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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:COL16A1-ATF7IP (FusionGDB2 ID:18077)

Fusion Gene Summary for COL16A1-ATF7IP

check button Fusion gene summary
Fusion gene informationFusion gene name: COL16A1-ATF7IP
Fusion gene ID: 18077
HgeneTgene
Gene symbol

COL16A1

ATF7IP

Gene ID

1307

55729

Gene namecollagen type XVI alpha 1 chainactivating transcription factor 7 interacting protein
Synonyms447AA|FP1572AM|ATF-IP|MCAF|MCAF1|p621
Cytomap

1p35.2

12p13.1

Type of geneprotein-codingprotein-coding
Descriptioncollagen alpha-1(XVI) chainalpha 1 type XVI collagencollagen XVI, alpha-1 polypeptidecollagen, type XVI, alpha 1activating transcription factor 7-interacting protein 1ATF-interacting proteinATF7-interacting proteinATFa-associated modulatorMBD1-containing chromatin-associated factor 1
Modification date2020031320200313
UniProtAcc

Q07092

Q5U623

Ensembl transtripts involved in fusion geneENST00000271069, ENST00000373672, 
ENST00000373668, ENST00000461217, 
ENST00000541654, ENST00000261168, 
ENST00000536444, ENST00000540793, 
ENST00000543189, ENST00000544627, 
Fusion gene scores* DoF score5 X 6 X 5=15010 X 11 X 6=660
# samples 614
** MAII scorelog2(6/150*10)=-1.32192809488736
possibly effective Gene in Pan-Cancer Fusion Genes (peGinPCFGs).
DoF>8 and MAII<0
log2(14/660*10)=-2.23703919730085
possibly effective Gene in Pan-Cancer Fusion Genes (peGinPCFGs).
DoF>8 and MAII<0
Context

PubMed: COL16A1 [Title/Abstract] AND ATF7IP [Title/Abstract] AND fusion [Title/Abstract]

Most frequent breakpointCOL16A1(32130773)-ATF7IP(14576843), # samples:3
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
HgeneCOL16A1

GO:0007155

cell adhesion

16754661

HgeneCOL16A1

GO:0033622

integrin activation

16754661

HgeneCOL16A1

GO:0033627

cell adhesion mediated by integrin

16754661

HgeneCOL16A1

GO:0051894

positive regulation of focal adhesion assembly

24466237

TgeneATF7IP

GO:0006306

DNA methylation

12665582

TgeneATF7IP

GO:0045892

negative regulation of transcription, DNA-templated

12665582

TgeneATF7IP

GO:0045893

positive regulation of transcription, DNA-templated

12665582

TgeneATF7IP

GO:0045898

regulation of RNA polymerase II transcriptional preinitiation complex assembly

12665582


check buttonFusion gene breakpoints across COL16A1 (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 ATF7IP (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-AR-A2LR-01ACOL16A1chr1

32130773

-ATF7IPchr12

14576843

+


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Fusion Gene ORF analysis for COL16A1-ATF7IP

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-3UTRENST00000271069ENST00000541654COL16A1chr1

32130773

-ATF7IPchr12

14576843

+
5CDS-3UTRENST00000373672ENST00000541654COL16A1chr1

32130773

-ATF7IPchr12

14576843

+
5CDS-5UTRENST00000271069ENST00000261168COL16A1chr1

32130773

-ATF7IPchr12

14576843

+
5CDS-5UTRENST00000271069ENST00000536444COL16A1chr1

32130773

-ATF7IPchr12

14576843

+
5CDS-5UTRENST00000271069ENST00000540793COL16A1chr1

32130773

-ATF7IPchr12

14576843

+
5CDS-5UTRENST00000271069ENST00000543189COL16A1chr1

32130773

-ATF7IPchr12

14576843

+
5CDS-5UTRENST00000271069ENST00000544627COL16A1chr1

32130773

-ATF7IPchr12

14576843

+
5CDS-5UTRENST00000373672ENST00000261168COL16A1chr1

32130773

-ATF7IPchr12

14576843

+
5CDS-5UTRENST00000373672ENST00000536444COL16A1chr1

32130773

-ATF7IPchr12

14576843

+
5CDS-5UTRENST00000373672ENST00000540793COL16A1chr1

32130773

-ATF7IPchr12

14576843

+
5CDS-5UTRENST00000373672ENST00000543189COL16A1chr1

32130773

-ATF7IPchr12

14576843

+
5CDS-5UTRENST00000373672ENST00000544627COL16A1chr1

32130773

-ATF7IPchr12

14576843

+
intron-3UTRENST00000373668ENST00000541654COL16A1chr1

32130773

-ATF7IPchr12

14576843

+
intron-3UTRENST00000461217ENST00000541654COL16A1chr1

32130773

-ATF7IPchr12

14576843

+
intron-5UTRENST00000373668ENST00000261168COL16A1chr1

32130773

-ATF7IPchr12

14576843

+
intron-5UTRENST00000373668ENST00000536444COL16A1chr1

32130773

-ATF7IPchr12

14576843

+
intron-5UTRENST00000373668ENST00000540793COL16A1chr1

32130773

-ATF7IPchr12

14576843

+
intron-5UTRENST00000373668ENST00000543189COL16A1chr1

32130773

-ATF7IPchr12

14576843

+
intron-5UTRENST00000373668ENST00000544627COL16A1chr1

32130773

-ATF7IPchr12

14576843

+
intron-5UTRENST00000461217ENST00000261168COL16A1chr1

32130773

-ATF7IPchr12

14576843

+
intron-5UTRENST00000461217ENST00000536444COL16A1chr1

32130773

-ATF7IPchr12

14576843

+
intron-5UTRENST00000461217ENST00000540793COL16A1chr1

32130773

-ATF7IPchr12

14576843

+
intron-5UTRENST00000461217ENST00000543189COL16A1chr1

32130773

-ATF7IPchr12

14576843

+
intron-5UTRENST00000461217ENST00000544627COL16A1chr1

32130773

-ATF7IPchr12

14576843

+

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 COL16A1-ATF7IP


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)
COL16A1chr132130772-ATF7IPchr1214576842+4.50E-070.9999995
COL16A1chr132130772-ATF7IPchr1214576842+4.50E-070.9999995

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.
genomic feature of top 1%

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Fusion Protein Features for COL16A1-ATF7IP


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/:32130773/:14576843)
- 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
COL16A1

Q07092

ATF7IP

Q5U623

FUNCTION: Involved in mediating cell attachment and inducing integrin-mediated cellular reactions, such as cell spreading and alterations in cell morphology. {ECO:0000269|PubMed:16754661}.FUNCTION: Recruiter that couples transcriptional factors to general transcription apparatus and thereby modulates transcription regulation and chromatin formation. Can both act as an activator or a repressor depending on the context. Mediates MBD1-dependent transcriptional repression, probably by recruiting complexes containing SETDB1. The complex formed with MBD1 and SETDB1 represses transcription and probably couples DNA methylation and histone H3 'Lys-9' trimethylation (H3K9me3) activity (Probable). {ECO:0000305}.

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 COL16A1-ATF7IP


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 COL16A1-ATF7IP


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 COL16A1-ATF7IP


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 COL16A1-ATF7IP


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