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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:CNNM2-NOTCH4 (FusionGDB2 ID:17689)

Fusion Gene Summary for CNNM2-NOTCH4

check button Fusion gene summary
Fusion gene informationFusion gene name: CNNM2-NOTCH4
Fusion gene ID: 17689
HgeneTgene
Gene symbol

CNNM2

NOTCH4

Gene ID

54805

4855

Gene namecyclin and CBS domain divalent metal cation transport mediator 2notch receptor 4
SynonymsACDP2|HOMG6|HOMGSMRINT3
Cytomap

10q24.32

6p21.32

Type of geneprotein-codingprotein-coding
Descriptionmetal transporter CNNM2ancient conserved domain-containing protein 2cyclin M2neurogenic locus notch homolog protein 4Notch homolog 4notch 4
Modification date2020031320200327
UniProtAcc

Q9H8M5

Q99466

Ensembl transtripts involved in fusion geneENST00000369875, ENST00000369878, 
ENST00000433628, ENST00000475511, 
ENST00000383264, ENST00000425600, 
ENST00000437843, ENST00000439349, 
ENST00000443903, ENST00000454571, 
ENST00000457094, ENST00000461090, 
ENST00000465528, ENST00000487528, 
ENST00000490019, ENST00000493728, 
ENST00000495974, ENST00000375023, 
Fusion gene scores* DoF score5 X 2 X 3=302 X 2 X 2=8
# samples 52
** MAII scorelog2(5/30*10)=0.736965594166206
effective Gene in Pan-Cancer Fusion Genes (eGinPCFGs).
DoF>8 and MAII>0
log2(2/8*10)=1.32192809488736
Context

PubMed: CNNM2 [Title/Abstract] AND NOTCH4 [Title/Abstract] AND fusion [Title/Abstract]

Most frequent breakpointCNNM2(104679858)-NOTCH4(32172166), # samples:1
Anticipated loss of major functional domain due to fusion event.CNNM2-NOTCH4 seems lost the major protein functional domain in Hgene partner, which is a essential gene due to the frame-shifted ORF.
CNNM2-NOTCH4 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
TgeneNOTCH4

GO:0030879

mammary gland development

9576833


check buttonFusion gene breakpoints across CNNM2 (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 NOTCH4 (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-C8-A12Q-01ACNNM2chr10

104679858

-NOTCH4chr6

32172166

-


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Fusion Gene ORF analysis for CNNM2-NOTCH4

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
5CDS-intronENST00000369875ENST00000383264CNNM2chr10

104679858

-NOTCH4chr6

32172166

-
5CDS-intronENST00000369875ENST00000425600CNNM2chr10

104679858

-NOTCH4chr6

32172166

-
5CDS-intronENST00000369875ENST00000437843CNNM2chr10

104679858

-NOTCH4chr6

32172166

-
5CDS-intronENST00000369875ENST00000439349CNNM2chr10

104679858

-NOTCH4chr6

32172166

-
5CDS-intronENST00000369875ENST00000443903CNNM2chr10

104679858

-NOTCH4chr6

32172166

-
5CDS-intronENST00000369875ENST00000454571CNNM2chr10

104679858

-NOTCH4chr6

32172166

-
5CDS-intronENST00000369875ENST00000457094CNNM2chr10

104679858

-NOTCH4chr6

32172166

-
5CDS-intronENST00000369875ENST00000461090CNNM2chr10

104679858

-NOTCH4chr6

32172166

-
5CDS-intronENST00000369875ENST00000465528CNNM2chr10

104679858

-NOTCH4chr6

32172166

-
5CDS-intronENST00000369875ENST00000487528CNNM2chr10

104679858

-NOTCH4chr6

32172166

-
5CDS-intronENST00000369875ENST00000490019CNNM2chr10

104679858

-NOTCH4chr6

32172166

-
5CDS-intronENST00000369875ENST00000493728CNNM2chr10

104679858

-NOTCH4chr6

32172166

-
5CDS-intronENST00000369875ENST00000495974CNNM2chr10

104679858

-NOTCH4chr6

32172166

-
5CDS-intronENST00000369878ENST00000383264CNNM2chr10

104679858

-NOTCH4chr6

32172166

-
5CDS-intronENST00000369878ENST00000425600CNNM2chr10

104679858

-NOTCH4chr6

32172166

-
5CDS-intronENST00000369878ENST00000437843CNNM2chr10

104679858

-NOTCH4chr6

32172166

-
5CDS-intronENST00000369878ENST00000439349CNNM2chr10

104679858

-NOTCH4chr6

32172166

-
5CDS-intronENST00000369878ENST00000443903CNNM2chr10

104679858

-NOTCH4chr6

32172166

-
5CDS-intronENST00000369878ENST00000454571CNNM2chr10

104679858

-NOTCH4chr6

32172166

-
5CDS-intronENST00000369878ENST00000457094CNNM2chr10

104679858

-NOTCH4chr6

32172166

-
5CDS-intronENST00000369878ENST00000461090CNNM2chr10

104679858

-NOTCH4chr6

32172166

-
5CDS-intronENST00000369878ENST00000465528CNNM2chr10

104679858

-NOTCH4chr6

32172166

-
5CDS-intronENST00000369878ENST00000487528CNNM2chr10

104679858

-NOTCH4chr6

32172166

-
5CDS-intronENST00000369878ENST00000490019CNNM2chr10

104679858

-NOTCH4chr6

32172166

-
5CDS-intronENST00000369878ENST00000493728CNNM2chr10

104679858

-NOTCH4chr6

32172166

-
5CDS-intronENST00000369878ENST00000495974CNNM2chr10

104679858

-NOTCH4chr6

32172166

-
5CDS-intronENST00000433628ENST00000383264CNNM2chr10

104679858

-NOTCH4chr6

32172166

-
5CDS-intronENST00000433628ENST00000425600CNNM2chr10

104679858

-NOTCH4chr6

32172166

-
5CDS-intronENST00000433628ENST00000437843CNNM2chr10

104679858

-NOTCH4chr6

32172166

-
5CDS-intronENST00000433628ENST00000439349CNNM2chr10

104679858

-NOTCH4chr6

32172166

-
5CDS-intronENST00000433628ENST00000443903CNNM2chr10

104679858

-NOTCH4chr6

32172166

-
5CDS-intronENST00000433628ENST00000454571CNNM2chr10

104679858

-NOTCH4chr6

32172166

-
5CDS-intronENST00000433628ENST00000457094CNNM2chr10

104679858

-NOTCH4chr6

32172166

-
5CDS-intronENST00000433628ENST00000461090CNNM2chr10

104679858

-NOTCH4chr6

32172166

-
5CDS-intronENST00000433628ENST00000465528CNNM2chr10

104679858

-NOTCH4chr6

32172166

-
5CDS-intronENST00000433628ENST00000487528CNNM2chr10

104679858

-NOTCH4chr6

32172166

-
5CDS-intronENST00000433628ENST00000490019CNNM2chr10

104679858

-NOTCH4chr6

32172166

-
5CDS-intronENST00000433628ENST00000493728CNNM2chr10

104679858

-NOTCH4chr6

32172166

-
5CDS-intronENST00000433628ENST00000495974CNNM2chr10

104679858

-NOTCH4chr6

32172166

-
Frame-shiftENST00000369875ENST00000375023CNNM2chr10

104679858

-NOTCH4chr6

32172166

-
Frame-shiftENST00000369878ENST00000375023CNNM2chr10

104679858

-NOTCH4chr6

32172166

-
Frame-shiftENST00000433628ENST00000375023CNNM2chr10

104679858

-NOTCH4chr6

32172166

-
intron-3CDSENST00000475511ENST00000375023CNNM2chr10

104679858

-NOTCH4chr6

32172166

-
intron-intronENST00000475511ENST00000383264CNNM2chr10

104679858

-NOTCH4chr6

32172166

-
intron-intronENST00000475511ENST00000425600CNNM2chr10

104679858

-NOTCH4chr6

32172166

-
intron-intronENST00000475511ENST00000437843CNNM2chr10

104679858

-NOTCH4chr6

32172166

-
intron-intronENST00000475511ENST00000439349CNNM2chr10

104679858

-NOTCH4chr6

32172166

-
intron-intronENST00000475511ENST00000443903CNNM2chr10

104679858

-NOTCH4chr6

32172166

-
intron-intronENST00000475511ENST00000454571CNNM2chr10

104679858

-NOTCH4chr6

32172166

-
intron-intronENST00000475511ENST00000457094CNNM2chr10

104679858

-NOTCH4chr6

32172166

-
intron-intronENST00000475511ENST00000461090CNNM2chr10

104679858

-NOTCH4chr6

32172166

-
intron-intronENST00000475511ENST00000465528CNNM2chr10

104679858

-NOTCH4chr6

32172166

-
intron-intronENST00000475511ENST00000487528CNNM2chr10

104679858

-NOTCH4chr6

32172166

-
intron-intronENST00000475511ENST00000490019CNNM2chr10

104679858

-NOTCH4chr6

32172166

-
intron-intronENST00000475511ENST00000493728CNNM2chr10

104679858

-NOTCH4chr6

32172166

-
intron-intronENST00000475511ENST00000495974CNNM2chr10

104679858

-NOTCH4chr6

32172166

-

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 CNNM2-NOTCH4


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 CNNM2-NOTCH4


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/:104679858/:32172166)
- 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
CNNM2

Q9H8M5

NOTCH4

Q99466

FUNCTION: Divalent metal cation transporter. Mediates transport of divalent metal cations in an order of Mg(2+) > Co(2+) > Mn(2+) > Sr(2+) > Ba(2+) > Cu(2+) > Fe(2+) (By similarity). {ECO:0000250|UniProtKB:Q3TWN3}.FUNCTION: Functions as a receptor for membrane-bound ligands Jagged1, Jagged2 and Delta1 to regulate cell-fate determination. Upon ligand activation through the released notch intracellular domain (NICD) it forms a transcriptional activator complex with RBPJ/RBPSUH and activates genes of the enhancer of split locus. Affects the implementation of differentiation, proliferation and apoptotic programs. May regulate branching morphogenesis in the developing vascular system (By similarity). {ECO:0000250}.

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 CNNM2-NOTCH4


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 CNNM2-NOTCH4


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 CNNM2-NOTCH4


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

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Related Diseases for CNNM2-NOTCH4


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