAGTTPDEDYEYMNRQRDGGGPGGDYAAMGACPA

--------------------------------------------------------------

>17732_17732_7_CNOT2-ERBB3_CNOT2_chr12_70672054_ENST00000418359_ERBB3_chr12_56493958_ENST00000450146_length(amino acids)=328AA_BP=29
MIASGTVRKGHDSMVRTDGHTLSEKRNYQSQSLLSPSSGYMPMNQGNLGESCQESAVSGSSERCPRPVSLHPMPRGCLASESSEGHVTGS
EAELQEKVSMCRSRSRSRSPRPRGDSAYHSQRHSLLTPVTPLSPPGLEEEDVNGYVMPDTHLKGTPSSREGTLSSVGLSSVLGTEEEDED
EEYEYMNRRRRHSPPHPPRPSSLEELGYEYMDVGSDLSASLGSTQSCPLHPVPIMPTAGTTPDEDYEYMNRQRDGGGPGGDYAAMGACPA

--------------------------------------------------------------

>17732_17732_8_CNOT2-ERBB3_CNOT2_chr12_70672054_ENST00000418359_ERBB3_chr12_56493958_ENST00000553131_length(amino acids)=328AA_BP=29
MIASGTVRKGHDSMVRTDGHTLSEKRNYQSQSLLSPSSGYMPMNQGNLGESCQESAVSGSSERCPRPVSLHPMPRGCLASESSEGHVTGS
EAELQEKVSMCRSRSRSRSPRPRGDSAYHSQRHSLLTPVTPLSPPGLEEEDVNGYVMPDTHLKGTPSSREGTLSSVGLSSVLGTEEEDED
EEYEYMNRRRRHSPPHPPRPSSLEELGYEYMDVGSDLSASLGSTQSCPLHPVPIMPTAGTTPDEDYEYMNRQRDGGGPGGDYAAMGACPA

--------------------------------------------------------------

Top

Fusion Protein Functional Features


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/chr12:70672054/chr12:56493958)
- 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
CNOT2

Q9NZN8

ERBB3

P21860

FUNCTION: Component of the CCR4-NOT complex which is one of the major cellular mRNA deadenylases and is linked to various cellular processes including bulk mRNA degradation, miRNA-mediated repression, translational repression during translational initiation and general transcription regulation. Additional complex functions may be a consequence of its influence on mRNA expression. Required for the CCR4-NOT complex structural integrity. Can repress transcription and may link the CCR4-NOT complex to transcriptional regulation; the repressive function may specifically involve the N-Cor repressor complex containing HDAC3, NCOR1 and NCOR2. Involved in the maintenance of embryonic stem (ES) cell identity. {ECO:0000269|PubMed:14707134, ECO:0000269|PubMed:16712523, ECO:0000269|PubMed:21299754, ECO:0000269|PubMed:22367759}.FUNCTION: Tyrosine-protein kinase that plays an essential role as cell surface receptor for neuregulins. Binds to neuregulin-1 (NRG1) and is activated by it; ligand-binding increases phosphorylation on tyrosine residues and promotes its association with the p85 subunit of phosphatidylinositol 3-kinase (PubMed:20682778). May also be activated by CSPG5 (PubMed:15358134). Involved in the regulation of myeloid cell differentiation (PubMed:27416908). {ECO:0000269|PubMed:15358134, ECO:0000269|PubMed:20682778, ECO:0000269|PubMed:27416908}.

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.
- Retained protein feature among the 13 regional features.
PartnerGeneHbpTbpENSTStrandBPexonTotalExonProtein feature loci*BPlociTotalLenProtein featureProtein feature note
TgeneERBB3chr12:70672054chr12:56493958ENST0000041173103709_9660184.0DomainProtein kinase
TgeneERBB3chr12:70672054chr12:56493958ENST000004501461115709_966400.0700.0DomainProtein kinase
TgeneERBB3chr12:70672054chr12:56493958ENST0000041173103715_7230184.0Nucleotide bindingNote=ATP
TgeneERBB3chr12:70672054chr12:56493958ENST0000041173103788_7900184.0Nucleotide bindingNote=ATP
TgeneERBB3chr12:70672054chr12:56493958ENST0000041173103834_8390184.0Nucleotide bindingNote=ATP
TgeneERBB3chr12:70672054chr12:56493958ENST000004501461115715_723400.0700.0Nucleotide bindingNote=ATP
TgeneERBB3chr12:70672054chr12:56493958ENST000004501461115788_790400.0700.0Nucleotide bindingNote=ATP
TgeneERBB3chr12:70672054chr12:56493958ENST000004501461115834_839400.0700.0Nucleotide bindingNote=ATP
TgeneERBB3chr12:70672054chr12:56493958ENST000004117310320_6430184.0Topological domainExtracellular
TgeneERBB3chr12:70672054chr12:56493958ENST0000041173103665_13420184.0Topological domainCytoplasmic
TgeneERBB3chr12:70672054chr12:56493958ENST000004501461115665_1342400.0700.0Topological domainCytoplasmic
TgeneERBB3chr12:70672054chr12:56493958ENST0000041173103644_6640184.0TransmembraneHelical
TgeneERBB3chr12:70672054chr12:56493958ENST000004501461115644_664400.0700.0TransmembraneHelical

- Not-retained protein feature among the 13 regional features.
PartnerGeneHbpTbpENSTStrandBPexonTotalExonProtein feature loci*BPlociTotalLenProtein featureProtein feature note
HgeneCNOT2chr12:70672054chr12:56493958ENST00000229195+216437_54016.0541.0RegionNote=Repressor domain
HgeneCNOT2chr12:70672054chr12:56493958ENST00000418359+317437_54016.0541.0RegionNote=Repressor domain
HgeneCNOT2chr12:70672054chr12:56493958ENST00000551483+17437_5400192.0RegionNote=Repressor domain
TgeneERBB3chr12:70672054chr12:56493958ENST000002671012428709_9661043.01343.0DomainProtein kinase
TgeneERBB3chr12:70672054chr12:56493958ENST000004152882529709_966984.01284.0DomainProtein kinase
TgeneERBB3chr12:70672054chr12:56493958ENST000002671012428715_7231043.01343.0Nucleotide bindingNote=ATP
TgeneERBB3chr12:70672054chr12:56493958ENST000002671012428788_7901043.01343.0Nucleotide bindingNote=ATP
TgeneERBB3chr12:70672054chr12:56493958ENST000002671012428834_8391043.01343.0Nucleotide bindingNote=ATP
TgeneERBB3chr12:70672054chr12:56493958ENST000004152882529715_723984.01284.0Nucleotide bindingNote=ATP
TgeneERBB3chr12:70672054chr12:56493958ENST000004152882529788_790984.01284.0Nucleotide bindingNote=ATP
TgeneERBB3chr12:70672054chr12:56493958ENST000004152882529834_839984.01284.0Nucleotide bindingNote=ATP
TgeneERBB3chr12:70672054chr12:56493958ENST00000267101242820_6431043.01343.0Topological domainExtracellular
TgeneERBB3chr12:70672054chr12:56493958ENST000002671012428665_13421043.01343.0Topological domainCytoplasmic
TgeneERBB3chr12:70672054chr12:56493958ENST00000415288252920_643984.01284.0Topological domainExtracellular
TgeneERBB3chr12:70672054chr12:56493958ENST000004152882529665_1342984.01284.0Topological domainCytoplasmic
TgeneERBB3chr12:70672054chr12:56493958ENST00000450146111520_643400.0700.0Topological domainExtracellular
TgeneERBB3chr12:70672054chr12:56493958ENST000002671012428644_6641043.01343.0TransmembraneHelical
TgeneERBB3chr12:70672054chr12:56493958ENST000004152882529644_664984.01284.0TransmembraneHelical


Top

Fusion Protein-Protein Interaction


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 from validated records (BIOGRID-3.4.160)
GenePPI interactors


check button Protein-protein interactors based on sequence similarity (STRING)
GeneSTRING network
CNOT2
ERBB3


check button - Retained interactions in fusion protein (protein functional feature from UniProt).
PartnerGeneHbpTbpENSTStrandBPexonTotalExonProtein feature loci*BPlociTotalLenStill interaction with


check button - Lost interactions due to fusion (protein functional feature from UniProt).
PartnerGeneHbpTbpENSTStrandBPexonTotalExonProtein feature loci*BPlociTotalLenInteraction lost with


Top

Related Drugs to CNOT2-ERBB3


check button Drugs used for this fusion-positive patient.
(Manual curation of PubMed, 04-30-2022 + MyCancerGenome)
HgeneTgeneDrugSourcePMID

Top

Related Diseases to CNOT2-ERBB3


check button Diseases that have this fusion gene.
(Manual curation of PubMed, 04-30-2022 + MyCancerGenome)
HgeneTgeneDiseaseSourcePMID

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