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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:CMTM7-CMTM8 (FusionGDB2 ID:17577)

Fusion Gene Summary for CMTM7-CMTM8

check button Fusion gene summary
Fusion gene informationFusion gene name: CMTM7-CMTM8
Fusion gene ID: 17577
HgeneTgene
Gene symbol

CMTM7

CMTM8

Gene ID

112616

152189

Gene nameCKLF like MARVEL transmembrane domain containing 7CKLF like MARVEL transmembrane domain containing 8
SynonymsCKLFSF7CKLFSF8|CKLFSF8-V2
Cytomap

3p22.3

3p22.3

Type of geneprotein-codingprotein-coding
DescriptionCKLF-like MARVEL transmembrane domain-containing protein 7chemokine-like factor super family 7chemokine-like factor super family member 7 variant 2chemokine-like factor superfamily 7chemokine-like factor superfamily member 7CKLF-like MARVEL transmembrane domain-containing protein 8chemokine-like factor superfamily member 8
Modification date2020031320200313
UniProtAcc

Q96FZ5

Q8IZV2

Ensembl transtripts involved in fusion geneENST00000334983, ENST00000349718, 
ENST00000307526, ENST00000458535, 
Fusion gene scores* DoF score7 X 4 X 5=1403 X 2 X 3=18
# samples 83
** MAII scorelog2(8/140*10)=-0.807354922057604
possibly effective Gene in Pan-Cancer Fusion Genes (peGinPCFGs).
DoF>8 and MAII<0
log2(3/18*10)=0.736965594166206
effective Gene in Pan-Cancer Fusion Genes (eGinPCFGs).
DoF>8 and MAII>0
Context

PubMed: CMTM7 [Title/Abstract] AND CMTM8 [Title/Abstract] AND fusion [Title/Abstract]

Most frequent breakpointCMTM7(32433557)-CMTM8(32409364), # samples:1
Anticipated loss of major functional domain due to fusion event.
* 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 CMTM7 (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 CMTM8 (3'-gene)
* Click on the image to open the UCSC genome browser with custom track showing this image in a new window.
all structure

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
ChimerDB4BLCATCGA-XF-A9SK-01ACMTM7chr3

32433557

-CMTM8chr3

32409364

+


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Fusion Gene ORF analysis for CMTM7-CMTM8

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
In-frameENST00000334983ENST00000307526CMTM7chr3

32433557

-CMTM8chr3

32409364

+
In-frameENST00000334983ENST00000458535CMTM7chr3

32433557

-CMTM8chr3

32409364

+
In-frameENST00000349718ENST00000307526CMTM7chr3

32433557

-CMTM8chr3

32409364

+
In-frameENST00000349718ENST00000458535CMTM7chr3

32433557

-CMTM8chr3

32409364

+

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 CMTM7-CMTM8


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.
genomic feature

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 CMTM7-CMTM8


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/chr3:32433557/chr3:32409364)
- 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
CMTM7

Q96FZ5

CMTM8

Q8IZV2


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
TgeneCMTM8chr3:32433557chr3:32409364ENST0000030752614105_125107174.0TransmembraneHelical
TgeneCMTM8chr3:32433557chr3:32409364ENST0000030752614147_167107174.0TransmembraneHelical
TgeneCMTM8chr3:32433557chr3:32409364ENST0000045853503105_12549116.0TransmembraneHelical
TgeneCMTM8chr3:32433557chr3:32409364ENST0000045853503147_16749116.0TransmembraneHelical
TgeneCMTM8chr3:32433557chr3:32409364ENST000004585350370_9049116.0TransmembraneHelical

- In-frame and not-retained protein feature among the 13 regional features.
PartnerGeneHbpTbpENSTStrandBPexonTotalExonProtein feature loci*BPlociTotalLenProtein featureProtein feature note
HgeneCMTM7chr3:32433557chr3:32409364ENST00000334983-1540_16653176.0DomainMARVEL
HgeneCMTM7chr3:32433557chr3:32409364ENST00000349718-1440_16653143.0DomainMARVEL
HgeneCMTM7chr3:32433557chr3:32409364ENST00000334983-15110_13053176.0TransmembraneHelical
HgeneCMTM7chr3:32433557chr3:32409364ENST00000334983-15140_16053176.0TransmembraneHelical
HgeneCMTM7chr3:32433557chr3:32409364ENST00000334983-1543_6353176.0TransmembraneHelical
HgeneCMTM7chr3:32433557chr3:32409364ENST00000334983-1577_9753176.0TransmembraneHelical
HgeneCMTM7chr3:32433557chr3:32409364ENST00000349718-14110_13053143.0TransmembraneHelical
HgeneCMTM7chr3:32433557chr3:32409364ENST00000349718-14140_16053143.0TransmembraneHelical
HgeneCMTM7chr3:32433557chr3:32409364ENST00000349718-1443_6353143.0TransmembraneHelical
HgeneCMTM7chr3:32433557chr3:32409364ENST00000349718-1477_9753143.0TransmembraneHelical
TgeneCMTM8chr3:32433557chr3:32409364ENST000003075261436_168107174.0DomainMARVEL
TgeneCMTM8chr3:32433557chr3:32409364ENST000004585350336_16849116.0DomainMARVEL
TgeneCMTM8chr3:32433557chr3:32409364ENST000003075261440_60107174.0TransmembraneHelical
TgeneCMTM8chr3:32433557chr3:32409364ENST000003075261470_90107174.0TransmembraneHelical
TgeneCMTM8chr3:32433557chr3:32409364ENST000004585350340_6049116.0TransmembraneHelical


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Fusion Gene Sequence for CMTM7-CMTM8


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 CMTM7-CMTM8


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 CMTM7-CMTM8


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 CMTM7-CMTM8


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