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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:ADAM9-ERCC8 (FusionGDB2 ID:2015)

Fusion Gene Summary for ADAM9-ERCC8

check button Fusion gene summary
Fusion gene informationFusion gene name: ADAM9-ERCC8
Fusion gene ID: 2015
HgeneTgene
Gene symbol

ADAM9

ERCC8

Gene ID

8754

1161

Gene nameADAM metallopeptidase domain 9ERCC excision repair 8, CSA ubiquitin ligase complex subunit
SynonymsCORD9|MCMP|MDC9|MltngCKN1|CSA|UVSS2
Cytomap

8p11.22

5q12.1

Type of geneprotein-codingprotein-coding
Descriptiondisintegrin and metalloproteinase domain-containing protein 9ADAM metallopeptidase domain 9 (meltrin gamma)cellular disintegrin-related proteincone rod dystrophy 9metalloprotease/disintegrin/cysteine-rich protein 9myeloma cell metalloproteinaseDNA excision repair protein ERCC-8Cockayne syndrome WD-repeat protein CSAcockayne syndrome WD repeat protein CSAexcision repair cross-complementation group 8excision repair cross-complementing rodent repair deficiency, complementation group 8
Modification date2020031320200322
UniProtAcc

Q13443

Q13216

Ensembl transtripts involved in fusion geneENST00000487273, ENST00000466936, 
ENST00000481513, ENST00000484143, 
ENST00000265038, ENST00000426742, 
ENST00000543101, ENST00000462279, 
Fusion gene scores* DoF score27 X 19 X 12=61568 X 8 X 7=448
# samples 3113
** MAII scorelog2(31/6156*10)=-4.31165311105397
possibly effective Gene in Pan-Cancer Fusion Genes (peGinPCFGs).
DoF>8 and MAII<0
log2(13/448*10)=-1.78498710902915
possibly effective Gene in Pan-Cancer Fusion Genes (peGinPCFGs).
DoF>8 and MAII<0
Context

PubMed: ADAM9 [Title/Abstract] AND ERCC8 [Title/Abstract] AND fusion [Title/Abstract]

Most frequent breakpointADAM9(38948865)-ERCC8(60224786), # 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
HgeneADAM9

GO:0000186

activation of MAPKK activity

17704059

HgeneADAM9

GO:0006509

membrane protein ectodomain proteolysis

9920899

HgeneADAM9

GO:0034612

response to tumor necrosis factor

11831872

HgeneADAM9

GO:0050714

positive regulation of protein secretion

17704059

TgeneERCC8

GO:0000012

single strand break repair

29545921

TgeneERCC8

GO:0000209

protein polyubiquitination

12732143

TgeneERCC8

GO:0006283

transcription-coupled nucleotide-excision repair

12732143

TgeneERCC8

GO:0006974

cellular response to DNA damage stimulus

11782547

TgeneERCC8

GO:0006979

response to oxidative stress

11782547

TgeneERCC8

GO:0009411

response to UV

12732143

TgeneERCC8

GO:0043161

proteasome-mediated ubiquitin-dependent protein catabolic process

16751180

TgeneERCC8

GO:0051865

protein autoubiquitination

12732143

TgeneERCC8

GO:0097680

double-strand break repair via classical nonhomologous end joining

29545921


check buttonFusion gene breakpoints across ADAM9 (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 ERCC8 (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
ChimerDB4HNSCTCGA-CV-A45X-01AADAM9chr8

38948865

+ERCC8chr5

60224786

-


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Fusion Gene ORF analysis for ADAM9-ERCC8

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-5UTRENST00000487273ENST00000265038ADAM9chr8

38948865

+ERCC8chr5

60224786

-
5CDS-5UTRENST00000487273ENST00000426742ADAM9chr8

38948865

+ERCC8chr5

60224786

-
5CDS-5UTRENST00000487273ENST00000543101ADAM9chr8

38948865

+ERCC8chr5

60224786

-
5CDS-intronENST00000487273ENST00000462279ADAM9chr8

38948865

+ERCC8chr5

60224786

-
intron-5UTRENST00000466936ENST00000265038ADAM9chr8

38948865

+ERCC8chr5

60224786

-
intron-5UTRENST00000466936ENST00000426742ADAM9chr8

38948865

+ERCC8chr5

60224786

-
intron-5UTRENST00000466936ENST00000543101ADAM9chr8

38948865

+ERCC8chr5

60224786

-
intron-5UTRENST00000481513ENST00000265038ADAM9chr8

38948865

+ERCC8chr5

60224786

-
intron-5UTRENST00000481513ENST00000426742ADAM9chr8

38948865

+ERCC8chr5

60224786

-
intron-5UTRENST00000481513ENST00000543101ADAM9chr8

38948865

+ERCC8chr5

60224786

-
intron-5UTRENST00000484143ENST00000265038ADAM9chr8

38948865

+ERCC8chr5

60224786

-
intron-5UTRENST00000484143ENST00000426742ADAM9chr8

38948865

+ERCC8chr5

60224786

-
intron-5UTRENST00000484143ENST00000543101ADAM9chr8

38948865

+ERCC8chr5

60224786

-
intron-intronENST00000466936ENST00000462279ADAM9chr8

38948865

+ERCC8chr5

60224786

-
intron-intronENST00000481513ENST00000462279ADAM9chr8

38948865

+ERCC8chr5

60224786

-
intron-intronENST00000484143ENST00000462279ADAM9chr8

38948865

+ERCC8chr5

60224786

-

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 ADAM9-ERCC8


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 ADAM9-ERCC8


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/:38948865/:60224786)
- 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
ADAM9

Q13443

ERCC8

Q13216

FUNCTION: Cleaves and releases a number of molecules with important roles in tumorigenesis and angiogenesis, such as TEK, KDR, EPHB4, CD40, VCAM1 and CDH5. May mediate cell-cell, cell-matrix interactions and regulate the motility of cells via interactions with integrins. {ECO:0000250|UniProtKB:Q61072}.; FUNCTION: [Isoform 2]: May act as alpha-secretase for amyloid precursor protein (APP). {ECO:0000269|PubMed:12054541}.FUNCTION: Substrate-recognition component of the CSA complex, a DCX (DDB1-CUL4-X-box) E3 ubiquitin-protein ligase complex, involved in transcription-coupled nucleotide excision repair. The CSA complex (DCX(ERCC8) complex) promotes the ubiquitination and subsequent proteasomal degradation of ERCC6 in a UV-dependent manner; ERCC6 degradation is essential for the recovery of RNA synthesis after transcription-coupled repair. It is required for the recruitment of XAB2, HMGN1 and TCEA1/TFIIS to a transcription-coupled repair complex which removes RNA polymerase II-blocking lesions from the transcribed strand of active genes. Plays a role in DNA single-strand and double-strand breaks (DSSBs) repair; involved in repair of DSSBs by non-homologous end joining (NHEJ) (PubMed:29545921). {ECO:0000269|PubMed:16751180, ECO:0000269|PubMed:16916636, ECO:0000269|PubMed:16964240, ECO:0000269|PubMed:29545921}.

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 ADAM9-ERCC8


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 ADAM9-ERCC8


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 ADAM9-ERCC8


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 ADAM9-ERCC8


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